AUTHOR=Soussia Ismail Ben , Choveau Frank S. , Blin Sandy , Kim Eun-Jin , Feliciangeli Sylvain , Chatelain Franck C. , Kang Dawon , Bichet Delphine , Lesage Florian 

TITLE=Antagonistic Effect of a Cytoplasmic Domain on the Basal Activity of Polymodal Potassium Channels

JOURNAL=Frontiers in Molecular Neuroscience

VOLUME=11

YEAR=2018

URL=https://www.frontiersin.org/journals/molecular-neuroscience/articles/10.3389/fnmol.2018.00301

DOI=10.3389/fnmol.2018.00301

ISSN=1662-5099

ABSTRACT=<p>TREK/TRAAK channels are polymodal K<sup>+</sup> channels that convert very diverse stimuli, including bioactive lipids, mechanical stretch and temperature, into electrical signals. The nature of the structural changes that regulate their activity remains an open question. Here, we show that a cytoplasmic domain (the proximal C-ter domain, pCt) exerts antagonistic effects in TREK1 and TRAAK. In basal conditions, pCt favors activity in TREK1 whereas it impairs TRAAK activity. Using the conformation-dependent binding of fluoxetine, we show that TREK1 and TRAAK conformations at rest are different, and under the influence of pCt. Finally, we show that depleting PIP<sub>2</sub> in live cells has a more pronounced inhibitory effect on TREK1 than on TRAAK. This differential regulation of TREK1 and TRAAK is related to a previously unrecognized PIP<sub>2</sub>-binding site (R329, R330, and R331) present within TREK1 pCt, but not in TRAAK pCt. Collectively, these new data point out pCt as a major regulatory domain of these channels and suggest that the binding of PIP<sub>2</sub> to the pCt of TREK1 results in the stabilization of the conductive conformation in basal conditions.</p>