An Update on Sec61 Channel Functions, Mechanisms, and Related Diseases

The membrane of the endoplasmic reticulum (ER) of nucleated human cells harbors the protein translocon, which facilitates membrane integration or translocation of almost every newly synthesized polypeptide targeted to organelles of the endo- and exocytotic pathway. The translocon comprises the polypeptide-conducting Sec61 channel and several additional proteins and complexes that are permanently or transiently associated with the heterotrimeric Sec61 complex. This ensemble of proteins facilitates ER targeting of precursor polypeptides, modification of precursor polypeptides in transit through the Sec61 complex, and Sec61 channel gating, i.e., dynamic regulation of the pore forming subunit to mediate precursor transport and calcium efflux. Recently, cryoelectron tomography of translocons in native ER membrane vesicles, derived from human cell lines or patient fibroblasts, and even intact cells has given unprecedented insights into the architecture and dynamics of the native translocon and the Sec61 channel. These structural data are discussed in light of different Sec61 channel activities including ribosome receptor function, membrane insertion, and translocation of newly synthesized polypeptides as well as the putative physiological roles of the Sec61 channel as a passive ER calcium leak channel. Furthermore, the structural insights into the Sec61 channel are incorporated into an overview and update on Sec61 channel-related diseases—the Sec61 channelopathies—and novel therapeutic concepts for their treatment.

Introduction

The endoplasmic reticulum (ER) represents the largest continuous tubular membrane network within nucleated mammalian cells (Friedman and Voeltz, 2011; Figure 1). Its striking dynamics were recently demonstrated via lattice light-sheet microscopy (Valm et al., 2017). While occupying up to a third of a cell's volume at any given time, the ER managed to “scan” and explore over 97% of a cell's volume within 15 min. Not surprisingly, this high mobility allows the ER to be the organelle with the highest contact rate to other compartments of the endomembrane system, such as lipid droplets or mitochondria and, therefore, the nexus of inter-organelle tethering. Together with the size of the ER comes both an array of different functions and morphological structures. The former include lipid and steroid synthesis, calcium storage, protein transport, maturation, and proteostasis some of which are assumed to occur at distinct ER subdomains (Blobel and Dobberstein, 1975; Palade, 1975; Berridge, 2002; Brostrom and Brostrom, 2003; Clapham, 2007; Braakman and Bulleid, 2011). The latter include the nuclear envelope and the peripheral ER consisting of smooth tubular and rough sheet-like areas. Recently, advances in super-resolution imaging of live and fixed cells extended the concept of tubular and sheet-like peripheral ER domains by introducing ER matrices, densely packed ER tubular arrays, to the portfolio of ER structural domains. The combination of nanoscopic approaches revealed two features. One, the peripheral ER moves at high speeds broadly dependent on cellular energy sources. And two, many of the peripheral ER structures classically identified as sheets represent instead dense matrices of convoluted tubules (Nixon-Abell et al., 2016). In the context of the ER, rough and smooth refers to the presence or absence of membrane-associated ribosomes or polysomes on the cytosolic surface. The density of bound ribosomes is considered one driver for the formation of sheets. However, common to tubes, matrices and sheets is the lumenal distance of about 50 nm in mammalian cells most likely established by lumenal spacer proteins such as Climp-63 (Shibata et al., 2006, 2010; Schwarz and Blower, 2016). Furthermore, advances in ultrathin sectioning of electron microscopy preparations visualize ER sheets, especially juxtanuclear ones, being stacked in a parking garage like fashion with interconnecting helicoidal ramps to allow dense packing in a crowded environment of neuronal and secretory salivary gland cells (Terasaki et al., 2013; Nixon-Abell et al., 2016).

FIGURE 1

Figure 1. Collage of 3D reconstructions of mammalian mitochondria and ER, respectively. The left part of the figure represents a 3D reconstruction after live cell fluorescence imaging, following import of a green fluorescent protein into the ER and of a red fluorescent protein into the mitochondria. The plasma membrane is indicated by a dashed line; the position of the round nucleus can be estimated in the upper part of the cell void of ER and mitochondria. Typical concentrations of free calcium are given for cytosol and ER of a resting cell. The right part represents a 3D reconstruction of cellular ER after CET, on top of a slice through the respective tomogram. ER membranes are shown in yellow; 80S ribosomes are shown in blue. The collage is based on Zimmermann (2016).

The heterotrimeric Sec61 complex in the ER membrane provides the dynamic polypeptide-conducting channel, which mediates membrane insertion of most membrane proteins of organelles involved in endo- and exocytosis and translocation of all precursors of polypeptides destined for these same organelles and most precursors of secretory proteins (Görlich et al., 1992) (“transport” in Figure 2). With respect to membrane proteins, the exceptions are tail-anchored (TA) membrane proteins (reviewed by Rabu et al., 2009; Borgese and Fasana, 2011), and with respect to secretory proteins, the mechanistically completely unrelated “unconventional secretion” is the alternative mechanism and described in detail elsewhere (Nickel and Rabouille, 2009). Precursors of soluble polypeptides and membrane proteins are targeted to the Sec61 complex via their amino-terminal signal peptides or transmembrane helices either during their synthesis (termed cotranslationally) or after completion of their synthesis (termed posttranslationally) (Blobel and Dobberstein, 1975; von Heijne, 1986). Predominantly, cotranslational targeting is supposed to involve the cytosolic signal recognition particle (SRP) plus its receptor on the ER surface, SRP receptor (SR) (Table 1); posttranslational targeting can involve one of several SRP-independent targeting machineries, which typically also comprise cytosolic and ER membrane resident components and may also interact with ribosomes. Thus, there is substrate overlap and redundancy in these targeting machineries that we are only beginning to appreciate. This is described in more detail below, under the subheading “Targeting of Precursor Polypeptides to the Sec61 Complex in the Human ER membrane.”

FIGURE 2

Figure 2. Artist's depiction of cross-section through the mammalian ER with a focus on signal transduction and protein biogenesis. The non-annotated structures refer to a not yet-folded polypeptide, a natively folded protein, and an aggregate of non-native polypeptides, respectively. AMPK, AMP-activated protein kinase; IP3R, IP3-receptor; SERCA, sarcoplasmic/endoplasmic reticulum Ca²⁺ ATPase. The cartoon is based on Zimmermann (2016). See text for details.

TABLE 1

Table 1. Protein transport components and associated proteins in HeLa cells.

After their targeting to the ER, precursor polypeptides with amino-terminal signal peptides or transmembrane helices associate with the Sec61 complex via their targeting peptides and trigger opening of the Sec61 channel or gating of the Sec61 channel to the open state. The latter is supported by binding of the ribosomes to the Sec61 complexes in cotranslational transport. Some precursor polypeptides require help from auxiliary components for Sec61 channel opening, such as the membrane protein complex “translocon-associated protein” (TRAP) complex or the ER lumenal Hsp70-type molecular chaperone BiP (Fons et al., 2003; Lang et al., 2012; Schäuble et al., 2012; Sommer et al., 2013). Thus, BiP and TRAP can be seen as allosteric effectors of the Sec61 channel. Subsequently, BiP and TRAP can bind to precursor polypeptides in transit through the Sec61 channel and support their partial or complete translocation by acting as molecular ratchets. This capacity was directly demonstrated for BiP by reconstitution of transport components, originally present in an ER-derived detergent extract, into proteoliposomes and their subsequent use in cell-free transport assays. Those experiments showed that inclusion of avidin into these proteoliposomes could substitute for BiP in complete and efficient translocation of precursor polypeptides, which carried biotin-modified amino acid residues, even in the case of SRP-dependent transport (Tyedmers et al., 2003). In the case of TRAP, this was suggested by cross-linking studies employing stalled precursor polypeptides and rough ER–derived membrane vesicles, i.e., rough microsomes (Conti et al., 2015). Details are given below, under the three subheadings “Structure and Dynamics of the Human Sec61 Complex during Membrane Insertion and Translocation of Polypeptides,” “Structure and Dynamics of the Human Protein Translocon during Membrane Insertion and Translocation of Polypeptides” and “Assisted Opening of the Human Sec61 Channel for Insertion and Translocation of Polypeptides.”

In many cases, membrane insertion and translocation of polypeptides in transit are accompanied by modifications, i.e., removal of signal peptides by signal peptidase, N-glycosylation by oligosaccharyltransferase (OST), or GPI anchor attachment by GPI transamidase. Simultaneously, folding and assembly of the newly imported polypeptides begins, which involves a network of molecular chaperones in the ER lumen (reviewed by Braakman and Bulleid, 2011) (“folding” in Figure 2). The central components of this chaperone network are BiP, an ATP- and Ca²⁺-dependent Hsp70-type chaperone, plus its Hsp40-type co-chaperones (ERjs or ERdj) and nucleotide exchange factors (NEFs) (reviewed by Dudek et al., 2009; Otero et al., 2010; Melnyk et al., 2014; Table 1). Furthermore, folding can involve additional chaperones, such as the glycoprotein-specific calnexin and calreticulin, and folding catalysts, i.e., protein disulfide isomerases (PDIs) and peptidylprolyl-cis/trans-isomerases (PPIases). Eventually, native polypeptides are passed on from the ER along the secretory pathway by vesicular transport.

The term “quality control” was coined to describe the fact that only correctly folded and assembled proteins are delivered from the ER to their functional location in the cell or outside of the cell (Ellgaard and Helenius, 2003). Mis-folded polypeptides are subjected to ER-associated protein degradation (ERAD) or a specialized form of autophagy (ER-phagy) (Figure 2). ERAD can apparently involve BiP and the Sec61 complex for the export of certain mis-folded polypeptides from the ER to the cytosol for subsequent degradation by the proteasome (reviewed by Römisch, 2005). Thus, BiP and the Sec61 complex act at the crossroads of ER protein import and ERAD. In general, however, dedicated ERAD machineries that are specialized in mis-folded ER-lumenal polypeptides or membrane proteins are involved, which are described in detail elsewhere (reviewed by Bagola et al., 2011). Most recent cryo-EM data characterized Hrd1 as the protein-conducting channel for ER export of mis-folded polypeptides (Schoebel et al., 2017). ER-phagy can involve the interaction between either one of the ER membrane proteins FAM134 and Sec62 with cytosolic protein LC3 and delivers whole ER sections for degradation within lysosomes (Khaminets et al., 2015; Fumagalli et al., 2016). We note that Sec62 is also involved in ER protein import and therefore provides a link between protein transport and quality control (Lakkaraju et al., 2012; Lang et al., 2012).

Prolonged protein mis-folding triggers the unfolded protein response (UPR); when the rescue attempt by decreased protein synthesis and increased levels of ER chaperones and ERAD components is unproductive, programmed cell death (apoptosis) is initiated (reviewed by Ma and Hendershot, 2001; Zhang and Kaufman, 2004; Figure 2). Thus, UPR and activation of the “intrinsic” pathway to apoptosis represent ER resident signal transduction pathways, which initially work to protect cells from aggregation-prone polypeptides. Ultimately they secure survival of the multicellular organism by sacrificing cells with terminal protein aggregation problems. The major players in UPR are the ER membrane proteins ATF6, IRE1, PERK, and Sig-1R. These are similar to the membrane-integrated ERjs in being transmembrane proteins and comprising a lumenal domain that can interact with BiP. In brief, these signal transduction components are inactive when BiP is bound to the lumenal domain; when BiP becomes sequestered by unfolded polypeptides, however, it is released and the signal transduction components become activated. Interestingly, IRE1 also interacts with the Sec61 complex, which adds yet another layer of UPR regulation and provides a noteworthy interconnection between ER protein import and ER stress signaling (Sundaram et al., 2017). A more detailed picture about BiP and ERjs is given in the section below titled “BiP and Its Co-factors in the Human ER, a Prolog” as well as the paragraphs concerning the assisted opening and closing of the Sec61 complex and “Novel Concept for Physiologic Roles of the Human Sec61 Channel in Cellular Calcium Homeostasis and Energy Metabolism.”

Induction of the intrinsic apoptosis pathway involves Ca²⁺ release from the ER, which may represent one potential physiological role of the passive ER Ca²⁺ leak that occurs at the level of the open Sec61 channel and is held at bay by BiP (Schäuble et al., 2012) (“Ca²⁺ signaling” in Figure 2). However, another potential role of the Sec61 complex acting in ER Ca²⁺ leakage may be related to regulation of ATP transport into the ER, which is essential for BiP activity. In any case, BiP and the Sec61 complex are also connected to intracellular Ca²⁺ signaling and cellular Ca²⁺ homeostasis. These issues are discussed below, in the sections on “Closing of the Human Sec61 Channel for Preservation of Cellular Calcium Homeostasis” and “Novel Concept for Physiologic Roles of the Human Sec61 Channel in Cellular Calcium Homeostasis and Energy Metabolism.”

We note that quality control does not occur only after membrane insertion or translocation at the level of protein folding and assembly. Proteasomes can also eliminate precursor polypeptides that were not properly targeted, which involves cytosolic protein Bag6 (Wang et al., 2011; Leznicki and High, 2012), or became stuck at the cytosolic surface of the Sec61 complex or even in transit through the Sec61 channel. The elimination option has been termed “pre-emptive quality control” by R. Hegde and involves the cytosolic ubiquitin-ligase Listerin or the ER lumenal ERj6 (Kang et al., 2006; Rutkowski et al., 2007; von der Malsburg et al., 2015). The latter option was described by M. Schuldiner as resolving translocon “clogging” and depends on the ER membrane-resident protease ZMPSTE24 (Ast et al., 2016). Interestingly, Bag6 also acts in protein targeting to the ER, and ERj6 appears to be involved in Sec61 channel closing, adding more examples to the list of pathway interconnections.

BiP and its Co-Factors in the Human ER, a Prolog

BiP was discovered and named as an immunoglobulin heavy chain binding protein for its role in immunoglobulin assembly. It is also known as glucose-regulated protein with a mass of 78 kDa (Grp78) because it is over-produced under ER stress conditions, such as glucose starvation (Haas and Wabl, 1983). BiP is the most abundant Hsp70-type molecular chaperone in the ER lumen, reaching concentrations in the millimolar range even under non-stress conditions, and depends on ATP and Ca²⁺ for its activity (reviewed by Dudek et al., 2009; Otero et al., 2010; Melnyk et al., 2014). Another, but less abundant, member of the Hsp70 family in the ER is glucose-regulated protein with a mass of 170 kDa (Grp170). BiP and Grp170 can form a stable complex. Furthermore, various other components were found to form oligomeric complexes together with BiP, such as other chaperones, folding catalysts, and ER-resident proteins with functions in either protein transport, N-glycosylation, or cellular Ca²⁺ homeostasis (reviewed by Dudek et al., 2009).

Hsp70-type molecular chaperones, such as BiP, bind reversibly to substrate polypeptides via their substrate-binding domains (SBDs) (Figure 3). Typically, BiP substrates are hydrophobic oligopeptides within loosely- or un-folded polypeptides (Flynn et al., 1991; Blond-Elguindi et al., 1993). Binding of a substrate to the SBD inhibits unproductive interactions of the polypeptide and favors productive folding and assembly, which occur concomitantly with release from BiP. In addition, BiP can regulate the activities of folded polypeptides (e.g., Sec61α). This binding and release of substrates by BiP are facilitated by interaction of its SBD and its nucleotide-binding domain (NBD). NBD-conformation and BiP's ATPase cycle are modulated by different Hsp70 interaction partners (Dudek et al., 2009; Otero et al., 2010; Melnyk et al., 2014). The ATP-bound state of BiP has a low affinity for substrate polypeptides, and the ADP-bound state has a high substrate affinity. Hsp40-type co-chaperones of the ER lumen (ERjs or ERdjs or, more systematically, DNAJs) stimulate the ATPase activity of BiP and thereby favor substrate binding. NEFs of the ER lumen stimulate the exchange of ADP for ATP and thus induce substrate release.

FIGURE 3

Figure 3. Artist's view of the Hsp70/Hsp40 chaperone network of the human ER. See text for details. The following binding characteristics (K_D) were observed for BiP binding in the presence of ATP (in μM): ERj1, 0.12; Sec63, 5; ERj3, 3.5; ERj4, 6.07; ERj5, 0.45; ERj6, 0.59; ERj7, 1.1. The cartoon and affinities are based on Schorr et al. (2015).

As we have stated in more general terms before (Dudek et al., 2009), ERjs are characterized by J-domains that allow interaction with BiP via the bottom of its NBD. As of today, there are seven different ERjs present in the ER of a human cell (Figure 3), termed ERj1 through ERj7. They can be sub-classified as either ER membrane proteins or soluble ER lumenal proteins both with the characteristic lumenal J-domain. In more detail, ERjs can be classified according to the domains they have in common with the bacterial DnaJ protein (Cheetham and Caplan, 1998; Hennessy et al., 2005). “Type-I ERjs contain four domains: an amino-terminal J-domain, a glycine–phenylalanine (G/F)-rich domain, a Zn finger or cysteine repeat domain, and a carboxy-terminal SBD (ERj3). Type-II ERjs contain three domains: an amino-terminal J-domain, a G/F-rich domain, and a carboxy-terminal SBD (ERj4). Type III ERjs contain only the J-domain and, in general, have more specialized functions as compared to type I and II ERjs. Thus, ERj3 and ERj4 can bind substrate polypeptides and deliver them to BiP, i.e., facilitate polypeptide folding.” However, the four thioredoxin domains within ERj5 and the tetratricopeptide repeat domain in ERj6 (p58^IPK) may also play a role in substrate binding. In addition, recent evidence provided further insight into the functional and regulatory role of three ERjs and how they balance Ca²⁺ flux across the ER membrane. While the pair of ERj3 and ERj6 minimizes the passive Ca²⁺ efflux across the Sec61 complex, ERj5 triggers the influx of Ca²⁺ via activation of the SERCA2 pump in a Ca²⁺ dependent manner (Schorr et al., 2015; Ushioda et al., 2016). Once Ca²⁺ levels in the ER are replenished, ERj5 is inactivated and forms oligomers. Interestingly, this circuit of Ca²⁺ flux across the ER membrane orchestrated by SERCA2 and the Sec61 complex is tightly connected to the master regulator of the UPR, BiP. On the one hand, direct binding of BiP to the lumenal loop 7 of the mammalian Sec61 complex prevents the leakage of Ca²⁺ (Schäuble et al., 2012). On the other hand, BiP, potentially in its function as classical chaperone, prevents oligomerization of ERj5 and, hence, inactivation of SERCA2 mediated Ca²⁺ influx (Ushioda et al., 2016). At a first glance, BiP seems to fine tune Ca²⁺ flux across the ER membrane. Yet, from a broader perspective, this circuitry sheds light on a potential connection between the Ca²⁺ balance of the ER and the UPR. Consequently, the passive Ca²⁺ efflux of the ER membrane might actually represent a signaling pathway reporting about protein homeostasis and folding capacity within the ER lumen.

Two NEFs are present in the ER lumen, Sil1 and Grp170 (Figure 3). Sil1 was predicted to be structurally related to cytosolic HspBP1, one of the NEFs of cytosolic Hsc70 in eukaryotes. Grp170 appears to be structurally related to Hsp110, an alternative NEF of cytosolic Hsc70 in eukaryotes. The structures of HspBP1 and Hsp110 suggested distinct interacting surfaces of their ER-lumenal equivalents with the top of BiP's NBD (reviewed by Bracher and Verghese, 2015).

Targeting of Precursor Polypeptides to the Sec61 Complex in the Human ER Membrane

A first concept for protein targeting to the ER was established by Blobel and Dobberstein (1975). In brief, an amino-terminal signal peptide in the nascent precursor polypeptide is recognized and bound by SRP in the cytosol and mediates a translational attenuation (Walter and Blobel, 1981; Halic et al., 2004, 2006; Voorhees and Hegde, 2015). The corresponding ribosome-nascent chain-SRP complex associates with the ER membrane via the heterodimeric SR, which is membrane anchored via the β-subunit (Meyer and Dobberstein, 1980; Gilmore et al., 1982; Miller et al., 1995). Interaction between SRP and SR drives the mutual hydrolysis of bound GTP and leads to release of the ribosome-nascent chain complex at the ER membrane in the vicinity of the Sec61 complex (Supplementary Video 1). Thus, in addition to its role in targeting precursor polypeptides to the ER, SRP is a molecular chaperone for nascent precursor polypeptides and an mRNA-targeting device. Interestingly, it also targets XBP1 mRNA to the ER, where XBP1 mRNA is cleaved by Sec61 complex associated Ire1, providing a link between ER protein import and the Ire1 branch of the UPR (Plumb et al., 2015; Kanda et al., 2016). A stalling element encoded in the 3′ region of the unspliced mRNA of XBP1 (XBP1u) leads to translational pausing after synthesis of a hydrophobic region and its emergence from the ribosomal tunnel exit (Yanagitani et al., 2011). The artifice, this mildly hydrophobic region paired with the translational arrest are allowing for unconventional SRP-mediated targeting to the Sec61 translocon, yet, avoiding efficient insertion into the ER membrane. Taking the interaction of Ire1α and the Sec61 complex into account targeting of XBP1u mRNA to the translocon allows efficient processing of XBP1u by Ire1α during ER stress conditions.

Besides SRP mediated targeting, bioinformatic analysis of the yeast secretome predicted up to 30% of all extracellular proteins being independent of SRP (Aviram and Schuldiner, 2014). Experimental identification of precursor proteins with the ability to facilitate ER targeting independent of SRP—such as GPI-anchored membrane proteins in yeast, TA membrane proteins in yeast and mammalian cells, and small presecretory proteins in the mammalian system—support the existence of alternative ER targeting machineries (Schlenstedt et al., 1990; Kutay et al., 1995; Ast et al., 2013). Accordingly, many studies determined the capacity of the ER handling a broad variety of structurally diverse precursor proteins (Stefanovic and Hegde, 2007; Schuldiner et al., 2008; Aviram et al., 2016). Their diversity is not restricted to differences in the amino acid sequence of matures domains, but equally evident in primary structure, length, hydrophobicity and location of the signal sequence itself (reviewed by von Heijne, 1985; Hegde and Bernstein, 2006). Although each of these signal sequence features has been addressed experimentally to demonstrate impact on the targeting process, the location of the targeting peptide within the precursor protein is what led to the identification of the first SRP-independent targeting route for TA membrane proteins.

TA proteins are classically defined as single spanning type 2 membrane proteins devoid of a cleavable signal sequence. Instead, TA proteins harbor a characteristic carboxy-terminally located transmembrane helix, the tail-anchor (Kutay et al., 1995; Rabu et al., 2009; Borgese and Fasana, 2011). Roughly 1% of the human genome encodes TA proteins, not all of which end up in membranes of the endo- or exocytotic pathways. TA proteins of the secretory pathway, such as the β- and γ-subunits of the Sec61 complex, Cytochrome b₅, and many components of vesicular transport, need to be targeted and inserted into the ER membrane. Equivalent to the underlying principle of the SRP-mediated targeting, TA proteins are chaperoned in a translocation-competent fashion through the cytosol and directed to the ER membrane via an ER membrane resident receptor complex. The minimal targeting machinery for TA proteins was termed the guided entry of tail-anchored proteins (GET)-complex in yeast and TA receptor complex (TRC) in the mammalian system (Table 1). In principle, the cytosolic ATPase Trc40 with its hydrophobic binding pocket binds the TA protein, and the heterodimeric receptor complex, comprising Wrb and Caml, is required for efficient ER targeting (Stefanovic and Hegde, 2007; Vilardi et al., 2011, 2014; Yamamoto and Sakisaka, 2012). At least in yeast, orthologs of the latter two proteins are also supposed to facilitate the actual TA membrane insertion (Wang et al., 2011). Furthermore, the mammalian TA-targeting machinery involves a ribosome-associating heterotrimeric Bag6 complex (comprising Bag6, Ubl4A, and Trc35) and SGTA, which appear to act upstream of Trc40 (Leznicki et al., 2010; Mariappan et al., 2010). Interestingly, Bag6 is also involved in degradation of TA proteins, i.e., at the crossroads of targeting and quality control (Wang et al., 2011; Leznicki and High, 2012).

Although about one dozen genes encoding for yeast TA proteins were characterized as essential, knockout strains of the yeast GET machinery were viable, suggesting the existence of at least one alternative targeting route. Indeed, in 2016, a high-throughput screening approach in the lab of M. Schuldiner identified a hitherto uncharacterized targeting pathway in yeast, termed the SRP-independent (SND)-system (Aviram et al., 2016). This genetic screen used a fluorescent reporter substrate based on an obligate SRP-independent and only partially GET-dependent substrate protein. Hence, mislocalization of this reporter in any particular null mutant strain served as evidence of a targeting factor. Three novel components have been identified and characterized: Snd1, Snd2, and Snd3 (Table 1). Two hallmarks of the SND targeting pathway have been emphasized. First, similar to the SRP- and GET-targeting mechanisms, precursor substrates were targeted via the interplay of a cytosolic mediator (Snd1) and a heterodimeric receptor located at the ER membrane (Snd2, Snd3). We note that Snd1 had previously been described as a ribosome-interacting protein. Second, the SND machinery showed a preference for substrates with a central transmembrane domain. At the same time, the SND route could provide an alternative targeting pathway for substrates with a transmembrane helix at their extreme amino- or carboxy-terminus, i.e., typical SRP- or GET-dependent substrates. So far, no nucleotide requirement has been assigned to this targeting system. Sequence comparisons identified the previously characterized ER membrane protein TMEM208 as a putative human Snd2 orthologue, termed hSnd2 (Zhao et al., 2013; Aviram et al., 2016). According to experiments that combined siRNA-mediated gene silencing and protein transport into the ER of human cells in cell-free transport assays, hSnd2 appears to have the same function as its yeast counterpart (Haßdenteufel et al., 2017). So far, however, human orthologs of Snd1 and Snd3 have not been identified. Judging from the levels of SR, Wrb/Caml, and hSnd2 in HeLa cells, the impression is that the SND pathway may account for almost 30% of precursor targeting in this particular human cell (Hein et al., 2015; Table 1). Interestingly, TMEM208 was originally described as a player in ER-phagy, providing yet another link between ER protein import and protein quality control (Zhao et al., 2013).

In addition, fully synthesized precursors of small presecretory proteins in human cells were proposed to be targeted to the mammalian ER membrane in an SRP-independent fashion in several ways: (i) by their interaction with Trc40 and its putative interaction with the Trc40 receptor, (ii) by their interaction with the cytosolic protein calmodulin and its putative association with a calmodulin-binding IQ motif in the cytosolic amino-terminus of the Sec61α protein, and (iii) by direct interaction of their signal peptides with the ER membrane resident Sec62 (Shao and Hegde, 2011; Johnson et al., 2012, 2013; Lakkaraju et al., 2012). In the latter case, precursors may be chaperoned in the cytosol by Hsc70 and its Hsp40 type co-chaperones or by calmodulin, if or when the latter does not act in targeting via the IQ motif. In terms of interconnections between pathways, it is interesting to note that calmodulin was described to inhibit rather than stimulate targeting of TA proteins to the mammalian ER membrane (Haßdenteufel et al., 2011). Along the same lines, the Hsc70-interacting protein Bag1 can also deliver proteins to the proteasome, i.e., acts at the cross-roads of targeting and quality control (Alberti et al., 2003), and Sec62 can facilitate ER-phagy (Fumagalli et al., 2016).

Furthermore, the synthesis of many polypeptides is apparently initiated on ribosomes or large ribosomal subunits that are continuously attached to the ER membrane (Potter et al., 2001; Stephens et al., 2008). Therefore, direct mRNA targeting was suggested as an alternative ER-targeting mechanism, and the proteins p180 and kinectin were described as mRNA receptors in the ER membrane (Table 1). So far, there is no consensus about the possible specificity of this targeting reaction, and we are not aware of a single example of a precursor polypeptide in which mRNA targeting was a prerequisite for subsequent membrane insertion or translocation by the Sec61 complex. However, polypeptides that lack a signal peptide for ER targeting and whose synthesis was initiated on ER-bound ribosomes or large ribosomal subunits were found to be recognized by the nascent chain associated complex (NAC) (Wiedmann et al., 1994). Apparently, this interaction leads to release of the respective ribosomes from the membrane and completion of protein synthesis in the cytosol (Möeller et al., 1998; Gamerdinger et al., 2015). Thus, NAC-mediated targeting antagonism keeps the intrinsic affinity of ribosome-nascent chain complexes for the Sec61 complex in check and thereby prevents both extensive mistargeting of mitochondrial proteins to the ER and impairment of protein homeostasis in those organelles.

From a broader perspective, the emerging concept for ER protein targeting is that a molecular triage is occurring for ER-destined precursor polypeptides in the cytosol, determining the fates of nascent or fully synthesized but not-yet-folded polypeptides. It does so via a complex network of targeting signals in nascent chains and completed polypeptides and a whole variety of cytosolic factors that decode these signals. At first, these factors assist the precursors in staying in solution and remaining competent for ER targeting as well as subsequent insertion into or translocation across the ER membrane. If one of these tasks fails, the precursor is targeted to the proteasome. At later stages of protein biogenesis at the ER, this principle is repeated at the level of membrane insertion and translocation and eventually during folding and assembly.

Structure and Dynamics of the Human Sec61 Complex during Membrane Insertion and Translocation of Polypeptides

From a historical perspective the term “Sec” was allocated to proteins involved in protein “sec”retion and first introduced based on a yeast screen from the Schekman lab for mutants unable to efficiently secrete invertase and acid phosphatase (Novick et al., 1980; Spang, 2015). Although not among the initial 23 complementation groups, Sec61 was identified in a follow-up study also by the Schekman group (Deshaies and Schekman, 1987; Schekman, 2002). Subsequently, the structure of the hetero-trimeric Sec61 complex was first suggested by T. Rapoport and colleagues based on the X-ray crystallographic analysis of isolated archaean ortholog SecY complex (Van den Berg et al., 2004). The high sequence conservation of the SecY and Sec61 subunits indicated that their architecture and dynamics are evolutionarily conserved, which was confirmed by a number of subsequent cryo-electron microscopy (EM)-studies on detergent-solubilized or reconstituted ribosome-bound SecY or Sec61 complexes (Gogala et al., 2014; Voorhees et al., 2014). The central channel-forming subunit (Sec61α) consists of 10 transmembrane helices and is arranged in two pseudo-symmetrical amino- and carboxy-terminal halves around a central constriction which is sealed by the “pore ring,” a ring of bulky hydrophobic side chains, and a short “plug” helix (Figures 4, 5). The Sec61β and Sec61γ subunits are present on the outskirts of the Sec61 complex and contain one TA each. Strikingly, two distinct conformations of the Sec61 channel could be distinguished, which differ in the relative positioning of the amino- and carboxy-terminal Sec61α halves. These conformations either allow or don't allow lateral access of signal peptides or transmembrane helices of polypeptides in transit from the central channel toward the phospholipid bilayer through a “lateral gate” formed by transmembrane helices 2 and 7 of Sec61α (Figures 4, 5). This “lateral gate” enables insertion of nascent transmembrane helices or signal peptides emerging from the ribosome into the phospholipid bilayer. Without doubt, events at the “lateral gate” of the Sec61 complex are critical for understanding the process of protein translocation under physiological conditions, i.e., allowing transfer of a proteinaceous entity from one environment into a very different second one and simultaneously preserving the steep ER to cytosol Ca²⁺ gradient in the cell. Structural determination of programmed ribosome-Sec61 complexes implied a series of events upon arrival of a nascent precursor (Voorhees et al., 2014; Voorhees and Hegde, 2016). The idle or quiescent Sec61 complex unable to promote protein transfer is primed by binding of the ribosome to cytosolic loops 6 and 8 of Sec61α as well as the amino-terminus of Sec61γ, unveiling a hydrophobic patch in the cytosolic funnel of the engaged Sec61 complex (Figures 5, 6). This patch, in vicinity to the lateral gate, serves as an interaction site for an incoming hydrophobic signal peptide that in turn displaces helix 2 of Sec61α in order to destabilize the “lateral gate” and open the aqueous channel in the Sec61 complex for protein translocation. The cryo-EM data also demonstrated that even in cotranslational translocation, some considerable stretch of a nascent precursor polypeptide can accumulate at the interface between the ribosome and the Sec61 complex without compromising translocation (Park et al., 2014; Conti et al., 2015). Thus, elongation does not necessarily provide a driving force in translocation.

FIGURE 4

Figure 4. Structure and architecture of the native mammalian translocon visualized using CET. (Left) Overall structure of the native ribosome-translocon complex (EMD 3069) with the ribosomal subunits (40S: yellow; 60S: light blue) and the translocon components Sec61 (dark blue), TRAP (green) and OST (red) depicted. Within the 60S subunit, eL38 (purple) and the short expansion segment (bright yellow), which are contacted by the cytosolic domain of TRAPγ, are highlighted. Right, upper panel: Isolated density for the Sec61 complex with an atomic model of the laterally opened Sec61 complex (PDB 3jc2) superposed. The Sec61α (N-terminal: green; C-terminal half: blue), Sec61β (yellow) and Sec61γ (orange) subunits are indicated. A signal peptide (magenta) is intercalated at the lateral gate. Right, lower panel: Transmembrane region of the translocon with down-filtered densities for membrane-embedded segments of TRAP (green) and OST (red) depicted. Sec61 is represented by an atomic model. The ER membrane resides in the paper plane.

FIGURE 5

Figure 5. Artist's view of the dynamic equilibrium and gating mechanisms of the human Sec61 complex. Allosteric effectors of the dynamic equilibrium of the Sec61 channel and their binding sites are indicated. The cartoon is based on Dudek et al. (2015). See text for details.

FIGURE 6

Figure 6. Artist's depiction of the domain organization of Sec61 complex and its auxiliary components BiP, Sec62, and Sec63. Additional interaction partners of BiP (Sil1), Sec61 (Calmodulin, CaM), Sec62 (LC3), and Sec63 (Nucleoredoxin, NRX; Calumenin, Calu) are shown. Furthermore, relevant motifs (such as IQ and LIR) and domains are indicated, as well as point mutations that disturb the respective interaction or are linked to disease (in red). CCD, coiled-coil domain; EF, EF hand; NBD, nucleotide-binding domain; NP, negatively charged patch; PP, positively charged patch; RBS, ribosome-binding site; SBD, substrate-binding domain. The following binding characteristics were observed: BiP/Sec61α K_d 500 μM, ATP-dependent; BiP/Sec63 K_D 5 μM; CaM/Sec61α K_D 115 nM, Ca²⁺-dependent, TFP-sensitive; Sec62/Sec61α Ca²⁺-sensitive; Sec62/LC3 K_D 20 μM; Sec63/NRX H₂O₂-dependent; Sec63/Sec62 K_D 5 nM. C, carboxy-terminus; N, amino-terminus. See text for details.

Cryoelectron tomography (CET) of translocons in native ER membrane vesicles derived from human cell lines or primary fibroblasts and even intact cells has given unprecedented insights into the architecture and dynamics of the Sec61 channel in its physiological setting and of the native translocon (Pfeffer et al., 2014, 2015, 2017; Mahamid et al., 2016). The atomic model of the solubilized ribosome-bound Sec61 complex (Voorhees et al., 2014), opened laterally by a signal peptide, was easily docked into the CET density, defining the position and conformation of Sec61 subunits in the center of the native translocon (Figure 4). Furthermore, weak helical density opposing the “lateral gate” in the CET density map confirmed the position of signal peptides, as it had been observed after detergent solubilization of ribosome-nascent chain-bound Sec61 complexes. Sec61 was found with an open “lateral gate,” possibly suggesting that Sec61 remains laterally open throughout protein translocation. At this point, the aqueous channel in the center of the complex is most likely occupied by the polypeptide chain in transit. However, computational sorting of subtomograms implied that the majority of ribosome–translocon complexes are idle and, therefore, not engaged in membrane protein insertion or protein translocation, although they were characterized by an open “lateral gate.” A possible explanation for laterally open Sec61 bound to idle ribosomes may be that even after termination of protein synthesis, signal peptides or transmembrane helices remain bound to Sec61 and keep the “lateral gate” open. In line with this view, helical density coinciding with the position of signal peptides was observed opposite of the “lateral gate” also for idle ribosome–Sec61 complexes. In this case, the aqueous channel in the center of the complex should be closed by the “pore ring” and/or the “plug” helix.

Structure and Dynamics of the Human Protein Translocon during Membrane Insertion and Translocation of Polypeptides

As we have previously outlined (Zimmermann et al., 2011), “the first hints on participation of additional components in cotranslational protein transport came from the analysis of ribosome-associated ER membrane proteins present in detergent extracts of mammalian canine pancreatic microsomes. The term ribosome-associated membrane proteins (RAMPs) was coined for this class of membrane proteins after their solubilization in the presence of 400 mM potassium chloride (Görlich and Rapoport, 1993). By definition, the Sec61 complex is a RAMP, and so are RAMP4, TRAP and OST (Table 1). More recently, ERj1 and Sec62 were characterized as RAMPs, although their ribosome association is seen only under more physiological salt concentrations (up to 200 mM potassium chloride) and therefore may be more dynamic compared with the high-salt resistant RAMPs (Blau et al., 2005; Dudek et al., 2005; Benedix et al., 2010; Müller et al., 2010).

Additional information on the composition of the native protein transport machinery in the ER membrane came from fluorescence resonance energy transfer (FRET) experiments, which employed fluorescently labeled antibodies against transport components, permeabilized canine cells, and fluorescence microscopy.” According to this more physiological experimental strategy, Sec61α1, Sec61β, Sec62, and ERj1 are RAMPs, i.e., they are associated with ribosomes in the intact ER (Snapp et al., 2004; Benedix et al., 2010; Müller et al., 2010). Furthermore, this approach demonstrated that SR, the TRAP complex, and translocating chain-associating membrane (TRAM) protein are permanently in close proximity to Sec61 complexes. Recent cross-linking data suggested that SR and Sec62 interact with Sec61α in a mutually exclusive manner and may use the same binding site at the cytosolic amino-terminus (Jadhav et al., 2015). Therefore, it was proposed that SR can switch the Sec61 channel from Sec62- to SRP-dependent translocation.

Other experiments addressing the dynamics of the human protein translocon showed that precursors of ERj3 and prion protein depend on BiP, Sec62, and Sec63 in their ER import in cell-free transport experiments (Lang et al., 2012; Schäuble et al., 2012). Additional cross-linking experiments with stalled, radiolabeled precursor polypeptides in transit through the translocon of canine pancreatic ER membranes demonstrated that Sec62 and Sec63 only transiently associate with the Sec61 complex in a substrate-specific manner (Conti et al., 2015). Both precursor polypeptides analyzed, ERj3 and prion protein, appeared to recruit Sec62 and Sec63 to the Sec61 complex rather late in their synthesis, i.e., at precursor polypeptide chain lengths of around 150 amino acid residues. And, their signal peptides become accessible to ER-lumenal signal peptidase at chain lengths of almost 200 amino acid residues. Interestingly, a similar situation, i.e., a dynamic recruitment of Sec62 and Sec63, could be forced even for preprolactin by introducing a tightly folded zinc finger domain in the presence of Zn²⁺. As would be expected based on previous cross-linking studies with nascent preprolactin chains, preprolactin was first processed by signal peptidase at a chain length of 140 residues and found in complex with Sec61 complex, TRAP, TRAM, and OST at this stage of translocation. We conclude from these observations that in contrast to preprolactin, the two precursors of ERj3 and prion protein may contain “weak” or slowly-gating signal peptides. As a result, opening of the Sec61 channel occurred late in their synthesis, and extended sections of these two precursor polypeptides accumulated at the interface between the ribosome and the Sec61 complex triggering a rearrangement of the translocon composition to facilitate precursor translocation.

We note that a permanent association of ribosome-associated Sec61 complexes with TRAP and OST was confirmed in the recent three-dimensional (3D) reconstructions after CET of native translocons in ER membrane vesicles, derived from canine pancreas or various human cells and even intact cells (Pfeffer et al., 2014, 2015, 2016; Mahamid et al., 2016; Figure 4). Interestingly, all ribosome-associated Sec61 complexes were routinely found to be associated with TRAP, irrespective of the cellular origin of the native complexes. However, the occupancy of these Sec61/TRAP super-complexes by OST varied from one cell type to the next. While the OST occupancy was found to be around 70% in dog pancreas microsomes and microsomes isolated from several other cell types specialized in protein secretion, only 35% of translocon complexes contained OST in microsomes isolated from HeLa or HEK cells and in intact HeLa cells (Pfeffer et al., 2016). So far, our efforts to locate the position of further ones of the abovementioned translocon components have not been successful. At present, only TRAM remains a candidate for permanent and stoichiometric presence in the translocon, because it does not comprise lumenal or cytosolic domains large enough for detection using CET. Therefore, it may represent the density that is consistently found opposite of the “lateral gate” in CET of native translocons (Pfeffer et al., 2012).

Mammalian TRAP is a heterotetrameric membrane protein complex, with three subunits (α, β, δ) predicted to comprise one transmembrane helix plus one lumenal domain each, while TRAPγ likely comprises a bundle of four transmembrane helices plus a cytosolic domain (Hartmann et al., 1993; Bañó-Polo et al., 2017; Pfeffer et al., 2017; Figure 7). This bundle of transmembrane helices appears to be flanking both Sec61γ and the carboxy-terminal half of Sec61α (Figures 4, 7), and the cytosolic domain seems to interact with the ribosome via ribosomal protein eL38 and a short RNA expansion segment. The heterotrimeric ER-lumenal segment of TRAP reaches across the central Sec61 channel and binds to the crucial “hinge” region between the amino- and carboxy-terminal halves of Sec61α. Within the trimeric lumenal TRAP segment, the δ-subunit contacts OST (most likely ribophorin II), and the dimer formed by the lumenal domains of α- and β- subunits contacts ER lumenal loop 5 in the “hinge” region between the amino- and carboxy-terminal halves of Sec61α. In this position, the ER lumenal domain of TRAP may be able to act in a chaperone-like fashion on the conformational state of Sec61α or as a molecular ratchet on nascent precursor polypeptides in transit into the ER lumen or both, in analogy to BiP. We note that various algorithms predict a beta sandwich fold for the ER lumenal domains of TRAP's α- and β- subunits and that TRAPα was also characterized as Ca²⁺-binding protein (Wada et al., 1991).

FIGURE 7

Figure 7. Artist's depiction of the organization of Sec61 complex and its auxiliary component TRAP. Relevant motifs (IQ) and domains are indicated, as well as point mutations that disturb the respective interaction or are linked to disease (in red). BS, binding site; OST, oligosaccharyltransferase; RBS, ribosome-binding site. C, carboxy-terminus; N, amino-terminus. See text for details.

Assisted Opening of the Human Sec61 Channel for Membrane Insertion and Translocation of Polypeptides

The current view on opening of the Sec61 complex for protein translocation, i.e., channel gating from the closed to the open conformation, is that signal peptides of nascent presecretory polypeptides intercalate between the Sec61α transmembrane helices 2 and 7, displace helix 2, and open the “lateral gate” of the Sec61 complex formed by these two transmembrane helices (Van den Berg et al., 2004; Gumbart et al., 2009; Voorhees et al., 2014; Figure 4). Actually, it has been suggested that this intercalation rather than the originally proposed displacement of the “plug” helix represents the crucial reaction in the early phase of membrane insertion of translocation, i.e., the energetic barrier for Sec61 channel opening (Figure 8). Next, the nascent chain can be fully inserted into the Sec61 channel, either in “hairpin” (where the amino-terminus of the signal peptide stays in the cytosol) or “head-first” configuration (where the amino-terminus of the signal peptide reaches into the ER lumen), and initiate translocation (Devaraneni et al., 2011; Park et al., 2014; Vermeire et al., 2014). The “hairpin” insertion is considered to represent the more productive mode whereas a “head-first” insertion has to be followed by a reversal of orientation (termed “flip turn”) to allow the sequence downstream of the signal peptide to enter the ER lumen. The latter may be considered a second energetically unfavorable reaction, typically requiring help from components, which can lower the energetic barrier for the “flip turn” (Figure 8). The idea is that some amino-terminal signal peptides or transmembrane helices may be “strong” or quickly-gating enough to trigger Sec61 channel opening quickly on their own, particularly after the ribosome has already primed the channel. However, precursor polypeptides with “weak” signal peptides appear to involve auxiliary components in Sec61 channel opening in order to facilitate insertion of precursor polypeptides into the Sec61 complex (Table 1). Alternatively, the auxiliary components may support the abovementioned “flip turn” in case of an original “head-first” insertion. Based on in vitro experiments the concept emerged that TRAP and BiP facilitate Sec61 channel opening in a substrate specific manner. In particular, precursor polypeptides with “weak” signal peptides or transmembrane helices are affected (Fons et al., 2003; Schäuble et al., 2012; Figure 5; Supplementary Video 1). Based on only a small set of model precursor polypeptides, the distinguishing factor that determines the requirement for BiP and its membrane bound co-chaperone Sec63 was suggested to be a short and rather apolar signal peptide, eventually to support it in displacing helix 2 of Sec61α on its own account. The TRAP complex was observed in in vitro transport studies to stimulate translocation of specific proteins, such as the prion protein. Recent studies in intact cells have suggested that TRAP might also affect the topology of transmembrane helices that do not promote a specific initial orientation of membrane protein precursors in the membrane (Sommer et al., 2013). As noted before (Haßdenteufel et al., 2014), several additional proteins in the mammalian ER membrane can be considered as auxiliary translocon components, most notably TRAM (Voigt et al., 1996; Hegde et al., 1998). In the case of TRAM, signal peptides of precursors with long amino-terminal as well as long hydrophobic core regions showed a low TRAM dependence in in vitro experiments. Interestingly, there is a second TRAM in mammalian cells, termed TRAM2, which can invert the topology of transmembrane helices that do not promote a specific initial orientation in the membrane (Chen et al., 2016).

FIGURE 8

Figure 8. Energetics of Sec61 channel gating. See text for details.

We suggest that certain features of signal peptides may extend the “dwell” time or “sampling” of signal peptides on the cytosolic surface of the Sec61 channel and that BiP and TRAP can overcome this by facilitating Sec61 channel gating on the lumenal side (Zhang and Miller, 2012; Van Lehn et al., 2015). This raises the exciting possibility that BiP and TRAP have overlapping specificities, i.e., that there is also redundancy in this reaction, as discussed above for the targeting reaction. Another interesting and equally open question is what features make a signal peptide or transmembrane helix “weak” or “strong” for Sec61 channel opening and if it is really only these topogenic sequences that determine this “weakness” or “strength.” Some features have already been mentioned above but were determined using only small sets of model proteins. However, our own unpublished work suggests that special features downstream of the signal peptides can also play a distinct role, which may be particularly relevant in cotranslational translocation when a considerable stretch of a nascent precursor polypeptide accumulates at the interface between ribosome and Sec61 complex, i.e., prior to Sec61 channel opening (see above) and in posttranslational translocation (S. Haßdenteufel, personal communication). This is reminiscent of the effects of downstream sequences in the integration of transmembrane helices into the membrane (Junne and Spiess, 2017). Interestingly, yeast Sec62 and mammalian TRAP were found to affect the topology of transmembrane helices that do not promote a specific initial orientation of membrane protein precursors in the membrane (Reithinger et al., 2013; Sommer et al., 2013).

In the case of BiP, it has been suggested that the minihelix within loop 7 of Sec61α plays a role in gating of the Sec61 complex from closed to open and that BiP binding to this minihelix may be required for only some precursor polypeptides (Figures 5, 6). “Thus, by providing binding energy, the ribosome and BiP may be able to ‘pull’ transmembrane helix 7 from opposite ends to facilitate channel opening (Figure 8; Schäuble et al., 2012). We find this hypothesis attractive because loop 7 connects transmembrane helices 7 and 8 and is thus close enough to the “lateral gate” to influence gate movements.” Thus, BiP together with Sec63 protein represents an allosteric effector of the Sec61 complex for channel opening. This view was supported by the observations that the murine diabetes-linked mutation of tyrosine 344 to histidine within loop 7 destroys the BiP binding site and, when introduced into HeLa cells, prevents in vitro transport of BiP-dependent, i.e., slowly-gating precursor polypeptides.

As stated above, the dimer formed by the lumenal domains of the α- and β- subunits of TRAP contacts ER lumenal loop 5 in the “hinge” region between the amino- and carboxy-terminal halves of Sec61α (Pfeffer et al., 2017; Figures 4, 7). Thereby, it may act as an alternative allosteric effector of Sec61 channel and thus may facilitate opening of the Sec61 channel to allow initiation of protein translocation and topogenesis of membrane proteins, in analogy to the action of BiP on loop 7. Therefore, the question arises of how TRAP may signal the presence of a signal peptide requiring help in Sec61 channel gating to the ER lumenal TRAP domains (see above).

Closing of the Human Sec61 Channel for Preservation of Cellular Calcium Homeostasis

As discussed before (Zimmermann, 2016), “the mammalian ER is also a central player in cellular calcium homeostasis (Figures 1, 2). It represents the major Ca²⁺ storage organelle in nucleated mammalian cells and allows controlled release of Ca²⁺ from the ER upon hormone stimulation of a resting cell, e.g., via IP3 receptor (Berridge, 2002; Clapham, 2007). Subsequently, Ca²⁺ is pumped back into the ER by sarcoplasmic/ER Ca²⁺ ATPase (SERCA) to re-establish the steep ER to cytosol Ca²⁺ gradient (Wuytack et al., 2002). This gradient is also constantly challenged by passive Ca²⁺ efflux from the ER, so SERCA has the additional task of counteracting this Ca²⁺ leakage. In addition, Ca²⁺ is taken up by mitochondria. In the course of the last 10 years, several proteins were linked to ER Ca²⁺ leakage, including the Sec61 channel (Lomax et al., 2002; Van Coppenolle et al., 2004; Erdmann et al., 2011). Other candidate proteins that were identified acting as putative Ca²⁺ permeable leak channel at the ER membrane are presenilin1 (Tu et al., 2006), Bcl2 (Chami et al., 2004), pannexin1 (Vanden Abeele et al., 2006), TRPC1 (Berbey et al., 2009), CALHM1 (Gallego-Sandín et al., 2011), and a truncated SERCA1 isoform (Chami et al., 2001, 2008). Some of those candidate proteins, however, were ruled out as passive Ca²⁺ leak channels allowing the efflux of Ca²⁺ from the ER observed in all nucleated cells. For example, presenilin was shown to have a stimulatory effect on IP3 receptors (Cheung et al., 2008, 2010), i.e., triggering a rather direct Ca²⁺ release from the ER. In addition, mature presenilin is predominantly located in the plasma and Golgi membrane (https://www.proteinatlas.org). Similarly, mature Bcl2, pannexin1, and TRPC1 are not present at the ER membrane to act as ubiquitous Ca²⁺ leak channel and their property as leak channel was addressed upon overexpression. Calcium homeostasis modulator 1 (CALHM1) increased Ca²⁺ efflux from the ER and reduced activity of SERCA (Gallego-Sandín et al., 2011), but the restricted and low expression of CALHM1 in tissues of the brain, kidney, bladder and immune cells render it an unlikely candidate as ubiquitous Ca²⁺ leak channel (https://www.proteinatlas.org). The proposed reverse Ca²⁺ flux through the SERCA pump of myocytes could represent yet another source of Ca²⁺ efflux from the ER (Shannon et al., 2000). Interestingly, a short splice variant of SERCA1 (S1T) found in different human tissues reduces ER Ca²⁺ loading via increased passive Ca²⁺ efflux from the ER and reduces activity of SERCA1 and SERCA2. S1T is induced during ER stress, homodimerizes and elevates ER Ca²⁺ depletion for induction of apoptosis, thus rendering S1T a specialized Ca²⁺ leak channel under stress conditions (Chami et al., 2001, 2008). However, the ubiquitously expressed, ER resident Sec61 complex with its pore forming subunit represents an ideal candidate as omnipresent passive Ca²⁺ leak channel. A genome-wide RNAi screen in Drosophila S2 cells identified Sec61α (but none of the aforementioned candidates) as component reducing Ca²⁺ release-activated Ca²⁺ channel activity (Zhang et al., 2006). Though, with such a highly abundant Ca²⁺ leak channel it is imperative to prevent excessive ER Ca²⁻-efflux and disturbance of the Ca²⁺-gradient across the ER membrane. Therefore, Sec61 channel gating has to be tightly controlled as described below (Figure 5).

Single-channel recordings from planar lipid bilayers characterized the Sec61 complex as a highly dynamic aqueous channel with a main calcium conductance of 165 ± 10 pS and a subconductance state of 733 ± 16 pS allowing a rough estimation about the opening diameter of the pore from 5 to 7 Å for the main conductance and 12–14 Å for the subconductance state. The Sec61 complex is transiently opened by signal peptides within precursor polypeptides and is permeable to Ca²⁺ at the end of protein translocation (Simon et al., 1989; Wirth et al., 2003; Erdmann et al., 2011; Lang et al., 2011). The same experimental strategy showed that the Sec61 channel closes either spontaneously or as induced by binding of BiP or Ca²⁺-calmodulin (Erdmann et al., 2011; Schäuble et al., 2012). The fact that BiP is involved in closing the Sec61 channel was confirmed at the cellular level by combination of siRNA-mediated gene silencing or pharmacological manipulation and live cell Ca²⁺ imaging (Schäuble et al., 2012). In addition, cytosolic Ca²⁺-calmodulin was shown under similar conditions to contribute to Sec61 channel closing via an unrelated mechanism once Ca²⁺ has started to leak from the ER (Erdmann et al., 2011). During the last 5 years, additional siRNA-mediated gene silencing and live cell Ca²⁺ imaging experiments characterized the pair of ERj 3 and 6 as co-chaperones of BiP as well as Ca²⁺-Sec62 as a co-factor of calmodulin in Sec61 channel closure (Linxweiler et al., 2013; Schorr et al., 2015). Furthermore, the binding sites of BiP, Ca²⁺-calmodulin, and Ca²⁺-Sec62 were identified as the abovementioned di-tyrosine motif–containing mini-helix within ER lumenal loop 7 of the Sec61 α-subunit and an IQ motif in the cytosolic amino-terminus of the same subunit, respectively (Figure 5). Furthermore, the respective affinities of these interactions were determined by surface plasmon resonance spectroscopy and found to be physiologically relevant (Figure 6).

The following scenario for gating of the Sec61 channel has emerged from these studies (reviewed by Zimmermann et al., 2011; Dudek et al., 2015; Pfeffer et al., 2016; Zimmermann, 2016; Figure 5). As described above, binding of a precursor polypeptide to the closed Sec61 complex triggers channel opening, either on its own or facilitated by binding of the allosteric modulator of the Sec61 channel, BiP (Schäuble et al., 2012; Figure 5). Here, Sec63 acts as a BiP co-chaperone (Lang et al., 2012). After completion of protein translocation, i.e., in the absence of any bound precursor polypeptide, the channel closes on its own, or BiP facilitates efficient gating of the Sec61 channel to the closed state (Schäuble et al., 2012). At this stage, ERj3 and ERj6 are BiP co-chaperones, possibly acting in the form of a heterodimeric complex (Schorr et al., 2015). The idea is that binding of BiP to loop 7 of Sec61α provides energy for shifting the dynamic equilibrium of the Sec61 channel to the closed state. The idea that such a mechanism may indeed be at work came from single-channel recordings where Fab fragments directed against loop 7 could substitute for BiP in channel closing (Schorr et al., 2015). In case of inefficient channel closure in intact cells, Ca²⁺ starts to leak from the ER into the cytosol and binds calmodulin, and Ca²⁺-calmodulin is recruited to the IQ motif in the Sec61 α-subunit (Erdmann et al., 2011; Figures 5, 6). Once again, the involved binding energy may favor channel closure. Binding of Ca²⁺-calmodulin is supported by Sec62, which may have bound Ca²⁺ because of a predicted EF hand within its cytosolic carboxy-terminal end (Linxweiler et al., 2013). Next, the Sec61 channel is closed, and Ca²⁺ leakage subsides. SERCA pumps Ca²⁺ back into the ER, calmodulin and Sec62 return to the Ca²⁺-free forms, and the next protein translocation cycle can be initiated. The crucial open question is if or when the Ca²⁺ permeability of the open Sec61 channel and its elaborate control mechanisms play a physiological role.

As previously outlined (Linxweiler et al., 2017), “an additional function beyond ER protein import and Ca²⁺ homeostasis was recently found for the Sec62 protein and represents yet another example of pathway overlaps (Fumagalli et al., 2016). Sec62 also plays a crucial role in the recovery of eukaryotic cells from conditions of ER stress. In the course of UPR, the level of several ER lumenal chaperones such as BiP is markedly increased (Ma and Hendershot, 2001; Zhang and Kaufman, 2004). If the cell can cope with ER stress conditions, the expanded ER as well as the high amount of ER lumenal chaperones have to be returned to a physiological level. Therefore, small vesicles derived from the ER membrane fuse with phagophores to build autophagosomes (ER-autophagy) (Figure 6). For this purpose, Sec62 bears a LIR motif at its carboxy-terminus that functions as a receptor for phagophore-bound LC3. Thus, Sec62 plays an important, Sec61- and Sec63-independent role during recovery from ER stress.” A similar mechanism may be involved in ER-phagy when mis-folded polypeptides overwhelm the ERAD machinery and whole ER sections have to be sacrificed to protect the cell. We suggest that phosphorylation of the negative patch in the carboxy-terminus of Sec63 and/or Ca²⁺ binding to the EF hand in the carboxy-terminus of Sec62 may trigger dissociation of Sec62 from its interaction partners (Ampofo et al., 2013; Linxweiler et al., 2013).

Novel Concept for Physiologic Roles of the Human Sec61 Channel in Cellular Calcium Homeostasis and Energy Metabolism

As stated above, the Ca²⁺ permeability of the open Sec61 channel may be involved in the intrinsic pathway to apoptosis, i.e., when cells have to be sacrificed to protect a multicellular organism from terminal protein aggregation problems. We suggest that under conditions of severe and prolonged protein mis-folding and aggregation even after UPR induction, BiP is terminally sequestered by mis-folded and aggregating polypeptides. As described, this sequestration will eventually lead to continuous Ca²⁺ leakage from the ER via open Sec61 channels (Figure 2). In the long run, the effect may contribute to increased cytosolic Ca²⁺ levels, which are typically involved in induction of apoptosis. We expect that such a scenario may be particularly relevant for secretory cells, such as the β cells of the pancreas or plasma cells of the immune system. Therefore, these two cell types are particularly sensitive to mutations in the SEC61A1 gene (see below).

To fulfill its central role in protein biogenesis, the ER of all nucleated human cells contains the ATP dependent chaperone BiP in millimolar concentration and, thus, depends on a constant supply of ATP. So far, only for the plant Arabidopsis thaliana an ER-resident membrane ATP carrier has been described (Leroch et al., 2008). Thus, the question remains of how ATP gets into the human ER. Recent work has established a set of hallmarks for this nucleotide transport (Vishnu et al., 2013). There appears to be a regulatory circuit for maintenance of ATP supply of the human ER that involves ER-lumenal and cytosolic Ca²⁺, the elusive ADP/ATP carrier, and cytosolic AMP–activated protein kinase (AMPK) (Figure 2). Decreasing ATP levels in the ER leads to decreasing ER Ca²⁺- and increasing cytosolic Ca²⁺ levels, where the former activates the ER membrane–resident ADP/ATP carrier and the latter stimulates ADP phosphorylation in cytosol and mitochondria. Based on our observations on the Ca²⁺ permeability of the open Sec61 channel and its limitation by BiP, we propose that the above-described regulatory circuit for maintenance of ATP supply of the human ER also involves the Sec61 channel in the ER membrane and the ER lumenal BiP. According to this novel concept, decreased ATP levels in the ER should cause lower BiP activity, which in turn causes ER Ca²⁺ leakage via the Sec61 channel, in analogy to the situation where BiP is sequestered by mis-folded polypeptides. Next, decreasing ER lumenal Ca²⁺ activates the ER membrane–resident ADP/ATP carrier, and increasing cytosolic Ca²⁺ stimulates ADP phosphorylation in cytosol and mitochondria. Subsequently, ATP levels in the ER recover, BiP binds to the Sec61 channel and stops Ca²⁺ from leaking into the cytosol. This scenario may also serve as a framework for envisioning how breakdown of energy metabolism can cause apoptosis, e.g., when plasma cells are at the end of their lifespan. In this case, accumulation of mis-folded immunoglobulin polypeptide chains may further aggravate the situation (Kourtis and Tavernarakis, 2011).

Sec61-Channelopathies and Therapeutic Strategies

“In light of this elaborate system of Sec61 channel gating, it did not come as a surprise that various diseases were linked to components of the protein translocation machinery (Zimmermann, 2016).” The term Sec61-channelopathies was coined for the family of inherited or tumor-related diseases that either directly affect Sec61 subunits or are linked to components involved in Sec61 channel gating (Haßdenteufel et al., 2014; Linxweiler et al., 2017; Table 1; Figures 5, 9). Mutations in the gene coding for the Sec61 α-subunit can cause diabetes in the mouse (Lloyd et al., 2010), and common variable immune deficiency (CVID) and tubulo-interstitial kidney disease with anemia in humans (Bolar et al., 2016; Schubert et al., 2017). Loss-of-function mutations in genes coding for Sec63 and ERj6, respectively, were linked to autosomal dominant polycystic liver disease and diabetes in both humans and mice (Davila et al., 2004; Ladiges et al., 2005; Fedeles et al., 2011; Synofzik et al., 2014). Furthermore, polycystic liver disease can be caused by heterozygous mutation of the SEC61B gene (Besse et al., 2017), and proteolytic inactivation of BiP by the bacterial subtilase cytotoxin SubAB causes the devastating hemolytic uremic syndrome (Paton et al., 2006). Overproduction of components of the protein translocation machinery is associated with cancers of prostate, lung, head, and neck (Sec62) and with glioblastoma (Sec61γ) (Lu et al., 2009; Greiner et al., 2011; Linxweiler et al., 2012, 2013; Bochen et al., 2017). In addition, several diseases have been linked to subunits of OST (reviewed by Mohorko et al., 2011) and Sil1 (Senderek et al., 2005; Zhao et al., 2005; Roos et al., 2014), respectively, and appear to affect N-glycosylation of newly synthesized polypeptides and protein folding, respectively, rather than Sec61 channel gating (Table 1). As described before (Zimmermann, 2016), “the human diseases associated with mutations in OST and Sil1 are congenital disorders of glycosylation (CDG) Type I and the neurodegenerative Marinesco-Sjögren Syndrome, respectively. We note that CDG can also result from loss-of-function mutations in genes coding for different subunits of TRAP (Losfeld et al., 2014; Pfeffer et al., 2017; Table 1).

FIGURE 9

Figure 9. Position of disease-linked mutations in 3D reconstructions of the Sec61 complex. See text for details.

In the case of diabetes, loss of ERj6 function and homozygous SEC61A1 mutation, respectively, were suggested to be caused by inefficient gating of Sec61 channels to the closed state with sustained ER Ca²⁺ leakage and, eventually, apoptosis of secretory cells, such as pancreatic ß cells (Schäuble et al., 2012; Schorr et al., 2015). The former is in agreement with ERj6 being involved in gating of the Sec61 channel to the closed state. The latter was explained by the observation that the diabetes-linked mutation of the SEC61A1 tyrosine 344 to histidine affects the di-tyrosine motif-containing mini-helix of the Sec61 α-subunit, i.e., the BiP-binding site (Schäuble et al., 2012; Figures 5, 9).” As a consequence, the mutated Sec61 channel cannot be efficiently gated by BiP and thus becomes permeable for Ca²⁺. A similarly permeable Sec61 channel may exist in case of CVID, where a heterozygous mutation of the SEC61A1 gene (resulting in the substitution of valine 85 by aspartate) introduces a polar amino acid side chain into the typically non-polar “pore ring” of the Sec61 channel (Schubert et al., 2017). This view was supported by the observation that the CVID-linked mutation, when introduced into HeLa cells, leads to permeable Sec61 channels, which may have a dominant-negative effect on the cells. Therefore, the lifespan of plasma cells may be shortened in the patients. Alternatively, the disease phenotype may be caused by haploinsufficiency. The functional consequences are less clear in the case of tubulo-interstitial kidney disease, where two mutations in the SEC61A1 gene have been reported (resulting in the substitution of valine 67 by glycine and of threonine 185 by valine), which are located in the “plug” domain and transmembrane helix 5, respectively (Bolar et al., 2016). In all diseases that are related to the ubiquitously expressed SEC61A1 gene, the crucial question is why a particular mutation affects only a single cell type.

In the case of polycystic liver disease, reduction or loss of Sec63 function appears to cause a precursor polypeptide-specific defect in ER protein import, which results in the absence of certain plasma membrane proteins, such as polycystin 1, involved in planar cell polarity (Davila et al., 2004; Fedeles et al., 2011). This association is consistent with the idea that Sec63 is involved in gating of the Sec61 channel to the open state. In addition, the interaction of Sec63 with cytosolic nucleoredoxin may be relevant for the disease phenotype (Müller et al., 2011). Apparently, the loss-of-function mutation of the SEC61B allele also causes a precursor-specific ER protein import defect. Again, the open question is why only a certain cell type, in this case cholangiocytes, is affected by the partial or complete loss of function.

It appears that excessively efficient closing of the Sec61 channel can also lead to disease (Linxweiler et al., 2012, 2013). Amplification and/or over-expression of the SEC62 gene (also termed TLOC1) were linked to various cancers and appear to be associated with poor prognosis. SEC62 over-expression was found to result in elevated migratory potential and increased stress tolerance of the respective tumor cells, i.e., two “hallmarks” of cancer cells with a connection to cellular Ca²⁺ homeostasis. Furthermore, the SEC62 gene has been characterized as a “tumor driver gene” (Hagerstrand et al., 2013). The two cancer hallmarks of SEC62 over-expressing tumor cells can be overcome by siRNA-mediated gene silencing (Linxweiler et al., 2013). Based on our data on the role of Sec62 in Sec61 channel gating, we asked whether the effect of SEC62 silencing on SEC62 over-expressing tumor cells can be phenocopied by drugs. We reasoned that if Ca²⁺-calmodulin secures efficient Sec61 channel closure in cooperation with Ca²⁺-Sec62, calmodulin antagonists should mimick the effect of SEC62 silencing on SEC62 over-expressing tumor cells; indeed, this is what we found. One particular calmodulin antagonist of interest is trifluoperazine, since it has previously been in clinical use for depressive patients. Thus, we are currently addressing in murine tumor models if proliferation of SEC62 over-expressing tumor cells can be inhibited by a combinatorial treatment that includes trifluoperazine and a SERCA inhibitor. We note that SERCA-targeting prodrugs are currently being evaluated in clinical trials (Mahalingam et al., 2016).

Sec61 Channel Inhibitors, an Epilog

In the course of the last 10 years, several small molecule inhibitors of the Sec61 channel have been discovered which, in analogy to mutations of the SEC61A1 gene, affect ER protein import in a precursor-specific or non-selective manner. The first-described and precursor-selective class of such inhibitors were the cyclic heptadepsipeptides, i.e., CAM749 and cotransins (such as CT8) (Besemer et al., 2005; Garrison et al., 2005; MacKinnon et al., 2014). Subsequently, the structurally unrelated compounds apratoxin A and mycolactone were characterized as Sec61 effectors and shown to have selective (mycolactone) or non-selective (apratoxin A) effects on ER protein import by interaction with the channel (Liu et al., 2009; Hall et al., 2014; Baron et al., 2016; McKenna et al., 2016, 2017; Paatero et al., 2016). The model to explain a precursor-specific inhibitory effect suggests that certain signal peptides and transmembrane helices can either bypass or displace the drugs during their initial insertion into the Sec61 channel. Thus, both possibilities may, at least in some way, reiterate the above discussion of “weak” and “strong” signal peptides (see above): the bound small molecules may increase the energy barrier involved in opening of the Sec61 channel for protein translocation and precursors with “strong” signal peptides may overcome the barrier anyhow (Figure 8). Alternatively, selective inhibitors may occupy binding sites within the Sec61 channel, which are irrelevant for some signal peptides. Therefore, the exact mode of action of these compounds is an important open question. Furthermore, it will be interesting to address the questions of whether or not the selectivity of some of the small molecules correlates with the dependence of some precursors on certain auxiliary components in gating of the channel and if and how the inhibitory compounds affect cellular Ca²⁺ homeostasis.

Intriguingly, heptadepsipeptides are considered for the treatment of multiple myeloma, which is very much in line with the observation in CVID patients that physiological levels of functional Sec61 channels are essential for plasma cell viability. Mycolactone appears to be a good candidate to follow that same path.

Concluding Remarks

The mammalian Sec61 complex forms a dynamic and precursor gated channel, which can provide an aqueous path for polypeptides into the ER lumen and is regulated by various allosteric effectors. When the aqueous path is open, it can apparently also provide a channel for efflux of calcium ions from the ER lumen into the cytosol. We suggest that this feature is linked to the regulation of ATP import into the ER and the initiation of the intrinsic pathway to apoptosis, respectively. To us, the most pressing open questions concern (i) the structure of the native Sec61 complex in the ribosome-free state, (ii) the positioning of other transport and processing components within the native translocon, (iii) the rules of engagement of the allosteric effectors of the Sec61 channel plus their molecular mechanisms. The latter will undoubtedly also pave the way for a detailed understanding of the pathomechanisms which are involved in Sec61 channelopathies. Another burning question is the nature of the elusive ATP carrier(s) of the mammalian ER membrane.

Author Contributions

SP and FF contributed 3D reconstructions after CET. PL and VH performed molecular modelings. SL and RZ wrote the first draft of the manuscript, which was contributed to by all authors.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

The authors are grateful to Drs Lars Kästner and Peter Lipp (Cell Biology, Saarland University, Homburg, Germany) for donating 3D reconstructions of cells after live cell fluorescence imaging, to Daniel Wiebelt and Maria Zimmermann for contributing artwork, and to the Deutsche Forschungsgemeinschaft (DFG) for continuous financial support.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fphys.2017.00887/full#supplementary-material

Supplementary Video 1. Artist's view of SRP/SR, BiP and Sec63 mediated transport of presecretory proteins via the Sec61 channel into the ammalian ER. J, J-domain of Sec63 recruits BiP to the Sec61 channel for channel opening and to incoming precursor polypeptides for ratcheting, respectively. Signal peptidase (SPase) cleaves the signal peptide from the incoming precursor polypeptide. See text for details.

References

Alberti, S., Esser, C., and Höhfeld, J. (2003). BAG-1—a nucleotide exchange factor of Hsc70 with multiple cellular functions. Cell Stress Chaperones 8, 225–231.

PubMed Abstract | Google Scholar

Ampofo, E., Welker, S., Jung, M., Müller, L., Greiner, M., Zimmermann, R., et al. (2013). CK2 phosphorylation of human Sec63 regulates its interaction with Sec62. Biochim. Biophys. Acta 1830, 2938–2945. doi: 10.1016/j.bbagen.2012.12.020

PubMed Abstract | CrossRef Full Text | Google Scholar

Ast, T., Cohen, G., and Schuldiner, M. (2013). A network of cytosolic factors targets SRP-independent proteins to the endoplasmic reticulum. Cell 152, 1134–1145. doi: 10.1016/j.cell.2013.02.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Ast, T., Michaelis, S., and Schuldiner, M. (2016). The protease Ste24 clears clogged translocons. Cell 164, 103–114. doi: 10.1016/j.cell.2015.11.053

PubMed Abstract | CrossRef Full Text | Google Scholar

Aviram, N., Ast, T., Costa, E. A., Arakel, E., Chuartzman, S. G., Jan, C. H., et al. (2016). The SND proteins constitute an alternative targeting route to the endoplasmic reticulum. Nature 540, 134–138. doi: 10.1038/nature20169

PubMed Abstract | CrossRef Full Text | Google Scholar

Aviram, N., and Schuldiner, M. (2014). Embracing the void-how much do we really know about targeting and translocation to the endoplasmic reticulum? Curr. Opin. Cell Biol. 29, 8–17. doi: 10.1016/j.ceb.2014.02.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Bagola, K., Mehnert, M., Jarosch, E., and Sommer, T. (2011). Protein dislocation from the ER. Biochim. Biophys. Acta 1808, 925–936. doi: 10.1016/j.bbamem.2010.06.025

PubMed Abstract | CrossRef Full Text | Google Scholar

Bañó-Polo, M., Martínez-Garay, C. A., Grau, B., Martínez-Gil, L., and Mingarro, I. (2017). Membrane insertion and topology of the translocon-associated protein (TRAP) gamma subunit. Biochim. Biophys. Acta 1859, 903–909. doi: 10.1016/j.bbamem.2017.01.027

PubMed Abstract | CrossRef Full Text | Google Scholar

Baron, L., Onerva Paatero, A., Morel, J.-D., Impens, F., Guenin-Mace, L., Saint-Auret, S., et al. (2016). Mycolactone subverts immunity by selectively blocking the Sec61 translocon. J. Exp. Med. 213, 2885–2896. doi: 10.1084/jem.20160662

PubMed Abstract | CrossRef Full Text | Google Scholar

Benedix, J., Lajoie, P., Jaiswal, H., Burgard, C., Greiner, M., Zimmermann, R., et al. (2010). BiP modulates the affinity of its co-chaperone ERj1 to ribosomes. J. Biol. Chem. 285, 36427–36433. doi: 10.1074/jbc.M110.143263

PubMed Abstract | CrossRef Full Text | Google Scholar

Berbey, C., Weiss, N., Legrand, C., and Allard, B. (2009). Transient receptor potential canonical type 1 (TRPC1) operates as a sarcoplasmic reticulum calcium leak channel in skeletal muscle. J. Biol. Chem. 284, 36387–36394. doi: 10.1074/jbc.M109.073221

PubMed Abstract | CrossRef Full Text | Google Scholar

Berridge, M. J. (2002). The endoplasmic reticulum: a multifunctional signalling organelle. Cell Calc. 32, 235–249. doi: 10.1016/S0143416002001823

PubMed Abstract | CrossRef Full Text | Google Scholar

Besemer, J., Harant, H., Wang, S., Oberhauser, B., Marquardt, K., Foster, C. A., et al. (2005). Selective inhibition of cotranslational translocation of vascular cell adhesion molecule 1. Nature 436, 290–293. doi: 10.1038/nature03670

PubMed Abstract | CrossRef Full Text | Google Scholar

Besse, W., Choi, J., Punia, S., Fedeles, S. V., Choi, M., Gallagher, A.-R., et al. (2017). Isolated polycystic liver disease genes define effectors. Of poylcystin-1 function. J. Clin. Invest. 27, 1772–1785. doi: 10.1172/JCI90129

CrossRef Full Text | Google Scholar

Blau, M., Mullapudi, S., Becker, T., Dudek, J., Zimmermann, R., Penczek, P. A., et al. (2005). ERj1p uses a universal ribosomal adaptor site to coordinate the 80S ribosome at the membrane. Nat. Struct. Mol. Biol. 12, 1015–1016. doi: 10.1038/nsmb998

PubMed Abstract | CrossRef Full Text | Google Scholar

Blobel, G., and Dobberstein, B. (1975). Transfer of proteins across membranes: I. Presence of proteolytically processed and unprocessed nascent immunoglobulin light chains on membrane-bound ribosomes of murine myeloma. J. Cell Biol. 67, 835–851.

PubMed Abstract | Google Scholar

Blond-Elguindi, S., Cwirla, S. E., Dower, W. J., Lipshutz, R. J., Sprang, S. R., Sambrook, J. F., et al. (1993). Affinity panning of a library of peptides displayed on bacteriophages reveals the binding specificity of BiP. Cell 75, 717–728. doi: 10.1016/0092-8674(93)90492-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Bochen, F., Adisurya, H., Wemmert, S., Lerner, C., Greiner, M., Zimmermann, R., et al. (2017). Effect of 3q oncogenes SEC62 and SOX2 on lymphatic metastasis and clinical outcome of head and neck squamous cell carcinomas. Oncotarget 8, 4922–4934. doi: 10.18632/oncotarget.13986

PubMed Abstract | CrossRef Full Text | Google Scholar

Bolar, N. A., Golzio, C., Zivna, M., Hyot, G., van Hemelrijk, C., Schepers, D., et al. (2016). Heterozygous loss-of-function SEC61A mutations cause autosomal-dominant tubule-interstitial and glomerulocystic kidney disease with anemia. Am. J. Hum. Gen. 99, 174–187. doi: 10.1016/j.ajhg.2016.05.028

CrossRef Full Text | Google Scholar

Borgese, N., and Fasana, E. (2011). Targeting pathways of C-tail-anchored proteins. Biochim. Biophys. Acta 1808, 937–946. doi: 10.1016/j.bbamem.2010.07.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Braakman, I., and Bulleid, N. J. (2011). Protein folding and modification in the mammalian endoplasmic reticulum. Ann. Rev. Biochem. 80, 71–99. doi: 10.1146/annurev-biochem-062209-093836

PubMed Abstract | CrossRef Full Text | Google Scholar

Bracher, A., and Verghese, J. (2015). The nucleotide exchange factors of Hsp70 molecular chaperones. Front. Mol. Biosci. 2:10. doi: 10.3389/fmolb.2015.00010

PubMed Abstract | CrossRef Full Text | Google Scholar

Brostrom, M. A., and Brostrom, C. O. (2003). Calcium dynamics and endoplasmic reticular function in the regulation of protein synthesis: implications for cell growth and adaptability. Cell Calcium 34, 345–363. doi: 10.1016/S0143-4160(03)00127-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Chami, M., Gozuacik, D., Lagorce, D., Brini, M., Falson, P., Peaucellier, G., et al. (2001). SERCA1 truncated proteins unable to pump calcium reduce the endoplasmic reticulum calcium concentration and induce apoptosis. J. Cell Biol. 153, 1301–1314. doi: 10.1083/jcb.153.6.1301

PubMed Abstract | CrossRef Full Text | Google Scholar

Chami, M., Oules, B., Szabadkai, G., Tacine, R., Rizzuto, R., and Paterlini-Bréchot, P. (2008). Role of SERCA1 truncated isoform in the proapoptotic calcium transfer from ER to mitochondria during ER stress. Mol. Cell. 32, 641–651. doi: 10.1016/j.molcel.2008.11.014

PubMed Abstract | CrossRef Full Text | Google Scholar

Chami, M., Prandini, A., Campanella, M., Pinton, P., Szabadkai, G., Reed, J. C., et al. (2004). Bcl-2 and Bax exert opposing effects on Ca²⁺ signaling, which do not depend on their putative pore-forming region. J. Biol. Chem. 279, 54581–54589. doi: 10.1074/jbc.M409663200

CrossRef Full Text | Google Scholar

Cheetham, M. E., and Caplan, A. J. (1998). Structure, function and evolution of DnaJ: conservation and adaptation of chaperone function. Cell Stress Chaperones 3, 28–36. doi: 10.1379/1466-1268(1998)003<0028:SFAEOD>2.3.CO;2

PubMed Abstract | CrossRef Full Text | Google Scholar

Chen, Q., Denard, B., Lee, C.-E., Han, S., Ye, J. S., and Ye, J. (2016). Inverting the topology of a transmembrane protein by regulating the translocation of the first transmembrane helix. Mol. Cell, 63, 567–578. doi: 10.1016/j.molcel.2016.06.032

PubMed Abstract | CrossRef Full Text | Google Scholar

Cheung, K. H., Mei, L., Mak, D. O. D., Hayashi, I., Iwatsubo, T., Kang, D. E., et al. (2010). Gain-of-function enhancement of IP3-receptor modal gating by familial Alzheimer's disease-linked presenilin mutants in human cells and mouse neurons. Sci. Signal. 3:ra22. doi: 10.1126/scisignal.2000818

PubMed Abstract | CrossRef Full Text | Google Scholar

Cheung, K.-H., Shineman, D., Müller, M., Cárdenas, C., Mei, L., Yang, J., et al. (2008). Mechanism of Ca²⁺ disruption in Alzheimer's disease by presenilin regulation of InsP₃-receptor channel gating. Neuron 58, 871–883. doi: 10.1016/j.neuron.2008.04.015

PubMed Abstract | CrossRef Full Text | Google Scholar

Clapham, D. E. (2007). Calcium Signaling. Cell 131, 1047–1058. doi: 10.1016/j.cell.2007.11.028

PubMed Abstract | CrossRef Full Text | Google Scholar

Conti, B. J., Devaraneni, P. K., Yang, Z., David, L. L., and Skach, W. R. (2015). Cotranslational stabilization of Sec62/63 within the ER Sec61 translocon is controlled by distinct substrate-driven translocation events. Mol. Cell 58, 269–283. doi: 10.1016/j.molcel.2015.02.018

PubMed Abstract | CrossRef Full Text | Google Scholar

Davila, S., Furu, L., Gharavi, A. G., Tian, X., Onoe, T., Qian, Q., et al. (2004). Mutations in SEC63 cause autosomal dominant polycystic liver disease. Nat. Gen. 36, 575–577. doi: 10.1038/ng1357

PubMed Abstract | CrossRef Full Text | Google Scholar

Deshaies, R. J., and Schekman, R. (1987). A yeast mutant defective at an early stage in import of secretory protein precursors into the endoplasmic reticulum. J. Cell Biol. 105, 633–645. doi: 10.1083/jcb.105.2.633

PubMed Abstract | CrossRef Full Text | Google Scholar

Devaraneni, P. K., Conti, B., Matsumara, Y., Yang, Z., Johnson, A. E., and Skach, W. R. (2011). Stepwise insertion and inversion of a type II signal anchor sequence in the ribosome-Sec61 translocon complex. Cell 146, 134–147. doi: 10.1016/j.cell.2011.06.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Dudek, J., Benedix, J., Cappel, S., Greiner, M., Jalal, C., Müller, L., et al. (2009). Functions and pathologies of BiP and its interaction partners. Cell. Mol. Life Sci. 65, 1556–1569. doi: 10.1007/s00018-009-8745-y

CrossRef Full Text | Google Scholar

Dudek, J., Greiner, M., Müller, A., Hendershot, L. M., Kopsch, K., Nastainczyk, W., et al. (2005). ERj1p plays a basic role in protein biogenesis at the endoplasmic reticulum. Nat. Struct. Mol. Biol. 12, 1008–1014. doi: 10.1038/nsmb1007

CrossRef Full Text | Google Scholar

Dudek, J., Pfeffer, S., Lee, P.-H., Jung, M., Cavalié, A., Helms, V., et al. (2015). Protein transport into the human endoplasmic reticulum. J. Mol. Biol. 427, 1159–1175. doi: 10.1016/j.jmb.2014.06.011

PubMed Abstract | CrossRef Full Text | Google Scholar

Ellgaard, L., and Helenius, A. (2003). Quality control in the endoplasmic reticulum. Nat. Rev. Mol. Cell Biol. 4, 181–191. doi: 10.1038/nrm1052

PubMed Abstract | CrossRef Full Text | Google Scholar

Erdmann, F., Schäuble, N., Lang, S., Jung, M., Honigmann, A., Ahmad, M., et al. (2011). Interaction of calmodulin with Sec61α limits Ca²⁺ leakage from the endoplasmic reticulum. EMBO J. 30, 17–31. doi: 10.1038/emboj.2010.284

PubMed Abstract | CrossRef Full Text | Google Scholar

Fedeles, S. V., Tian, X., Gallagher, A.-R., Mitobe, M., Nishio, S., et al. (2011). A genetic interaction network of five genes for human polycystic kidney and liver disease defines polycystin-1 as the central determinant of cyst formation. Nat. Gen. 43, 639–647. doi: 10.1038/ng.860

CrossRef Full Text | Google Scholar

Flynn, G. C., Pohl, J., Flocco, M. T., and Rothman, J. E. (1991). Peptide-binding specificity of the molecular chaperone BiP. Nature 353, 726–730. doi: 10.1038/353726a0

PubMed Abstract | CrossRef Full Text | Google Scholar

Fons, R. D., Bogert, B. A., and Hegde, R. S. (2003). Substrate-specific function of the translocon-associated protein complex during translocation across the ER membrane. J. Cell Biol. 160, 529–539. doi: 10.1083/jcb.200210095

PubMed Abstract | CrossRef Full Text | Google Scholar

Friedman, J. R., and Voeltz, G. K. (2011). The ER in 3D: a multifunctional dynamic membrane network. Trends Cell Biol. 21, 709–717. doi: 10.1016/j.tcb.2011.07.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Fumagalli, F., Noack, J., Bergmann, T., Cebollero, E., Pisoni, G. B., Fasana, E., et al. (2016). Translocon component Sec62 acts in endoplasmic reticulum turnover during stress recovery. Nat. Cell Biol. 18, 1173–1184. doi: 10.1038/ncb3423

PubMed Abstract | CrossRef Full Text | Google Scholar

Gallego-Sandín, S., Alonso, M. T., and García-Sancho, J. (2011). Calcium homoeostasis modulator 1 (CALHM1) reduces the calcium content of the endoplasmic reticulum (ER) and triggers ER stress. Biochem. J. 437, 469–475. doi: 10.1042/BJ20110479

PubMed Abstract | CrossRef Full Text | Google Scholar

Gamerdinger, M., Hanebuth, M. A., Frickey, T., and Deuerling, E. (2015). The principle of antagonism ensures protein targeting specificity at the endoplasmic reticulum. Science 348, 201–207. doi: 10.1126/science.aaa5335

PubMed Abstract | CrossRef Full Text | Google Scholar

Garrison, J. L., Kunkel, E. J., Hegde, R. S., and Taunton, J. (2005). A substrate-specific inhibitor of protein translocation into the endoplasmic reticulum. Nature 436, 285–289. doi: 10.1038/nature03821

PubMed Abstract | CrossRef Full Text | Google Scholar

Gilmore, R., Blobel, G., and Walter, P. (1982). Protein translocation across the endoplasmic reticulum. I. Detection in the microsomal membrane of a receptor for the signal recognition particle. J. Cell Biol. 95, 463–469. doi: 10.1083/jcb.95.2.463

PubMed Abstract | CrossRef Full Text | Google Scholar

Gogala, M., Becker, T., Beatrix, B., Armache, J.-P., Barrio-Garcia, C., Berninghausen, O., et al. (2014). Structures of the Sec61 complex engaged in nascent peptide translocation or membrane insertion. Nature 506, 107–110. doi: 10.1038/nature12950

CrossRef Full Text | Google Scholar

Görlich, D., and Rapoport, T. A. (1993). Protein translocation into proteoliposomes reconstituted from purified components of the endoplasmic reticulum membrane. Cell 75, 615–630. doi: 10.1016/0092-8674(93)90483-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Görlich, D., Prehn, S., Hartmann, E., Kalies, K.-U., and Rapoport, T. A. (1992). A mammalian homolog of SEC61p and SECYp is associated with ribosomes and nascent polypeptides during translocation. Cell 71, 489–503. doi: 10.1016/0092-8674(92)90517-G

PubMed Abstract | CrossRef Full Text | Google Scholar

Greiner, M., Kreutzer, B., Lang, S., Jung, V., Cavalié, A., Unteregger, G., et al. (2011). Sec62 protein level is crucial for ER-stress tolerance of prostate cancer. Prostate 71, 1074–1083. doi: 10.1002/pros.21324

PubMed Abstract | CrossRef Full Text | Google Scholar

Gumbart, J., Trabuco, L. G., Schreiner, E., Villa, E., and Schulten, K. (2009). Regulation of the protein-conducting channel by a bound ribosome. Structure 17, 1453–1464. doi: 10.1016/j.str.2009.09.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Haas, I. G., and Wabl, M. (1983). Immunoglobulin heavy chain binding protein. Nature 306, 387–389. doi: 10.1038/306387a0

PubMed Abstract | CrossRef Full Text | Google Scholar

Hagerstrand, D., Tong, A., Schumacher, S. E., Ilic, N., Shen, R. R., Cheung, H. W., et al. (2013). Systematic interrogation of 3q26 identifies TLOC1 and SKIL as cancer drivers. Cancer Discov. 3, 1045–1057. doi: 10.1158/2159-8290.CD-12-0592

PubMed Abstract | CrossRef Full Text | Google Scholar

Halic, M., Becker, T., Pool, M. R., Spahn, C. M. T., Grassucci, R. A., Frank, J., et al. (2004). Structure of the signal recognition particle interacting with the elongation-arrested ribosome. Nature 427, 808–814. doi: 10.1038/nature02342

PubMed Abstract | CrossRef Full Text | Google Scholar

Halic, M., Blau, M., Becker, T., Mielke, T., Pool, M. R., Wild, K., et al. (2006). Following the signal sequence from ribosomal tunnel exit to signal recognition particle. Nature 444, 507–511. doi: 10.1038/nature05326

PubMed Abstract | CrossRef Full Text | Google Scholar

Hall, B. S., Hill, K., McKenna, M., Ogbechi, J., High, S., Willis, A. E., et al. (2014). The pathogenic mechanism of the Mycobacterium ulcerans virulence factor, mycolactone, depends on blockade of protein translocation into the ER. PLOS Pathog. 10:e1004061. doi: 10.1371/journal.ppat.1004061

PubMed Abstract | CrossRef Full Text | Google Scholar

Hartmann, E., Görlich, D., Kostka, S., Otto, A., Kraft, R., Knespel, S., et al. (1993). A tetratmeric complex of membrane proteins in the endoplasmic reticulum. Eur. J. Biochem. 214, 375–381. doi: 10.1111/j.1432-1033.1993.tb17933.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Haßdenteufel, S., Klein, M.-C., Melnyk, A., and Zimmermann, R. (2014). Protein transport into the human ER and related diseases: Sec61-channelopathies. Biochem. Cell Biol. 92, 499–509. doi: 10.1139/bcb-2014-0043

PubMed Abstract | CrossRef Full Text | Google Scholar

Haßdenteufel, S., Schäuble, N., Cassella, P., Leznicki, P., Müller, A., High, S., et al. (2011). Calcium-calmodulin inhibits tail-anchored protein insertion into the mammalian endoplasmic reticulum membrane. FEBS Lett. 585, 3485–3490. doi: 10.1016/j.febslet.2011.10.008

CrossRef Full Text | Google Scholar

Haßdenteufel, S., Sicking, M., Schorr, S., Aviram, N., Fecher-Trost, C., Schuldiner, M., et al. (2017). hSnd2 protein represents an alternative targeting factor to the endoplasmic reticulum in human cells. FEBS Lett. 591, 3211–3224. doi: 10.1002/1873-3468.12831

PubMed Abstract | CrossRef Full Text

Hegde, R. S., Voigt, S., Rapoport, T. A., and Lingappa, V. R. (1998). TRAM regulates the exposure of nascent secretory proteins to the cytosol during translocation into the endoplasmic reticulum. Cell 92, 621–631. doi: 10.1016/S0092-8674(00)81130-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Hegde, R., and Bernstein, H. (2006). The surprising complexity of signal peptides. Trends Biochem. Sci. 31, 563–571. doi: 10.1016/j.tibs.2006.08.004

CrossRef Full Text | Google Scholar

Hein, M. Y., Hubner, N. C., Poser, I., Cox, J., Nagaraj, N., Toyoda, Y., et al. (2015). A human interactome in three quantitative dimensions organized by stoichiometries and abundances. Cell 163, 712–723. doi: 10.1016/j.cell.2015.09.053

PubMed Abstract | CrossRef Full Text | Google Scholar

Hennessy, F., Nicoll, W. S., Zimmermann, R., Cheetham, M. E., and Blatch, G. L. (2005). Not all J domains are created equal: implications for the specificity of Hsp40-Hsp70 interactions. Protein Sci. 14, 1697–1709. doi: 10.1110/ps.051406805

PubMed Abstract | CrossRef Full Text | Google Scholar

Jadhav, B., McKenna, M., Johnson, N., High, S., Sinning, I., and Pool, M. (2015). Mammalian SRP receptor switches the Sec61 translocase from Sec62 to SRP-dependent translocation. Nat. Commun. 6:10133. doi: 10.1038/ncomms10133

PubMed Abstract | CrossRef Full Text | Google Scholar

Johnson, N., Haßdenteufel, S., Theis, M., Paton, A. W., Paton, J. C., Zimmermann, R., et al. (2013). The signal sequence influences posttranslational ER translocation at distinct stages. PLoS ONE 8:e75394. doi: 10.1371/journal.pone.0075394

CrossRef Full Text | Google Scholar

Johnson, N., Vilardi, F., Lang, S., Leznicki, P., Zimmermann, R., and High, S. (2012). TRC-40 can deliver short secretory proteins to the Sec61 translocon. J. Cell Sci. 125, 3612–3620. doi: 10.1242/jcs.102608

CrossRef Full Text | Google Scholar

Junne, T., and Spiess, M. (2017). Integration of transmembrane domains is regulated by their downstream sequences. J. Cell Sci. 130, 372–381. doi: 10.1242/jcs.194472

PubMed Abstract | CrossRef Full Text | Google Scholar

Kanda, S., Yanagitani, K., Yokota, Y., Esaki, Y., and Kohno, K. (2016). Autonomous translational pausing is required for Xbp1u Mrna recruitment to the ER via the SRP pathway. Proc. Natl. Acad. Sci. U.S.A 113, E5886–E5895. doi: 10.1073/pnas.1604435113

PubMed Abstract | CrossRef Full Text | Google Scholar

Kang, S. W., Rane, N. S., Kim, S. J., Garrison, J. L., Taunton, J., and Hegde, R. S. (2006). Substrate-specific translocational attenuation during ER stress defines a pre-emptive quality control pathway. Cell 127, 999–1013. doi: 10.1016/j.cell.2006.10.032

PubMed Abstract | CrossRef Full Text | Google Scholar

Khaminets, A., Heinrich, T., Mari, M., Grumati, P., Huebner, A. K., Akutsu, M., et al. (2015). Regulation of endoplasmic reticulum turnover by selective autophagy. Nature 522, 354–358. doi: 10.1038/nature14498

PubMed Abstract | CrossRef Full Text | Google Scholar

Kourtis, N., and Tavernarakis, N. (2011). Cellular stress response pathways and ageing: intircate molecular relationships. EMBO J. 30, 2520–2531. doi: 10.1038/emboj.2011.162

PubMed Abstract | CrossRef Full Text | Google Scholar

Kutay, U., Ahnert-Hilger, G., Hartmann, E., Wiedenmann, B., and Rapoport, T. A. (1995). Transport route for synaptobrevin via a novel pathway of insertion into the endoplasmic reticulum membrane. EMBO J. 14, 217–223.

PubMed Abstract | Google Scholar

Ladiges, W. C., Knoblaugh, S. E., Morton, J. F., Korth, M. J., Sopher, B. L., Baskin, C. R., et al. (2005). Pancreatic beta-cell failure and diabetes in mice with a deletion mutation of the endoplasmic reticulum molecular chaperone gene P58IPK. Diabetes 54, 1074–1081. doi: 10.2337/diabetes.54.4.1074

PubMed Abstract | CrossRef Full Text | Google Scholar

Lakkaraju, A. K., Thankappan, R., Mary, C., Garrison, J. L., Taunton, J., and Strub, K. (2012). Efficient secretion of small proteins in mammalian cells relies on Sec62-dependent posttranslational translocation. Mol. Biol. Cell 23, 2712–2722. doi: 10.1091/mbc.E12-03-0228

PubMed Abstract | CrossRef Full Text | Google Scholar

Lang, S., Benedix, J., Fedeles, S. V., Schorr, S., Schirra, C., Schäuble, N., et al. (2012). Different effects of Sec61α-, Sec62 and Sec63-depletion on transport of polypeptides into the endoplasmic reticulum of mammalian cells. J. Cell Sci. 125, 1958–1969. doi: 10.1242/jcs.096727

PubMed Abstract | CrossRef Full Text | Google Scholar

Lang, S., Erdmann, F., Jung, M., Wagner, R., Cavalié, A., and Zimmermann, R. (2011). Sec61 complexes form ubiquitous ER Ca²⁺ leak channels. Channels 5, 228–235. doi: 10.4161/chan.5.3.15314

PubMed Abstract | CrossRef Full Text | Google Scholar

Leroch, M., Neuhaus, H. E., Kirchberger, S., Zimmermann, S., Melzer, M., Gerhold, J., et al. (2008). Identification of a novel adenine nucleotide transporter in the endoplasmic reticulum of Arabidopsis. Plant Cell 20, 438–451. doi: 10.1105/tpc.107.057554

PubMed Abstract | CrossRef Full Text | Google Scholar

Leznicki, P., and High, S. (2012). SGTA antagonizes BAG6-mediated protein triage. Proc. Natl. Acad. Sci. U.S.A. 109, 19214–19219. doi: 10.1073/pnas.1209997109

PubMed Abstract | CrossRef Full Text | Google Scholar

Leznicki, P., Clancy, A., Schwappach, B., and High, S. (2010). Bat3 promotes the membrane integration of tail-anchored proteins. J. Cell Sci. 123, 2170–2178. doi: 10.1242/jcs.066738

PubMed Abstract | CrossRef Full Text | Google Scholar

Linxweiler, M., Linxweiler, J., Barth, M., Benedix, J., Jung, V., Kim, Y.-J., et al. (2012). Sec62 bridges the gap from 3q amplification to molecular cell biology in Non-Small Cell Lung Cancer. Am. J. Pathol. 180, 473–483. doi: 10.1016/j.ajpath.2011.10.039

PubMed Abstract | CrossRef Full Text | Google Scholar

Linxweiler, M., Schick, B., and Zimmermann, R. (2017). Lets talk about Secs: Sec61, Sec62, Sec63 in signal transduction, oncology and personalized medicine. Signal Trans. Targ. Ther. 2:e17002. doi: 10.1038/sigtrans.2017.2

CrossRef Full Text | Google Scholar

Linxweiler, M., Schorr, S., Jung, M., Schäuble, N., Linxweiler, J., Langer, F., et al. (2013). Targeting cell migration and the ER stress response with calmodulin antagonists: a clinically tested small molecule phenocopy of SEC62 gene silencing in human tumor cells. BMC Cancer 13:574. doi: 10.1186/1471-2407-13-574

CrossRef Full Text | Google Scholar

Liu, Y., Law, B. K., and Luesch, H. (2009). Apratoxin a reversibly inhibits the secretory pathway by preventing cotranslational translocation. Mol. Pharm. 76, 91–104. doi: 10.1124/mol.109.056085

PubMed Abstract | CrossRef Full Text | Google Scholar

Lloyd, D. J., Wheeler, M. C., and Gekakis, N. (2010). A point mutation inSec61α leads to diabetes and hepatosteatosis in mice. Diabetes 59, 460–470. doi: 10.2337/db08-1362

PubMed Abstract | CrossRef Full Text | Google Scholar

Lomax, R. B., Camello, C., Van Coppenolle, F., Petersen, O. H., and Tepikin, A. V. (2002). Basal and physiological Ca²⁺ leak from the endoplasmic reticulum of pancreatic acinar cells. Second messenger-activated channels and translocons. J. Biol. Chem. 277, 26479–26485 doi: 10.1074/jbc.M201845200

CrossRef Full Text | Google Scholar

Losfeld, M. E., Ng, B. G., Kircher, M., Buckingham, K. J., Turner, E. H., Eroshkin, A., et al. (2014). A new congential disorder of glycosylation caused by a mutation in S.R4, the signal sequence receptor 4 protein of the TRAP complex. Hum. Mol. Gen. 23, 1602–1605. doi: 10.1093/hmg/ddt550

PubMed Abstract | CrossRef Full Text | Google Scholar

Lu, Z., Zhou, L., Killela, P., Rasheed, A. B., Di, C., Poe, W. E., et al. (2009). Glioblastoma proto-oncogene SEC61γ is required for tumor cell survival and response to endoplasmic reticulum stress. Cancer Res. 69, 9105–9111. doi: 10.1158/0008-5472.CAN-09-2775

PubMed Abstract | CrossRef Full Text | Google Scholar

Ma, Y., and Hendershot, L. M. (2001). The unfolding tale of the unfolded protein response. Cell 107, 827–830. doi: 10.1016/S0092-8674(01)00623-7

PubMed Abstract | CrossRef Full Text | Google Scholar

MacKinnon, A. L., Paavilainen, V. O., Sharma, A., Hegde, R. S., and Taunton, J. (2014). An allosteric Sec61 inhibitor traps nascent transmembrane helices at the lateral gate. ELife 3:e01483. doi: 10.7554/eLife.01483

PubMed Abstract | CrossRef Full Text | Google Scholar

Mahalingam, D., Wilding, G., Denmeade, S., Sarantopoulas, J., Cosgrove, J., Cetnar, J., et al. (2016). Mipsagargin, a novel thapsigargin-based PSMA-activated prodrug: results from a first-in-man phase I clinical trial in patients with refractory, advanced or metastatic solid tumors. Br. J. Cancer 114, 986–994. doi: 10.1038/bjc.2016.72

CrossRef Full Text | Google Scholar

Mahamid, J., Pfeffer, S., Schaffer, M., Villa, E., Danev, R., Kuhn Cuellar, L., et al. (2016). Visualizing the molecular sociology at the HeLa cell nuclear periphery. Science 351, 969–972. doi: 10.1126/science.aad8857

PubMed Abstract | CrossRef Full Text | Google Scholar

Mariappan, M., Li, X., Stefanovic, S., Sharma, A., Mateja, A., Keenan, R. J., et al. (2010). A ribosome-associating factor chaperones tail-anchored membrane proteins. Nature 466, 1120–1124. doi: 10.1038/nature09296

PubMed Abstract | CrossRef Full Text | Google Scholar

McKenna, M., Simmonds, R. E., and High, S. (2016). Mechanistic insights into the inhibition of Sec61-dependent co- and post-translational translocation by mycolactone. J. Cell Sci. 129, 1404–1415. doi: 10.1242/jcs.182352

PubMed Abstract | CrossRef Full Text | Google Scholar

McKenna, M., Simmonds, R. E., and High, S. (2017). Mycolactone reveals the substrate-driven complexity of Sec61-dependent transmembrane protein biogenesis. J. Cell Sci. 130, 1307–1320. doi: 10.1242/jcs.198655

PubMed Abstract | CrossRef Full Text | Google Scholar

Melnyk, A., Rieger, H., and Zimmermann, R. (2014). Co-chaperones of the mammalian endoplasmic reticulum. Subcell Biochem. 78, 179–200. doi: 10.1007/978-3-319-11731-7_9

PubMed Abstract | CrossRef Full Text | Google Scholar

Meyer, D. I., and Dobberstein, B. (1980). A membrane component essential for vectorial translocation of nascent proteins across the endoplasmic reticulum: requirements for its extraction and reassociation with the membrane. J. Cell Biol. 8, 498–502. doi: 10.1083/jcb.87.2.498

CrossRef Full Text | Google Scholar

Miller, J. D., Tajima, S., Lauffer, L., and Walter, P. (1995). The ß subunit of the signal recognition particle receptor is a transmembrane GTPase that anchors the α subunit, a peripheral membrane GTPase, to the endoplasmis reticulum membrane. J. Cell Biol. 128, 273–282. doi: 10.1083/jcb.128.3.273

CrossRef Full Text | Google Scholar

Möeller, I., Jung, M., Beatrix, B., Levy, R., Kreibich, G., Zimmermann, R., et al. (1998). A general mechanism for regulation of access to the translocon: competition for a membrane attachment site on ribosomes. Proc. Natl. Acad. Sci. U.S.A. 95, 13425–13430. doi: 10.1073/pnas.95.23.13425

CrossRef Full Text | Google Scholar

Mohorko, E., Glockshuber, R., and Aebi, M. (2011). OST: the central enzyme of N-linked protein glycosylation. J. Inherit. Metab. Dis. 34, 869–878. doi: 10.1007/s10545-011-9337-1

CrossRef Full Text | Google Scholar

Müller, L., Diaz de Escauriaza, M., Lajoie, P., Theis, M., Jung, M., Müller, A., et al. (2010). Evolutionary gain of function of the ER membrane protein Sec62 from yeast to humans. Mol. Biol. Cell 21, 691–703. doi: 10.1091/mbc.E09-08-0730

PubMed Abstract | CrossRef Full Text | Google Scholar

Müller, L., Funato, Y., Miki, H., and Zimmermann, R. (2011). An interaction between human Sec63 with nucleoredoxin may provide the missing link between the SEC63 gene and polycystic liver disease. FEBS Lett. 585, 596–600. doi: 10.1016/j.febslet.2011.01.024

PubMed Abstract | CrossRef Full Text | Google Scholar

Nickel, W., and Rabouille, C. (2009). Mechanisms of regulated unconventional secretion. Nat. Rev. Mol. Cell Biol. 10, 148–155. doi: 10.1038/nrm2617

PubMed Abstract | CrossRef Full Text | Google Scholar

Nixon-Abell, J., Obara, C. J., Weigel, A. V., Li, D., Legant, W. R., Xu, C. S., et al. (2016). Increased spatiotemporal resolution reveals highly dynamic dense tubular matrices in the peripheral ER. Science 354, 433–445. doi: 10.1126/science.aaf3928

PubMed Abstract | CrossRef Full Text | Google Scholar

Novick, P., Field, C., and Schekman, R. (1980). Identification of 23 complementation groups required for post-translational events in the yeast secretory pathway. Cell 21, 205–215. doi: 10.1016/0092-8674(80)90128-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Otero, J. H., Lizák, B., and Hendershot, L. M. (2010). Life and death of a BiP substrate. Semin. Cell Dev. Biol. 21, 472–478. doi: 10.1016/j.semcdb.2009.12.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Paatero, A. O., Kellosalo, J., Dunyak, B. M., Almaliti, J., Gestwicki, J. E., Gerwick, W. H., et al. (2016). Apratoxin kills cells by direct blockade of the Sec61 protein translocation channel. Cell Chem. Biol. 23, 561–566. doi: 10.1016/j.chembiol.2016.04.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Palade, G. (1975). Intracellular aspects of the process of protein synthesis. Science 189, 347–358. doi: 10.1126/science.1096303

CrossRef Full Text | Google Scholar

Park, E., Menetret, J. F., Gumbart, J. C., Ludtke, S. J., Li, W., Whynot, A., et al. (2014). Structure of the SecY channel during initiation of protein translocation. Nature 506, 102–106. doi: 10.1038/nature12720

PubMed Abstract | CrossRef Full Text | Google Scholar

Paton, A. W., Beddoe, T., Thorpe, C. M., Whisstock, J. C., Wilche, M. C., Rossjohn, J., et al. (2006). AB5 subtilase cytotoxin inactivates the endoplasmic reticulum chaperone BiP. Nature 443, 548–552. doi: 10.1038/nature05124

PubMed Abstract | CrossRef Full Text | Google Scholar

Pfeffer, S., Brandt, F., Hrabe, T., Lang, S., Eibauer, M., Zimmermann, R., et al. (2012). Structure and 3D arrangement of endoplasmic reticulum membrane-associated ribosomes. Structure 20, 1508–1518. doi: 10.1016/j.str.2012.06.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Pfeffer, S., Burbaum, L., Unverdorben, P., Pech, M., Chen, Y., Zimmermann, R., et al. (2015). Structure of the native Sec61 protein-conducting channel. Nature Commun. 6:9403. doi: 10.1038/ncomms9403

PubMed Abstract | CrossRef Full Text | Google Scholar

Pfeffer, S., Dudek, J., Gogala, M., Schorr, S., Linxweiler, J., Lang, S., et al. (2014). Structure of the mammalian oligosaccharyl-transferase in the native ER protein translocon. Nat. Commun. 5:4072. doi: 10.1038/ncomms4072

PubMed Abstract | CrossRef Full Text | Google Scholar

Pfeffer, S., Dudek, J., Ng, B., Schaffa, M., Albert, S., Plitzko, J., et al. (2017). Dissecting the molecular organization of the translocon-associated protein complex. Nat. Commun. 8:14516. doi: 10.1038/ncomms14516

PubMed Abstract | CrossRef Full Text | Google Scholar

Pfeffer, S., Dudek, J., Zimmermann, R., and Förster, F. (2016). Organization of the native ribosome-translocon complex at the mammalian endoplasmic reticulum membrane. BBA Gen. Sub. 1860, 2122–2129. doi: 10.1016/j.bbagen.2016.06.024

PubMed Abstract | CrossRef Full Text | Google Scholar

Plumb, R., Zhang, Z.-R., Appathurai, S., and Mariappan, M. (2015). A functional link between the co-translational protein translocation pathway and the UPR. eLife 4:e07426. doi: 10.7554/eLife.07426

PubMed Abstract | CrossRef Full Text | Google Scholar

Potter, M. D., Seiser, R. M., and Nicchitta, C. V. (2001). Ribosome exchange revisited: a mechanism for translation-coupled ribosome detachment from the ER membrane. Trends Cell Biol. 11, 112–115. doi: 10.1016/S0962-8924(00)01905-X

PubMed Abstract | CrossRef Full Text | Google Scholar

Rabu, C., Schmid, V., Schwappach, B., and High, S. (2009). Biogenesis of tail-anchored proteins: the beginning for the end? J. Cell Sci. 122, 3605–3612. doi: 10.1242/jcs.041210

PubMed Abstract | CrossRef Full Text | Google Scholar

Reithinger, J. H., Kim, J. E. H., and Kim, H. (2013). Sec62 protein mediates membrane insertion and orientation of moderately hydrophobic signal anchor proteins in the endoplasmic reticulum (ER). J. Biol. Chem. 288, 18058–18067. doi: 10.1074/jbc.M113.473009

PubMed Abstract | CrossRef Full Text | Google Scholar

Römisch, K. (2005). Endoplasmic reticulum-associated degradation. Annu. Rev. Cell Dev. Biol. 21, 435–456. doi: 10.1146/annurev.cellbio.21.012704.133250

PubMed Abstract | CrossRef Full Text | Google Scholar

Roos, A., Buchlremer, S., Kollipara, L., Labisch, T., Gatz, C., Zitzelsberger, M., et al. (2014). Myopathy in Marinesco-Sjögren syndrome links endoplasmic reticulum chaperone dysfunction to nuclear envelope pathology. Acta Neuropathol. 127, 761–777. doi: 10.1007/s00401-013-1224-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Rutkowski, D. T., Kang, S. W., Goodman, A. G., Garrison, J. L., Taunton, J., Katze, M. G., et al. (2007). The role of p58IPK in protecting the stressed endoplasmic reticulum. Mol. Biol. Cell 18, 3681–3691. doi: 10.1091/mbc.E07-03-0272

PubMed Abstract | CrossRef Full Text | Google Scholar

Schäuble, N., Lang, S., Jung, M., Cappel, S., Schorr, S., Ulucan, Ö., et al. (2012). BiP-mediated closing of the Sec61 channel limits Ca²⁺ leakage from the ER. EMBO J. 31, 3282–3296. doi: 10.1038/emboj.2012.189

PubMed Abstract | CrossRef Full Text | Google Scholar

Schekman, R. (2002). SEC mutants and the secretory apparatus. Nat. Med. 8, 1055–1058. doi: 10.1038/nm769

PubMed Abstract | CrossRef Full Text

Schlenstedt, G., Gudmundsson, G. H., Boman, H. G., and Zimmermann, R. (1990). A large presecretory protein translocates both cotranslationally, using signal recognition particle and ribosome, and posttranslationally, without these ribonucleoparticles, when synthesized in the presence of mammalian microsomes. J. Biol. Chem. 265, 13960–13968.

Google Scholar

Schoebel, S., Mi, W., Stein, A., Ovchinikov, S., Pavlovicz, R., DiMaio, R., et al. (2017). Cryo-EM structure of the protein-conducting ERAD channel Hrd1 in complex with Hrd3. Nature 548, 352–355. doi: 10.1038/nature23314

PubMed Abstract | CrossRef Full Text | Google Scholar

Schorr, S., Klein, M.-C., Gamayun, I., Melnyk, A., Jung, M., Schäuble, N., et al. (2015). Co-chaperone specificity in gating of the polypeptide conducting channel in the membrane of the human endoplamic reticulum. J. Biol. Chem. 290, 18621–11835. doi: 10.1074/jbc.M115.636639

PubMed Abstract | CrossRef Full Text | Google Scholar

Schubert, D., Klein, M.-C., Haßdenteufel, S., Caballero-Oteyza, A., Yang, L., Proietti, M., et al. (2017). Plasma cell deficiency in humans with heterozygous mutations in SEC61A1. J. Allergy Clin. Immunol. 6749, 31265–31274. doi: 10.1016/j.jaci.2017.06.042

CrossRef Full Text

Schuldiner, M., Metz, J., Schmid, V., Denic, V., Rakwalska, M., Schmitt, H. D., et al. (2008). The GET complex mediates insertion of tail-anchored proteins into the ER membrane. Cell 134, 634–645. doi: 10.1016/j.cell.2008.06.025

PubMed Abstract | CrossRef Full Text | Google Scholar

Schwarz, D. S., and Blower, M. D. (2016). The endoplasmic reticulum: structure, function and response to cellular signaling. Cell. Mol. Life Sci. 73, 79–94. doi: 10.1007/s00018-015-2052-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Senderek, J., Krieger, M., Stendel, C., Bergmann, C., Moser, M., Breitbach-Faller, N., et al. (2005). Mutations in Sil1 cause Marinesco-Sjögren syndrome, a cerebellar ataxia with cataract and myopathy. Nat. Gen. 37, 1312–1314. doi: 10.1038/ng1678

PubMed Abstract | CrossRef Full Text | Google Scholar

Shannon, T. R., Ginsburg, K. S., and Bers, D. M. (2000). Reverse Mode of the Sarcoplasmic reticulum calcium pump and load-dependent cytosolic calcium decline in voltage-clamped cardiac ventricular myocytes. Biophys. J. 78, 322–333 doi: 10.1016/S0006-3495(00)76595-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Shao, S., and Hegde, R. S. (2011). A calmodulin-dependent translocation pathway for small secretory proteins. Cell 147, 1576–1588. doi: 10.1016/j.cell.2011.11.048

PubMed Abstract | CrossRef Full Text | Google Scholar

Shibata, Y., Shemesh, T., Prinz, W. A., Palazzo, A. F., Kozlov, M. M., and Rapoport, T. A. (2010). Mechanisms determining the morphology of the peripheral ER. Cell 143, 774–788. doi: 10.1016/j.cell.2010.11.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Shibata, Y., Voeltz, G. K., and Rapoport, T. A. (2006). Rough sheets and smooth tubules. Cell 126, 435–439. doi: 10.1016/j.cell.2006.07.019

PubMed Abstract | CrossRef Full Text | Google Scholar

Simon, S. M., Blobel, G., and Zimmerberg, J. (1989). Large aqueous channels in membrane vesicles derived from the rough endoplasmic reticulum of canine pancreas or the plasma membrane of Escherichia coli. Proc. Natl. Acad. Sci. U.S.A. 86, 6176–6180. doi: 10.1073/pnas.86.16.6176

CrossRef Full Text | Google Scholar

Snapp, E. L., Reinhart, G. A., Bogert, B. A., Lippincott-Schwartz, J., and Hegde, R. S. (2004). The organization of engaged and quiescent translocons in the endoplasmic reticulum of mammalian cells. J. Cell Biol. 164, 997–1007. doi: 10.1083/jcb.200312079

PubMed Abstract | CrossRef Full Text | Google Scholar

Sommer, N., Junne, T., Spiess, M., and Hartmann, E. (2013). TRAP assists membrane protein topogenesis at the mammalian ER membrane. Biochim. Biophys. Acta 1833, 3104–3111. doi: 10.1016/j.bbamcr.2013.08.018

PubMed Abstract | CrossRef Full Text | Google Scholar

Spang, A. (2015). Anniversary of the discovery of sec mutants by Novick and Schekman. Mol. Biol. Cell 26, 1783–1785. doi: 10.1091/mbc.E14-11-1511

PubMed Abstract | CrossRef Full Text | Google Scholar

Stefanovic, S., and Hegde, R. S. (2007). Identification of a targeting factor for posttranslational membrane protein insertion into the ER. Cell 128, 1147–1159. doi: 10.1016/j.cell.2007.01.036

PubMed Abstract | CrossRef Full Text | Google Scholar

Stephens, S. B., Dodd, R. D., Lerner, R. S., Pyhtila, B. M., and Nicchita, C. V. (2008). Analysis of mRNA partitioning between the cytosol and endoplasmic reticulum compartments of mammalian cells. Methods Mol. Biol. 419, 197–214. doi: 10.1007/978-1-59745-033-1_14

PubMed Abstract | CrossRef Full Text | Google Scholar

Sundaram, A., Plumb, R., Appathurai, S., and Mariappan, M. (2017). The Sec61 translocon limits IRE1α signaling during the unfolded protein response. eLife 6:e27187. doi: 10.7554/eLife.27187

PubMed Abstract | CrossRef Full Text | Google Scholar

Synofzik, M., Haack, T. B., Kopaijtich, R., Gorza, M., Rapaport, D., Greiner, M., et al. (2014). Absence of BiP co-chaperone DNAJC3 causes diabetes mellitus and multisystemic neurodegeneration. Am. J. Hum. Gen. 95, 689–697. doi: 10.1016/j.ajhg.2014.10.013

PubMed Abstract | CrossRef Full Text | Google Scholar

Terasaki, M., Shemesh, T., Kasthuri, N., Klemm, R. W., Schalek, R., Hayworth, K. J., et al. (2013). Stacked endoplasmic reticulum sheets are connected by helicoidal membrane motifs. Cell 154, 285–296. doi: 10.1016/j.cell.2013.06.031

PubMed Abstract | CrossRef Full Text | Google Scholar

Tu, H., Nelson, O., Bezprozvanny, A., Wang, Z., Lee, S.-F., Hao, Y.-H., et al. (2006). Presenilins form ER Ca²⁺ leak channels, a function disrupted by familial Alzheimer's disease-linked mutations. Cell 126, 981–993. doi: 10.1016/j.cell.2006.06.059

PubMed Abstract | CrossRef Full Text | Google Scholar

Tyedmers, J., Lerner, M., Wiedmann, M., Volkmer, J., and Zimmermann, R. (2003). Polypeptide-binding proteins mediate completion of co-translational protein translocation into the mammalian endoplasmic reticulum. EMBO Rep. 4, 505–510. doi: 10.1038/sj.embor.embor826

PubMed Abstract | CrossRef Full Text | Google Scholar

Ushioda, R., Miyamoto, A., Inoue, M., Watanabe, S., Okumura, M., Maegawa, K., et al. (2016). Redox-assisted regulation of Ca²⁺ homeostasis in the endoplasmic reticulum by disulfide reductase Erdj5. Proc. Natl. Acad. Sci. U.S.A. 113, E6055–E6063. doi: 10.1073/pnas.1605818113

PubMed Abstract | CrossRef Full Text | Google Scholar

Valm, A. M., Cohen, S., Legant, W. R., Melunis, J., Hershberg, U., Wait, E., et al. (2017). Applying systems-level spectral imaging and analysis to reveal the organelle interactome. Nature 546, 162–167 doi: 10.1038/nature22369

PubMed Abstract | CrossRef Full Text | Google Scholar

Van Coppenolle, F., Van den Abeele, F., Slomianny, C., Flourakis, M., Hesketh, J., Dewailly, E., et al. (2004). Ribosome-translocon complex mediates calcium leakage from endoplasmic reticulum stores. J. Cell Sci. 117, 4135–4142. doi: 10.1242/jcs.01274

PubMed Abstract | CrossRef Full Text | Google Scholar

Vanden Abeele, F., Bidaux, G., Gordienko, D., Beck, B., Panchin, Y. V., Baranova, A. V., et al. (2006). Functional implications of calcium permeability of the channel formed by pannexin 1. J. Cell Biol. 174, 535–546. doi: 10.1083/jcb.200601115

PubMed Abstract | CrossRef Full Text | Google Scholar

Van den Berg, B., Clemons, W. M., Collinson, I., Modis, Y., Hartmann, E., Harrison, S. C., et al. (2004). X-ray structure of a protein-conducting channel. Nature 427, 36–44. doi: 10.1038/nature02218

PubMed Abstract | CrossRef Full Text | Google Scholar

Van Lehn, R. C., Zhang, B., and Miller, I. I. I. T. F. (2015). Regulation of multispanning membrane protein topology via post-translational annealing. ELife 4:e08697. doi: 10.7554/eLife.08607

PubMed Abstract | CrossRef Full Text | Google Scholar

Vermeire, K., Bell, T. W., Van Puyenbroeck, V., Giraut, A., Noppen, S., Liekens, S., et al. (2014). Signal peptide-binding drug as a selective inhibitor of co-translational protein translocation. PLoS Biol. 12:e1002011. doi: 10.1371/journal.pbio.1002011

PubMed Abstract | CrossRef Full Text | Google Scholar

Vilardi, F., Lorenz, H., and Dobberstein, B. (2011). WRB is the recpetor for TRC40/Asna-1-mediated insertion of tail-anchored proteins into the ER membrane. J. Cell Sci. 124, 1301–1307. doi: 10.1242/jcs.084277

CrossRef Full Text | Google Scholar

Vilardi, F., Stephan, M., Clancy, A., Janshoff, A., and Schwappach, B. (2014). WRB and caml are necessary and sufficient to mediate tail-anchored protein targeting to the ER membrane. PLoS ONE 9:e85033. doi: 10.1371/journal.pone.0085033

PubMed Abstract | CrossRef Full Text | Google Scholar

Vishnu, N., Khan, M. J., Karsten, F., Groschner, L. N., Waldeck-Weiermaier, M., Rost, R., et al. (2013). ATP increases within the lumen of the endoplasmic reticulum upon intracellular Ca²⁺ release. Mol. Biol. Cell 25, 368–379. doi: 10.1091/mbc.E13-07-0433

PubMed Abstract | CrossRef Full Text

Voigt, S., Jungnickel, B., Hartmann, E., and Rapoport, T. A. (1996). Signal sequence-dependent function of the TRAM protein during early phases of protein transport across the endoplasmic reticulum membrane. J. Cell Biol. 134, 25–35. doi: 10.1083/jcb.134.1.25

PubMed Abstract | CrossRef Full Text | Google Scholar

von der Malsburg, K., Shao, S., and Hegde, R. S. (2015). The ribosome quality control pathway can access nascent polypeptides stalled at the Sec61 translocon. Mol. Biol. Cell 26, 2168–2180. doi: 10.1091/mbc.E15-01-0040

PubMed Abstract | CrossRef Full Text | Google Scholar

von Heijne, G. (1985). Signal sequences. J. Mol. Biol. 184, 99–105. doi: 10.1016/0022-2836(85)90046-4

PubMed Abstract | CrossRef Full Text | Google Scholar

von Heijne, G. (1986). Towards a comparative anatomy of N-terminal topogenic protein sequences. J. Mol. Biol. 189, 239–242. doi: 10.1016/0022-2836(86)90394-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Voorhees, R. M., and Hegde, R. S. (2015). Structures of the scanning and engaged states of the mammalian SRP-ribosome complex. Elife 4:e07975. doi: 10.7554/eLife.07975

PubMed Abstract | CrossRef Full Text | Google Scholar

Voorhees, R. M., and Hegde, R. S. (2016). Structure of the Sec61 channel opened by a Signal Sequence. Science 351, 88–91. doi: 10.1126/science.aad4992

PubMed Abstract | CrossRef Full Text | Google Scholar

Voorhees, R. M., Fernández, I. S., Scheres, S. H. W., and Hegde, R. S. (2014). Structure of the mammalian ribosome-Sec61 complex to 3.4 Å resolution. Cell 157, 1632–1643. doi: 10.1016/j.cell.2014.05.024

PubMed Abstract | CrossRef Full Text | Google Scholar

Wada, I., Rindress, D., Cameron, P. H., Ou, W.-J., Doherty, I. I., Louvard, D., et al. (1991). SSRα and associated calnexin are major calcium binding proteins of the endoplasmic reticulum. J. Biol. Chem. 266, 19599–19610.

PubMed Abstract | Google Scholar

Walter, P., and Blobel, G. (1981). Translocation of proteins across the endoplasmic reticulum. II. Signal recognition protein, SRP, mediates the selective binding to microsomal membranes of in-vitro-assembled polysomes synthesizing secretory protein. J. Cell Biol. 91, 551–556. doi: 10.1083/jcb.91.2.551

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, Q., Liu, Y., Soetandyo, N., Baek, K., Hegde, R., and Ye, Y. (2011). A ubiquitin ligase-associated chaperone holdase maintains polypeptides in soluble states for proteasome degradation. Mol. Cell 42, 758–770. doi: 10.1016/j.molcel.2011.05.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Wiedmann, B., Saki, H., Davis, T. A., and Wiedmann, M. (1994). A protein complex required for signal-sequence-specific sorting and translocation. Nature 370, 434–440. doi: 10.1038/370434a0

PubMed Abstract | CrossRef Full Text | Google Scholar

Wirth, A., Jung, M., Bies, C., Frien, M., Tyedmers, J., Zimmermann, R., et al. (2003). The Sec61p complex is a dynamic precursor activated channel. Mol. Cell 12, 261–268. doi: 10.1016/S1097-2765(03)00283-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Wuytack, F., Raeymaekers, L., and Missiaen, L. (2002). Molecular physiology of the SERCA and SPCA pumps. Cell Calc. 32, 279–305. doi: 10.1016/S0143416002001847

PubMed Abstract | CrossRef Full Text | Google Scholar

Yamamoto, Y., and Sakisaka, T. (2012). Molecular machinery for insertion of tail-anchored membrane proteins into the endoplasmic reticulum membrane in mammalian cells. Mol. Cell 48, 387–397. doi: 10.1016/j.molcel.2012.08.028

PubMed Abstract | CrossRef Full Text | Google Scholar

Yanagitani, K., Kimata, Y., Kadokura, H., and Kohno, K. (2011). Translational pausing ensures membrane targeting and cytoplasmic splicing of Xbp1u Mrna. Science 331, 586–589. doi: 10.1126/science.1197142

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, B., and Miller, T. F. III (2012). Long-timescale dynamics and regulation of Sec-facilitated protein translocation. Cell Rep. 2, 927–937. doi: 10.1016/j.celrep.2012.08.039

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, K., and Kaufman, R. J. (2004). Signaling the unfolded protein response from the endoplasmic reticulum. J. Biol. Chem. 279, 25935–25938. doi: 10.1074/jbc.R400008200

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, S. L., Yeromin, A. V., Zhang, X. H., Yu, Y., Safrina, O., Penna, A., et al. (2006). Genome-wide RNAi screen of Ca²⁺ influx identifies genes that regulate Ca²⁺ release-activated Ca²⁺ channel activity. Proc. Natl. Acad. Sci. U.S.A. 103, 9357–9362. doi: 10.1073/pnas.0603161103

CrossRef Full Text | Google Scholar

Zhao, L., Longo-Guess, C., Harris, B. S., Lee, J.-W., and Ackerman, S. L. (2005). Protein accumulation and neurodegeneration in the woozy mutant mouse is caused by disruption of SIL1, a cochaperone of BiP. Nat. Gen. 37, 974–979. doi: 10.1038/ng1620

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhao, Y., Hu, J., Miao, G., Qu, L., Wang, Z., Li, G., et al. (2013). Transmembrane protein 208: a Novel ER-localized protein that regulates autophagy and er stress. PLoS ONE 8:e64228. doi: 10.1371/journal.pone.0064228

PubMed Abstract | CrossRef Full Text | Google Scholar

Zimmermann, R. (2016). Components and mechanisms of import, modification, folding, and assembly of immunoglobulins in the endoplasmic reticulu. J. Clin. Immunol. 36(Suppl. 1), 5–11. doi: 10.1007/s10875-016-0250-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Zimmermann, R., Eyrisch, S., Ahmad, M., and Helms, V. (2011). Protein translocation across the ER membrane. Biochim. Biophys. Acta 1808, 912–924. doi: 10.1016/j.bbamem.2010.06.015

PubMed Abstract | CrossRef Full Text | Google Scholar