Peter Buchwald1,2*- 1Diabetes Research Institute, Miller School of Medicine, University of Miami, Miami, FL, United States
- 2Department of Molecular and Cellular Pharmacology, Miller School of Medicine, University of Miami, Miami, FL, United States
Blocking protein-protein interactions (PPIs) involved in the initiation of the cell attachment and entry of viruses is an important antiviral mechanism of action including for neutralizing antibodies. Doing it with small-molecule inhibitors (SMIs) is challenging, as it is for all other PPIs, and might require the exploration of chemical space beyond that of typical drug-like structures. However, it could lead to new antiviral agents suitable for oral administration and acting on alternative targets, considerations that are essential for the development of widely acceptable and broad-spectrum preventive or curative therapeutics. Fostemsavir, an antiretroviral that acts via blocking of the gp120–CD4 PPI, supports the feasibility of the concept. Here, a brief review of relevant drug design considerations is presented together with a summary of the progress made toward the identification of SMIs targeting the PPI between the SARS-CoV-2 spike protein and ACE2 that initiates the viral attachment and cellular entry of this coronavirus causing the COVID-19 pandemic. SMIs identified in various screening assays that were also confirmed to have antiviral activity in a live virus or pseudovirus assay with an IC50 < 30 µM so far include several organic dyes (methylene blue, Evans blue, Congo red, direct violet 1), verteporfin, DRI-C23041, and cannabigerolic and cannabidiolic acids. While specificity and activity profiles still need improvement, results so far already provide proof-of-principle evidence for the feasibility of SMIs targeting the SARS-CoV-2-S–hACE2 PPI. Methylene blue, which is approved for clinical use, is orally bioactive, and could act by multiple mechanisms of action, might have potential for repurposing for COVID-19 prevention and treatment.
Introduction
New drugs introduced during the past century, such as antibacterials (penicillin, 1943) anti-inflammatories (cortisol, 1952), antipsychotics (chlorpromazine, 1953), contraceptives (norethindrone, 1960), anxiolytics (diazepam, 1963), immunosuppressant (cyclosporin A, 1983), antidepressants (fluoxetine, 1987), TNFα-inhibitors (infliximab, 1998), and PD-1–PD-L1 inhibitors (pembrolizumab, nivolumab, 2014)—all shown with their first year of US market approval, are responsible for most of the unprecedented medical progress that happened since then and have completely altered the way life is conducted in industrialized nations. However, truly effective antivirals are still lacking, as the recent coronavirus-inflicted COVID-19 pandemic made painfully clear. The search for antivirals has its own particular challenges, as viruses hijack the reproduction machinery of their host organisms, but progress in drug discovery and development as a whole has been frustratingly slow due to a variety of problems (Proudfoot, 2002; Munos, 2009; Paul et al., 2010; Scannell et al., 2012).
Despite enormous increases in research and development (R&D) investments, the number of newly introduced drugs in the United States remained stubbornly stagnant since the 1960s staying around 20–30 per year (Figure 1) and ∼85% of them represented no or only modest improvements (Wolff, 1995) demonstrating a pervasive need for innovation. This is probably best illustrated by the fact that the number of new drugs approved by the United States Food and Drug Administration (FDA) that were developed per $1 billion of R&D spending in the drug industry (inflation-adjusted) has been decreasing exponentially since 1950, being steadily halved about every 9 years (Scannell et al., 2012). This is mainly due to the highly increased regulatory burden, the unrealistic public expectation of no side effects, the need to outperform existing old drugs, and the depletion of effective new targets for traditional drug design approaches (Walters et al., 2011; Bodor and Buchwald, 2012; Scannell et al., 2012). Regarding the last, it is commonly estimated that there are only about 500 to 1,500 human protein targets that are both “druggable” and “disease modifying”, i.e., only about 2–7% of the ∼20,000 canonical (nonmodified) human proteins encoded by individual genes (Hopkins and Groom, 2002; Russ and Lampel, 2005). In general agreement with this, a survey of small-molecule drug targets counted ∼550 human proteins (plus another ∼180 non-human ones) (Santos et al., 2017). Thus, we are probably beginning to run out of traditional protein targets, at least human ones, and quite likely most low-hanging fruits among such targets that can provide therapeutic benefits have already been picked.
FIGURE 1. The number of all new drugs launched annually in the United States with FDA approval. The number of all new drugs are shown as blue columns with that of new biologics (approved biologic license applications, BLAs) as superimposed green columns. Except for a few peaks in the 1950s, 1990s, and the last decade, it has been quite steady in the 20–30 per year range. Graphic prepared based on data from (Reuben, 1996; Mullard, 2016a; 2020).
Small-Molecule Inhibitors of Protein-Protein Interactions
Protein-protein interactions (PPIs), the focus of the present review, represent possible additional, alternate targets as evidenced by the increasing number of clinically approved biologics targeting them (Figure 1). For example, one of the latest such successes was the development of cancer immunotherapies targeting immune checkpoint PPIs such as CD80–CTLA4 and PD-1–PD-L1, which has been named Science Breakthrough of the Year in 2013 (Couzin-Frankel, 2013). Unfortunately, PPIs are difficult to modulate with small molecules as the corresponding protein interfaces tend to lack well-defined ligand-binding sites where sufficiently strong interactions can take place to ensure the energy of interaction needed for high affinity binding. Nevertheless, the sheer number of such PPIs, estimated to be in the 300,000 (Zhang et al., 2012; Cheng et al., 2018) to 650,000 (Stumpf et al., 2008) range for humans, implies that a considerable number should still be druggable. Drugs need to be quite potent to be able to compete with naturally present ligands, to be sufficiently specific for their intended target, and to not need unacceptably high doses. Typically, they need to have affinities in the mid-nanomolar range. For example, the median value for all approved drugs has been estimated to be around 20 nM (Overington et al., 2006), which corresponds to a free energy of binding of ΔG0 = –RT·lnKD = –5.94·log10KD [kJ/mol] = 45.7 kJ/mol. To achieve such high energy, small-molecule endogenous agonists and drugs of classic targets such as G-protein coupled receptors (GPCRs) typically bind at binding sites that are fully buried and allow interactions along the entire ligand surface (Figure 2A) (Buchwald, 2019). Since PPI interfaces tend to be relatively large and flat surfaces that lack such well-defined deep pockets, strong binding is difficult to achieve here with small molecules, as interactions are limited to only parts of the total ligand surface. This is illustrated in Figure 2, which compares the 3D structure of a typical fully buried small-molecule agonist at a classic GPCR target (purinergic P2Y12 receptor) with that of a surface-bound small-molecule inhibitor (SMI) of a PPI (venetoclax bound to BCL-2).
FIGURE 2. Comparing the binding of small-molecule drugs at PPI interface to that at classic targets such as G-protein coupled receptors (GPCRs). (A) 3D structure of the purinergic P2Y12 receptor (a type Aδ GPCR) with an agonist (2MeSADP). Protein structure (PDB ID# 4PXZ (Zhang et al., 2014)) is shown covered with a semi-transparent gray surface; the ligand is shown as darker CPK structure. Two different perspectives are included with the one on the right being a 90° rotated and somewhat enlarged view. Here, the receptor-bound ligand is faded as it fully buried inside the receptor and obscured by the covering surface. (B) 3D structure of BCL-2 (a pro-survival protein targeted in cancer therapeutics) with an FDA-approved SMI of PPI (venetoclax). Structure (PDB ID# 6O0K (Birkinshaw et al., 2019)) is shown as before; however, here the bound PPI inhibitor is barely buried leaving large parts of its surface exposed as indicated by the more vivid colors where directly visible.
Not surprisingly, binding pockets on protein-protein interfaces that are suitable to accommodate small molecules are indeed considerably smaller than those of traditional protein-ligand interactions (Fuller et al., 2009). Typically, existing drugs target a single binding pocket with an average volume of ∼300 Å3, whereas SMIs of PPIs target multiple (3–5) smaller pockets (∼100 Å3) (Fuller et al., 2009). As the achievable maximum energy is limited by the pocket size (Buchwald, 2008), adequate binding affinity at protein interfaces can only be achieved by molecules large enough to reach a sufficient number of such smaller pockets (as illustrated in Figure 2B). The need for larger size can also be seen from the perspective of ligand efficiency, LE, defined as the binding energy per unit size–typically the binding free energy per non-hydrogen atom (Na), LE = ΔG0/Na (Hopkins et al., 2004). Typical ligand-receptor protein interactions have LE of ∼1.5 kJ/atom (Hopkins et al., 2004; Hajduk, 2006; Reynolds et al., 2007; Buchwald, 2008), which corresponds to an about two-fold increase in affinity (decrease in KD or IC50) with the addition of each (non-hydrogen) atom. Such high LE is almost impossible to achieve at PPI interfaces where the bound SMI ligand can interact only along part of its surface (Figure 2B). Thus, to achieve the free energy needed for 20 nM binding (45.7 kJ/mol) with an LE of 1 kJ/atom, structures with more than 45 non-hydrogen atoms are needed, which is already larger than desired for typical “druggability”. SMIs of PPIs were indeed found to be larger than classic drugs including receptor ligands, ion channel modulators, and enzyme inhibitors (Neugebauer et al., 2007).
On the other hand, biologics, such as antibodies and fusion proteins, can interact with proteins along a broader surface and a variety of epitopes without having to rely solely on druggable pockets to achieve adequate affinity and specificity. An increasing number of biologics are being used clinically as they can be highly specific (Figure 1); however, they cannot cross cell membranes, thus cannot reach intracellular targets (Verdine and Walensky, 2007; Hughes et al., 2011; Neklesa et al., 2017), and their protein nature also causes solubility, stability, route of administration (i.e., no oral bioavailability), and biodistribution limitations. Further, since they are foreign proteins, they can act as antigens and elicit strong immune responses in some recipients (Suntharalingam et al., 2006; Wadman, 2006; Leader et al., 2008). All these problems are further exacerbated by their typically long elimination half-lives, which makes it difficult to rapidly eliminate unwanted effects when they occur (Huck et al., 2018). Not surprisingly, FDA-approved biologics encountered more post-market safety issues than did small-molecule drugs (Downing et al., 2017). SMIs of PPIs may represent viable alternatives lacking these problems, if the difficulties related to affinity/specificity can be overcome. While such SMIs were not pursued until relatively recently because they were considered unlikely to be successful due to the aforementioned challenges, during the last 2 decades, it has become clear that SMIs can be effective against at least some PPIs. Most small-molecule PPI modulators are SMIs (i.e., antagonists)—our sole focus here, as so far there are only a limited number of identified small-molecule PPI ‘agonists’ (i.e., enhancers or stabilizers) (Thiel et al., 2012; Milroy et al., 2014; Andrei et al., 2017). SMIs of PPIs, as antagonists in general, can be orthosteric, directly interfering with the interface and competing with the protein ligand, or allosteric, binding away from the interface but causing sufficient conformational change to block binding of the protein ligand.
Tens of PPI-targeting SMIs have reached preclinical development (Arkin and Wells, 2004; Wells and McClendon, 2007; Wilson, 2009; Buchwald, 2010; Arkin et al., 2014; Milroy et al., 2014; Song and Buchwald, 2015; Scott et al., 2016), and three are approved by the FDA for clinical use: lifitegrast (Gadek et al., 2002), venetoclax (Souers et al., 2013), and fostemsavir (Meanwell et al., 2018) (Figure 3). Lifitegrast (SAR 1118) is a LFA-1–ICAM-1 inhibitor developed first at Sunesis (Zhong et al., 2012) from a series originating at Genentech (Gadek et al., 2002) and then clinically by SARcode/Shire; it was approved by the FDA for the treatment of dry eye in 2016 (Xiidra) (Scott et al., 2016). Venetoclax (ABT-199) is part of a small-molecule series developed by Abbott and later AbbVie and designed to target PPIs in the B cell lymphoma 2 (BCL-2) family (Souers et al., 2013). It received FDA approval in 2015 for treatment of chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), and later acute myeloid leukemia (AML) (Venclexta, Venclyxto) (Mullard, 2016b). Fostemsavir (BMS-663068) is a water soluble prodrug of temsavir developed by Bristol-Myers Squibb that acts by blocking gp120 binding to CD4 to limit HIV attachment and entry; it was approved by the FDA for clinical use in the US in 2020 as an antiretroviral for adults living with HIV/AIDS (Rukobia) (Meanwell et al., 2018). Finally, maraviroc (Selzentry) is an antiretroviral that can be considered an allosteric SMI of the gp120–CCR5 PPI as it targets CCR5 and stabilizes a conformation no longer recognized by the HIV envelope (Melby and Westby, 2009; Tan et al., 2013). These successes, and particularly that of fostemsavir reemphasize the feasibility of SMIs of PPIs as drug discovery strategy for antivirals. Such SMIs could yield novel therapies that are not only more patient friendly than antibodies (i.e., suitable for oral or inhaled administration), but also less immunogenic, more controllable (shorter half-life/better biodistribution), and possibly even less strain- and mutation-sensitive.
FIGURE 3. SMIs of PPIs approved for clinical use by the FDA. In addition to lifitegrast (an LFA-1–ICAM-1 inhibitor) and venetoclax (a BCL-2–BIM/BAK inhibitor), they include two anti (retro)virals: maraviroc, an allosteric CCR5 inhibitor, and fostemsavir, a prodrug of temsavir, a gp-120–CD4 PPI inhibitor.
Targeting SARS-CoV-2 Spike PPIs as Antiviral Strategy
SARS-CoV-2—Background
While human coronaviruses (CoVs), enveloped positive-stranded RNA viruses mostly responsible for upper respiratory and digestive tract infections, have been circulating for long, SARS-CoV-2 (severe acute respiratory syndrome-coronavirus 2), the most recent one to emerge, became particularly infamous by being the most infectious agent in a century (Tiwari et al., 2020) and the one responsible for the COVID-19 pandemic that caused hundreds of millions of infections and millions of deaths worldwide (Matheson and Lehner, 2020; Shang et al., 2021; V'Kovski et al., 2021). SARS-CoV-2 is one of the seven CoVs known to infect humans, four of which (HCoV 229E, OC43, NL63, and HKU1) are responsible for about a third of the common cold cases and three that are highly pathogenic and caused recent epidemics associated with considerable mortality: SARS-CoV(-1) (2002–2003, ∼10% mortality), MERS-CoV (2012, ∼35% mortality), and now SARS-CoV-2 (2019-), which is less lethal but more transmissible (Guy et al., 2020; Rajgor et al., 2020). While estimates vary, about 3% of the individuals infected with the original SARS-CoV-2 strain needed hospitalization, and the average infection fatality ratio (IFR, percentage of those infected that do not survive) was around 0.5% but in a strongly age-dependent manner increasing exponentially from 0.001 to 0.002% in <20 years old to 10–20% in those >80–90 years old (Salje et al., 2020; O'Driscoll et al., 2021; COVID-19 Forecasting Team, 2022). While difficult to estimate due to changes in vaccination status and treatment options (Bhattacharyya and Hanage, 2022), it has been considerably, several-fold reduced with the more later emerged omicron (B.1.1.529) variant, but likely remained higher than that of influenza (IFR << 0.1%) (Liu et al., 2022; Matsuyama, 2022).
CoVs, which are classified into four genera (α-, ß-, γ-, and δ-CoV), initiate infection with the binding of their spike (S) protein to cell surface receptors followed by membrane fusion and virus entry. For SARS-CoV(-1) and SARS-CoV-2 (as well as HCoV-NL63), the receptor is angiotensin converting enzyme 2 (ACE2) (Lan et al., 2020; Shang et al., 2020; Sivaraman et al., 2021; Zhang et al., 2021). For MERS-CoV, it is dipeptidyl peptidase 4 (DPP4), and for HCoV-229E, human aminopeptidase N (APN; CD13) (V'Kovski et al., 2021). Some ß-coronaviruses (e.g., HCoV-OC43) bind to sialic acid receptors (Tortorici et al., 2019). Thus, blockade of the SARS-CoV-2-S–hACE2 PPI can disrupt infection efficiency, and abrogation of this interaction is a main goal in the development of vaccines and neutralizing antibodies (nAbs) for the COVID-19 pandemic (Jiang et al., 2020; Lv et al., 2020; Tai et al., 2020). In fact, the spike protein is the principal target of nAbs generated following infection by SARS-CoV-2, with the majority of those identified so far recognizing epitopes within the receptor-binding domain (RBD) that binds ACE2 (Sui et al., 2014; Lv et al., 2020; Wang et al., 2020; Wu et al., 2020; Yuan et al., 2020). The spike protein also is the SARS-CoV-2 component of mRNA and adenovirus-based vaccines approved for use (Harvey et al., 2021).
The SARS-CoV-2 spike protein is a homotrimer with monomer units of ∼180 kDa; it is highly glycosylated and is post-translationally cleaved into an S1 and S2 subunit. S1 consists of the amino-terminal domain and the RBD and is responsible for binding to ACE2; S2 includes the trimeric core and is responsible for membrane fusion (Ou et al., 2020; Wang et al., 2020). The RBD located within the S1 domain is known to switch between a standing-up and a lying-down position for receptor binding and immune evasion, respectively (Gil et al., 2020; Shang et al., 2020). Notably, there is a multi-basic furin cleavage site at the S1-S2 boundary, which is unique within b-lineage betacoronaviruses and sarbecoviruses, and is important for the increased infectivity and virulence facilitating the conformational change required for receptor binding (Coutard et al., 2020; Hoffmann et al., 2020; Harvey et al., 2021). It is also an important part of the discussions surrounding the controversies regarding the possible origins of this CoV (Cohen, 2021; Ambati et al., 2022).
There are several possible targets for therapeutic interventions in the CoV lifecycle: viral attachment and entry, uncoating, gRNA replication, translation in ER and Golgi, assembly, and virion release (Guy et al., 2020; V'Kovski et al., 2021; Zhao et al., 2022). Viral attachment and entry are particularly promising among them because they are the first steps in the replication cycle and take place at relatively accessible extracellular sites (Melby and Westby, 2009). They are also well suited for a PPI inhibition focused approach, the subject of the present review. However, targeting viral entry also has its own challenges, as the envelope and fusion glycoproteins are usually the most variable of all virus-encoded proteins. Indeed, the amino acid sequences can vary both within and between individuals, making the spectrum of antiviral activity for any entry inhibitor an important consideration (Melby and Westby, 2009). RNA viruses are known to accumulate mutations over time yielding antibody resistance and requiring the use of antibody cocktails to avoid mutational escape (Baum et al., 2020). Not surprisingly, several SARS-CoV-2 mutants have already emerged some being variants of concern (VOC) with increased transmissibility, higher disease severity, and resistance to neutralizing antibodies, including those elicited by current vaccines (Cai et al., 2021; Gobeil et al., 2021; Harvey et al., 2021; Kupferschmidt, 2021; Wibmer et al., 2021). Currently, as labeled by the WHO, these include alpha (B.1.1.7; first identified in UK, Sep 2020), beta (B.1.351; South Africa, May 2020), gamma (P.1; Brazil, November 2020), delta (B.1.617.2; India, October 2020), and omicron (B.1.1.529; multi/S. Africa, November 2021). Emergence of escape variants is likely to continue as the accumulation of RBD mutations is facilitated by the structural plasticity at the RBD-ACE2 interface, further eroding the activities of therapeutic antibodies and serums of vaccine recipients (Nabel et al., 2022).
Therapeutic Need for Small-Molecule Antivirals
Based on the above, it would be particularly important to have broadly cross-reactive agents that can neutralize a wide range of antigenically disparate viruses (Sui et al., 2014). SARS-CoV(-1) and SARS-CoV-2 share close to 80% amino acid identity in their S proteins, raising the possibility of conserved immunogenic surfaces on these antigens, as supported by the identification of some antibodies of possibly broader activity (Lv et al., 2020; Wec et al., 2020; Starr et al., 2021; Martinez et al., 2022; Park et al., 2022) such as the more recently identified RBD-specific antibody DH1047 (Martinez et al., 2022) or the ACE2-mimicking S2K146 (Park et al., 2022). Nevertheless, most SARS-CoV antibodies are not cross-reactive; for example, none of the 206 RBD-specific monoclonal antibodies derived from single B cells of eight SARS-CoV-2 infected individuals in one study cross-reacted with SARS-CoV(-1) or MERS-CoV RBDs (Ju et al., 2020). As already discussed, targeting such PPIs with SMIs is undoubtedly more challenging, but if successful, it could lead to alternative antiviral treatment options with possible benefits including less strain-specific activity.
Despite the undeniable success of the COVID-19 vaccination program, there remains a considerable need to develop new antivirals and especially oral ones, as a significant portion of the population is either unwilling to be vaccinated or unable to do so due to pre-existing medical conditions. Effective oral treatments could have significant impact on this pandemic as they can be taken easily following the first symptoms. Remdesivir, the first small-molecule COVID-19 drug approved by the FDA, must be given intravenously. Considerable effort and financial resources have been invested in the repurposing of approved drugs as possible small-molecule antiviral agents for SARS-CoV-2, but with only minimal success so far. For example, the large WHO Solidarity trial found that repurposed antiviral drugs including hydroxychloroquine, remdesivir, lopinavir, and interferon-β1 had little or no effect on hospitalized COVID-19 patients, as indicated by overall mortality, initiation of ventilation, and duration of hospital stay (WHO Solidarity Trial Consortium et al., 2020). Further, a paper suggested that most drugs identified in many of the screening assays as possibility for being repurposed against SARS-CoV-2 are not working because they inhibit in the in vitro assay by being cationic amphiphilic drugs that cause phospholipidosis, which, however, does not translate into in vivo activity (Tummino et al., 2021). This observation has been questioned and should be treated with caution as many of these molecules have both in vitro and in vivo efficacy with no reported phospholipidosis (Lane and Ekins, 2021).
Regardless, there is an ongoing need to not just repurpose existing drugs but develop novel ones that can combat such infections (Zhao et al., 2022). Recently, two new drugs with classic antiviral mechanisms (i.e., inhibition of protease activity or viral reproduction) have shown promise and granted emergency use authorization by the United States Food and Drug Administration (FDA) for the treatment of COVID-19: molnupiravir (Jayk Bernal et al., 2021) and nirmatrelvir (part of the nirmatrelvir/ritonavir combination Paxlovid) (Owen et al., 2021). Molnupiravir is a prodrug of the synthetic nucleoside derivative N4-hydroxycytidine that exerts antiviral action through introduction of copying errors during viral RNA replication. It was developed originally for the treatment of influenza at Emory University and acquired by Ridgeback Biotherapeutics, who later partnered with Merck (Jayk Bernal et al., 2021). Nirmatrelvir (PF-07321332) is an inhibitor of the SARS-CoV-2 main protease (Mpro) developed at Pfizer starting from PF-00835231, an inhibitor of recombinant SARS-CoV(-1) Mpro identified during the response to the 2002 SARS outbreak (Owen et al., 2021). It showed very promising clinical results as Paxlovid (nirmatrelvir/ritonavir). In addition, AT-527, a double prodrug of a guanosine nucleotide analog, derived from Atea Pharmaceuticals’ nucleotide prodrug platform and shown to be efficacious and well tolerated in hepatitis C virus (HCV) infected subjects (Good et al., 2021), was also pursued, but it was not successful in its first clinical trial. Lessons learned from RNA viruses so far proved that the size and quality of existing antiviral libraries needs to be increased and diversified and polymerase and protease drugs need to be complemented with others targeting different viral proteins (Edwards et al., 2022).
Small-Molecule PPI Targeting Approaches
Following the outbreak of COVID-19, due to the immense therapeutic need generated by the pandemic it created, tremendous screening and drug discovery efforts were invested into the identification of effective preventive or therapeutic antiviral interventions in both academic and industrial settings (Ghosh et al., 2020; Shyr et al., 2020; Xiu et al., 2020; Su et al., 2021; Zhao et al., 2022). Here, those directed at identifying SMIs of the SARS-CoV-2-S–hACE2 PPI will be highlighted briefly; some of the earliest ones have been summarized in (Chang et al., 2021). Various screening campaigns have been conducted aiming to identify promising hits mainly from repositionable (repurposable) drug and existing chemical libraries. Assays used (often after virtual screening, i.e., in silico preselection typically via molecular docking in AutoDock or Glide) included ELISA (enzyme-linked immunosorbent assay) types (Carino et al., 2020; Bojadzic et al., 2021b; Fu et al., 2021), AlphaLISA (Hanson et al., 2020), Luminex bead-based (Tsegay et al., 2021), surface plasmon resonance (SPR) (Day et al., 2021; Yu et al., 2021; Zhu et al., 2021), affinity selection-mass spectrometry (van Breemen et al., 2022), NanoBiT (Xiong et al., 2021; Yu et al., 2021), CEBIT (condensate-aided enrichment of biomolecular interactions in test tubes) (Pei et al., 2022), and others. Some possible natural product inhibitor have been highlighted in (Ma et al., 2021); however, most are just molecular docking based hypotheses. Considering that several publications relied solely on in silico derived hypotheses or just one in vitro (often cell-free) inhibitory assay, here, only those compounds will be highlighted first that inhibited this PPI in vitro and have concentration-dependent antiviral activity confirmed in a live virus or pseudovirus assay with a sufficiently promising IC50.
In fact, following the emergence of the SARS-CoV(-1) epidemic in the early 2000s, a few groups already performed high-throughput screening (HTS) assays to identify possible antiviral candidates targeting various early steps in its cell invasion. As part of this, some putative SMI candidates of viral entry have been identified, including, for example, SSAA09E2 (from a screening using a SARS/HIV-luc pseudotyped virus infection assay; pseudovirus IC50 9.7 μM) (Adedeji et al., 2013) and VE607 (from a screening using protection from SARS-CoV-induced cytopathic effects, CPE, in Vero cells as a phenotypic indicator; live virus IC50 1.6 μM) (Kao et al., 2004) (see structures in Figure 4). Other inhibitory small-molecule candidates acting by different mechanism have also been identified; they include, for example, SSAA09E1, SSAA09E3 (Adedeji et al., 2013); MP576, HE602 (Kao et al., 2004); ARB 05–018137, ARB 05–090614 (Severson et al., 2007); K22 (Lundin et al., 2014); and others–see reviews in (Du et al., 2009; Gil et al., 2020; Xiu et al., 2020). Most of these had low micromolar activity (Xiu et al., 2020); however, none of them led to approved preventive or curative therapies for human CoV diseases mainly because in addition to their relatively low (i.e., not nanomolar) potency, they were also not particularly suitable for clinical translatability. They could not pass the preclinical development stage and enter clinical trials due to their poor bioavailability, safety, and pharmacokinetics (Xiu et al., 2020).
FIGURE 4. Compounds identified before the COVID-19 pandemic as possible SMIs of the SARS-CoV(-1)-S–hACE2 PPI. SSAA09E2 and VE607 have been identified as viral entry inhibitors for SARS-CoV(-1) with low micromolar activity, see text for details.
SMIs of the SARS-CoV-2-S–hACE2 PPI with confirmed antiviral activity in a live virus or pseudovirus assay having IC50 < 30 µM are from the studies listed below in approximate chronological order of their corresponding publications (structures shown in Figure 5). Whenever possible, therapeutic (selectivity) index (TI, SI) estimates are also included as an indicator of the relative safety, as it quantifies the separation between toxic and effective concentrations, TI = TC50/IC50.
• A computational screening interrogating 57,641 compounds followed by SPR screening of a library of 3,141 compounds by Day and co-workers at Griffith University, Australia identified three candidates showing concentration-dependent antiviral activity in vitro: Evans blue, lifitegrast (Figure 3), and lumacaftor (Day et al., 2021) (March 2021). Of these, Evans blue was the most promising candidate and the only one with IC50 < 30 μM; it had a KD of 2 μM for SARS-CoV-2-S and inhibited SARS-CoV-2 infection in Vero E6 cells with an IC50 of 28 μM. According to the authors, it was also non-toxic for up to 1 mM (TC50 > 1,000 μM), suggesting a sufficiently large therapeutic index (TI > 30).
• Our work at the University of Miami, Florida, United States identified several organic dyes (Congo red, direct violet 1, Evans blue) and novel druglike compounds (DRI-C23041, DRI-C91005) that inhibited the interaction of ACE2 with the spike proteins of SARS-CoV-2 as well as SARS-CoV(-1) with low micromolar activity in cell-free ELISA-type assays (IC50’s of 0.2–3.0 μM) (Bojadzic et al., 2021b) (May 2021). Of these, DRI-C23041, Congo red, and direct violet 1 (Figure 5) were also confirmed to inhibit the entry of two different spike-bearing pseudoviruses into HEK293/Vero E6 cells with IC50’s of 5.6/7.4, 20.3/27.4, and 35.8/16.4 μM, respectively. They were also relatively noncytotoxic in the same assay having TC50 > 400 μM for DRI-C23041 (i.e., TI > 70) and >100 μM for Congo red and direct violet 1 (TI > 5). Evans blue, which was the best hit in the work from Day, was identified as an inhibitor, but was not tested here in viral assays as other compounds were more active.
• During this screening, we also identified methylene blue as a SMI and confirmed that it had a quite promising IC50 of 3.5 μM in this viral assay (Bojadzic et al., 2021a) (January 2021). This is of possible interest as a methylene blue is an inexpensive and widely available drug approved by the FDA for the treatment of methemoglobinemia and used for other medical applications. It was also identified by several other groups as having anti-SARS-CoV-2 activity and confirmed to have low micromolar activity in concentration-response studies including with live viruses, possibly due to additional multiple mechanisms of action (Gendrot et al., 2020; Cagno et al., 2021; Gendrot et al., 2021; Murer et al., 2022). Methylene blue seems to be a promiscuous PPI inhibitor with low micromolar activity and a relatively narrow TI, but with multiple evidence suggesting that it clearly inhibits SARS-CoV-2 including VOCs such as delta (B.1.617.2) (Chuang et al., 2022).
• Fu and co-workers at the New York University School of Medicine, United States screened a library of 958 FDA-approved drugs using ELISA-based HTS, and identified five drugs, N-acetylcysteine (NAC), tiopronin (TPR), verteporfin (VP), calcitriol, and racecadotril, to inhibit RBD–ACE2 interaction at both low and high concentrations (Fu et al., 2021) (July 2021). Of these, verteporfin (Visudyne) significantly inhibited pseudovirus entry into hACE2 overexpressing HEK293T cells (IC50 < 0.1 μM) while having a half cytotoxic concentration TC50 ≈ 10 μM (implying TI > 100). Before this work, verteporfin was confirmed by another group to potently inhibit the cytopathic effect produced by SARS-CoV-2 infection with an IC50 < 0.31 μM with indications that the porphyrin ring structure binds the ACE2 receptor (Gu et al., 2021) (December 2020).
• Xiong and co-workers at the Chinese Academy of Sciences, Shanghai and Beijing, China and collaborators virtually screened and filtered compounds from the SPECS database and then purchased 109 selected candidates for follow-up biological testing including NanoBiT and SPR assays to check their ability to block the SARS-CoV-2-S-RBD–ACE2 PPI (Xiong et al., 2021) (Sep 2021). From these, they highlighted two inhibitors as sufficiently promising in pseudovirus assays with some separation between efficacy and cytotoxicity: DC-RA016 (ZINC125276) (IC50 = 22.4 μM) and DC-RA052 (IC50 = 68 μM). The IC50 for DC-RA016 was, however, somewhat overstated due to the way the concentration-response curve was fitted (with a non-zero bottom) as this compound barely caused 50% inhibition at 100 μM (Figure 4B in (Xiong et al., 2021)). Nevertheless, its structure was included here for illustration (Figure 5).
• Finally, van Breeman and co-workers at Oregon State University, Corvallis, OR, United States used affinity selection-mass spectrometry for the discovery of botanical ligands to the SARS-CoV-2 spike protein and found cannabinoid acids from hemp (Cannabis sativa) to be allosteric as well as orthosteric ligands with micromolar affinity for the spike protein (van Breemen et al., 2022) (January 2022). In follow-up virus neutralization assays, cannabigerolic acid and cannabidiolic acid prevented infection of human epithelial cells by a pseudovirus expressing the SARS-CoV-2 spike protein and prevented entry of live SARS-CoV-2 into cells including for variants B.1.1.7 and B.1.351 with IC50’s of 21 and 23 μM (7.7 and 8.4 μg/ml) in the pseudovirus and 67 and 103 μM (24 and 37 μg/ml) in the live virus assay for cannabidiolic and cannabigerolic acid, respectively, where their cytotoxicities were not yet significant (van Breemen et al., 2022). Cannabidiolic acid seems to have a TC50 around 80 μg/ml (Fig. S4 in (van Breemen et al., 2022)) giving TI ≈ 10.
FIGURE 5. Compounds identified so far since the outbreak of COVID-19 as possible SMIs of the SARS-CoV-2-S–hACE2 PPI. Only compounds that have been confirmed to have antiviral activity in a live virus or pseudovirus assay with promising enough activity (IC50 < 30 µM) are shown.
Some of the other works that identified SMI hits but did not include confirmation in viral assay or the inhibitory activity in these assays was not sufficiently potent include (again, in chronological order of their corresponding publications):
• Carino and co-workers at the University of Perugia, Italy used in silico prescreening followed by in vitro confirmation using a commercial SARS-CoV-2 spike inhibitor screening assay kit and found that naturally occurring and clinically available triterpenoids, such as glycyrrhetinic and oleanolic acids, as well as primary and secondary bile acids and their amidated derivatives, such as glyco-ursodeoxycholic acid and semi-synthetic derivatives such as obeticholic acid, reduced the RBD–ACE2 binding (Carino et al., 2020) (October 2020). However, these compounds showed only weak activity and concentration dependence. None of them caused 50% reduction at the highest concentration tested (10 μM). Activities were not confirmed in viral or pseudoviral assays.
• The group of Hanson an co-workers at the National Center for Advancing Translational Sciences (NCATS), National Institutes of Health (NIH), Bethesda, MD, United States used an AlphaLISA assay based HTS of 3,384 small-molecule drugs and preclinical compounds suitable for repurposing and identified 25 possible hits (Hanson et al., 2020) (November 2020). However, of these only corilagin was validated in cherry-picking as showing activity against ACE2−RBD with an IC50 of 5.5 μM, and there was no confirmation in viral assays.
• Zhu and co-workers at Peking Union Medical College, Beijing, China used SPR to screen a library of 960 compounds and identified demethylzeylasteral as having promisingly high affinities for S-RBD and ACE2 (KD of 1.0 and 1.7 μM for S-RBD and ACE2, respectively) (Zhu et al., 2021) (Dec. 2020). In a pseudovirus assay, it inhibited entry of SARS-CoV-2 pseudovirus into HEK293T cells to “a certain extent” at nontoxic concentration (7% inhibition at 0.37 μM).
• Yu and co-workers at the Shanghai University of Traditional Chinese Medicine, Shanghai, China used SPR and NanoBit assays to verify the spike protein-binding activity of compounds selected via virtual screening from traditional Chinese medicines and then their inhibitory activities on SARS-CoV-2-S-RBD–ACE2 PPI (Yu et al., 2021) (May 2021). They found glycyrrhizic acid to be the most efficient and nontoxic broad-spectrum anti-CoV SMI with a KD of 0.87 μM toward SARS-CoV-2-S1 as suggested by SPR, but an IC50 of only 22 μM for disrupting the corresponding PPI in the NanoBiT assessment. There was no confirmation in viral assay.
• Tsegay and co-workers at Seattle Children’s Research Institute, Seattle, WA, United States screened 2,701 compounds from an “FDA-approved drug screening library” for their ability to inhibit the binding of recombinant SARS-CoV-2 spike to hACE2 in a Luminex bead-based assay and identified 56 that inhibited in a concentration-dependent manner (June 2021) (Tsegay et al., 2021). Best SMIs were thiostrepton, oxytocin, nilotinib, and hydroxycamptothecin with IC50’s in the 4–9 μM range, but there were no cell-based activity or toxicity assessments.
• Pei and co-workers from Tsinghua University, Beijing, China used CEBIT to screen 2572 FDA approved drugs for their ability to inhibit this PPI and identified six candidate compounds that were confirmed by SPR to bind with KD of 17–780 μM: varenicline, sennoside A, quercetin, quinacrine, methylene blue, and sunitinib (Pei et al., 2022) (March 2022).
In addition to SMIs, peptide-based inhibitors of PPIs are also a possibility–see (Lee et al., 2019; Wang et al., 2021; Trisciuzzi et al., 2022) for recent reviews. Some peptide disruptors have also been reported for SARS-CoV-2–hACE2, but so far none have been very effective (Gil et al., 2020; Xiu et al., 2020; Zhang et al., 2020). A stapled peptide approach carried out at the University of Southern Denmark, Odense, Denmark showed some promise with an IC50 of 3.6 μM for inhibition of the PPI, but no cell-based confirmations were performed (Maas et al., 2021). Relatively high affinity peptide binders of the SARS-CoV-2 spike RBD (KD: 80–970 nM) have been identified by affinity selection-mass spectrometry from a screening of 800 million synthetic peptides at the Massachusetts Institute of Technology (MIT), Cambridge, MA, United States ; however, they turned out to not compete for ACE2 binding (Pomplun et al., 2021). Because of bioavailability, metabolic instability (short half-life), lack of membrane permeability, and other issues, developing peptides into clinically approved drugs is difficult and rarely pursued (Otvos and Wade, 2014; Henninot et al., 2018)—a main reason why we focused here on small-molecule compounds that represent an approach much more likely to ultimately transition into clinical development.
Summary and Outlook
Blocking of PPIs involved in the initiation of cell attachment and entry of CoVs can provide efficient antiviral therapeutics and is the main mechanism of action of biologics such as neutralizing antibodies. SMIs face more challenges to achieve this, as they do for all other PPIs; however, they could lead to new alternative antiviral agents that are suitable for oral administration and act by a different mechanism of action than existing small-molecule antivirals such as protease or viral reproduction inhibitors. Oral bioavailability is highly desirable to achieve widespread usage and compliance (Neklesa et al., 2017), and oral therapeutics are much more suitable for long-term use and/or broadly acceptable preventive use (including for transmission control of viral diseases) than any other routes of administration (Cochrane et al., 1999; Moia et al., 2013). Broadly specific activity is also of considerable interest as it could make possible mutation resistant, multi-strain, or even pan-CoV inhibition. While it is usually difficult if not impossible to achieve with antibodies that tend to be target-specific, it could be more achievable with SMIs. For example, we have shown that while the corresponding antibodies did not cross-react for the human vs. mouse CD40–CD40L PPI, our SMIs did and even maintained similar potencies (Margolles-Clark et al., 2009; Bojadzic and Buchwald, 2019). The impact of SARS-CoV-2 variants on spike and RBD structure and on nAb activity, which could also affect SMIs, has been summarized recently (Nabel et al., 2022). Computational simulations of SARS-CoV-2 spike flexibility and its interactions with other proteins are being carried out and should provide helpful tools for future screening efforts (Pedebos and Khalid, 2022).
SMIs of the SARS-CoV-2-S–hACE2 PPI identified so far and summarized above provide proof-of-principle evidence for the feasibility of such a small-molecule approach, but it remains to be seen if they can ultimately lead to clinically usable therapies as specificity and activity profiles still need improvement. While specific goals vary somewhat depending on the specifics of the project, small-molecule drug candidates are generally expected to have, among others: • potency in at least the hundred-nanomolar range (i.e., IC50 < 100 nM meaning pKi > 7) (the median of existing drugs being ∼20 nM); • adequate selectivity/specificity (>20× versus other targets is a reasonable minimum and >100× is desirable); • good safety profile (TI > 30 and optimally >100 in early studies plus passing of all toxicity studies); • adequate solubility and partition properties (needed to achieve acceptable formulation and desired delivery to the intended target); and • acceptable oral bioavailability and duration of action (somewhat flexible, but oral bioavailability F% > 30% and elimination half-life t1/2 > 4 h are reasonable goals) (Williams, 2005; Smith and O’Donnell, 2007; Bodor and Buchwald, 2012). Some of these are undoubtedly more difficult to achieve with small molecules targeting PPIs than with those targeting classic drug targets such as GPCRs, ion channels, and enzymes that have pre-formed domains (pockets) to bind their natural ligands with good affinity and specificity. Problems related to lack of good binding pockets and thus a relatively low ligand efficiency (LE) have been reviewed briefly earlier (Small-Molecule Inhibitors of Protein-Protein Interactions; see also illustration in Figure 2). Because of this, SMIs of PPIs tend to be larger structures than classic drugs (Neugebauer et al., 2007), and it is now well-recognized that the chemical space of existing drugs and corresponding screening libraries does not correspond well with that of promising SMIs of PPIs (Pagliaro et al., 2004; Neugebauer et al., 2007; Reynès et al., 2010; Sperandio et al., 2010; Morelli et al., 2011). Fortunately, computational prescreening including exploration of relevant physicochemical properties can provide valuable information (Villoutreix et al., 2012; Trisciuzzi et al., 2019) and there are now databases, such as TIMBAL (Higueruelo et al., 2009), 2P2I (Bourgeas et al., 2010), or iPPI-DB (Labbe et al., 2016; Torchet et al., 2021), that contain an increasing number of 3D structures for protein-protein and protein-inhibitor complexes. These can make computationally enriched library selection much more successful, which has been shown to accelerate hit discovery (Milhas et al., 2016). A chemical library of >10,000 compounds dedicated to PPI inhibition has been developed (Fr-PPIChem) and is freely available upon request for experimental screening against PPIs (Bosc et al., 2020).
Larger structures, often with multiple aromatic rings, are usually better suited for effective PPI inhibition (Che et al., 2006; Fletcher and Hamilton, 2006; Hershberger et al., 2007); however, these tend to violate the widely used “rule-of-five” (Ro5) criteria, which includes MW < 500 (Lipinski et al., 1997; Lipinski, 2004) and has been widely used to guide candidate selection and ensure adequate oral bioavailability and ADME (absorption, distribution, metabolism, and excretion) profile. Nevertheless, an increasing number of new drugs have been launched lately (including venetoclax and fostemsavir discussed earlier) that significantly violate these empirical rules proving that oral bioavailability can be achieved even in the “beyond the rule-of-five” chemical space (DeGoey et al., 2017; Doak and Kihlberg, 2017). Along these lines, it is instructive to highlight that the first promising lead during the development of venetoclax (ABT-199) was ABT-737, which was so far from being suitable for formulation as a drug that one of its developers jokingly described it as having “the biophysical properties of brick dust” (Mullard, 2016b). Similarly, the incredibly tedious process of medicinal chemistry optimization that was required to make the original lead of the series that ultimately led to fostemsavir (BMS-663068) as a clinical product is nicely described in detail in (Meanwell et al., 2018).
Hits obtained so far for this PPI (Figure 5) reemphasize that our approach relying on the chemical space of organic dyes as a starting point when screening for SMIs of PPIs makes sense. For example, Evans blue which was the best hit identified from a HTS of >3,000 compounds selected after in silico prescreening of ∼60,000 structures (Day et al., 2021), came up as a hit from our screening of a much smaller library of <100 dyes (Bojadzic et al., 2021b). For obvious reasons, organic dyes have good affinity for proteins (Hunger, 2003), and they contain privileged structures for protein binding (Che et al., 2006; Fletcher and Hamilton, 2006; Hershberger et al., 2007). Thus, contrary to commonly available drug-like libraries, they are a good starting point to identify SMIs of PPIs. We have even found organic dyes that are promiscuous PPI inhibitors (Ganesan et al., 2011; Ganesan and Buchwald, 2013). Of course, organic dyes are not particularly suitable for therapeutic development because of their strong color (plus, for azo dyes, their quick metabolic degradation (Levine, 1991; Feng et al., 2012)). Nevertheless, we have shown in at least one case (the CD40–CD40L PPI, a member of the TNF superfamily) that new drug-like SMIs can be developed by first using this chemical space to identify the molecular scaffold required for activity and then removing the color-causing chromophore(s) while retaining PPI inhibitory activity (Chen et al., 2017; Bojadzic et al., 2018). Specificity can be an issue with dyes, and indeed most dyes found here as promising SMIs of the SARS-CoV-2-S–hACE PPI seem to be quite non-specific as the specificity plot shown in Figure 6 illustrates (data from (Bojadzic et al., 2021b)). Also, many azo-containing dyes are likely PAINS (pan-assay interference compounds) that can show up as false positives in screening assays (Baell and Walters, 2014; Aldrich et al., 2017); thus, they need to be treated carefully to ensure, for example, that the PPI inhibitory activity seen is not due to aggregation/polymolecular conglomeration. Nevertheless, medicinal chemistry optimization for specificity should still be feasible, and it is worth remembering that modern medicinal chemistry emerged in the early 20th century from the synthetic dye industry of the late 19th century (mostly in Germany at that time) (Paterson, 1984). Following the discovery of the first synthetic dye in 1856, Paul Ehrlich (1854–1915) (Drews, 2004; Bosch and Rosich, 2008), who acquired his medical doctor’s degree with a thesis on “the theory and practice of histological staining”, laid the foundations of chemotherapy. The analogy between the azo –N=N– bond common in many of these dyes and the arsenic bond –As=As– led to his search of arsenicals and ultimately to the discovery of arsphenamine (Salvarsan, no. 606), the first modern antimicrobial, in 1909. A few years later, the testing of thousands of azo dye related compounds and the contributions of Gerhard Domagk (1895–1964) led to the discovery of Prontosil (1932), the first effective sulfonamide antibacterial.
FIGURE 6. Illustrative selectivity plot comparing inhibitory activity of SMIs against two PPIs. Selectivity plot showing the inhibitory activity of some of the compounds found to inhibit the SARS-CoV-2-S-RBD–hACE2 as the targeted PPI (quantified as log IC50) versus that against another non-targeted PPI (here, TNF-R1–TNF-α PPI). More active and selective compounds are clustered toward the lower right corner. Figure prepared with data from (Bojadzic et al., 2021b).
None of the SMIs of SARS-CoV-2-S–hACE2 identified so far and discussed here (Figure 5) have reached clinical development (Zhao et al., 2022); in fact, none seem to have even been evaluated in existing preclinical animal models for SARS-CoV-2 (Takayama, 2020; Saravanan et al., 2022). Methylene blue, a phenothiazine dye we have identified as such an SMI (Bojadzic et al., 2021a), is, in fact, included in the WHO List of Essential Medicines and is orally bioactive; thus it might have some potential for repositioning for COVID-19 prevention and treatment especially as its low micromolar anti-CoV activity, possibly due to multiple mechanisms of action, has been confirmed by several other groups (Chuang et al., 2022). Overall, results summarized here provide proof-of-principle evidence for the feasibility of such SMI approaches toward antivirals that inhibit CoV attachment and entry, and they serve as a first guide of the chemical space needed to achieve this.
Author Contributions
PB is the sole author; he conceived and wrote the manuscript.
Conflict of Interest
The author declares the following competing financial interest(s): The University of Miami has filed a patent on some of the DRI-C compounds discussed here and their use for potential antiviral applications with PB as inventor.
Publisher’s Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Acknowledgments
The author is grateful to people in his lab (Oscar Alcazar, Damir Bojadzic, and Sung-Ting Chuang) for their dedicated work on this and other projects despite the challenges imposed by the COVID-19 pandemic and the related restrictions and lockdowns.
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Keywords: antiviral, coronavirus, fostemsavir, methylene blue, protein-protein interaction, SARS-cov-2, spike protein, variants of concern
Citation: Buchwald P (2022) Developing Small-Molecule Inhibitors of Protein-Protein Interactions Involved in Viral Entry as Potential Antivirals for COVID-19. Front. Drug. Discov. 2:898035. doi: 10.3389/fddsv.2022.898035
Received: 16 March 2022; Accepted: 31 March 2022;
Published: 25 April 2022.
Edited by:
Bruno Villoutreix, Institut National de la Santé et de la Recherche Médicale (INSERM), FranceReviewed by:
Daniela Trisciuzzi, University of Bari Aldo Moro, ItalyPhillippe Roche, Cancer Research Center of Marseille/CNRS, France
Copyright © 2022 Buchwald. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Peter Buchwald, pbuchwald@med.miami.edu