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The plasma membrane inner leaflet PI(4,5)P2 is essential for the activation of proton-activated chloride channels

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dc.contributor.authorKo, Woori-
dc.contributor.authorLee, Euna-
dc.contributor.authorKim, Jung-Eun-
dc.contributor.authorLim, Hyun-Ho-
dc.contributor.authorSuh, Byung-Chang-
dc.date.accessioned2024-08-22T00:30:13Z-
dc.date.available2024-08-22T00:30:13Z-
dc.date.issued2024-08-
dc.identifier.issn2041-1723-
dc.identifier.urihttp://scholarworks.bwise.kr/kbri/handle/2023.sw.kbri/1190-
dc.description.abstractProton-activated chloride (PAC) channels, ubiquitously expressed in tissues, regulate intracellular Cl- levels and cell death following acidosis. However, molecular mechanisms and signaling pathways involved in PAC channel modulation are largely unknown. Herein, we determine that phosphatidylinositol 4,5-bisphosphate [PI(4,5)P-2] of the plasma membrane inner leaflet is essential for the proton activation of PAC channels. PI(4,5)P-2 depletion by activating phosphatidylinositol 5-phosphatases or G(q) protein-coupled muscarinic receptors substantially inhibits human PAC currents. In excised inside-out patches, PI(4,5)P-2 application to the cytoplasmic side increases the currents. Structural simulation reveals that the putative PI(4,5)P-2-binding site is localized within the cytosol in resting state but shifts to the cell membrane's inner surface in an activated state and interacts with inner leaflet PI(4,5)P-2. Alanine neutralization of basic residues near the membrane-cytosol interface of the transmembrane helice 2 significantly attenuates PAC currents. Overall, our study uncovers a modulatory mechanism of PAC channel through inner membrane PI(4,5)P-2.-
dc.publisherNature Publishing Group-
dc.titleThe plasma membrane inner leaflet PI(4,5)P2 is essential for the activation of proton-activated chloride channels-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1038/s41467-024-51400-y-
dc.identifier.wosid001291855700002-
dc.identifier.bibliographicCitationNature Communications, v.15, no.1-
dc.citation.titleNature Communications-
dc.citation.volume15-
dc.citation.number1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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연구본부 (신경·혈관단위체 연구그룹)
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