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Modulation of Pore Opening of Eukaryotic Sodium Channels by π-Helices in S6

[Image: see text] Voltage-gated sodium channels are heterotetrameric sodium selective ion channels that play a central role in electrical signaling in excitable cells. With recent advances in structural biology, structures of eukaryotic sodium channels have been captured in several distinct conforma...

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Autores principales: Choudhury, Koushik, Delemotte, Lucie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316397/
https://www.ncbi.nlm.nih.gov/pubmed/37341700
http://dx.doi.org/10.1021/acs.jpclett.3c00803
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author Choudhury, Koushik
Delemotte, Lucie
author_facet Choudhury, Koushik
Delemotte, Lucie
author_sort Choudhury, Koushik
collection PubMed
description [Image: see text] Voltage-gated sodium channels are heterotetrameric sodium selective ion channels that play a central role in electrical signaling in excitable cells. With recent advances in structural biology, structures of eukaryotic sodium channels have been captured in several distinct conformations corresponding to different functional states. The secondary structure of the pore lining S6 helices of subunits DI, DII, and DIV has been captured with both short π-helix stretches and in fully α-helical conformations. The relevance of these secondary structure elements for pore gating is not yet understood. Here, we propose that a π-helix in at least DI-S6, DIII-S6, and DIV-S6 results in a fully conductive state. On the other hand, the absence of π-helix in either DI-S6 or DIV-S6 yields a subconductance state, and its absence from both DI-S6 and DIV-S6 yields a nonconducting state. This work highlights the impact of the presence of a π-helix in the different S6 helices of an expanded pore on pore conductance, thus opening new doors toward reconstructing the entire conformational landscape along the functional cycle of Nav Channels and paving the way to the design of state-dependent modulators.
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spelling pubmed-103163972023-07-04 Modulation of Pore Opening of Eukaryotic Sodium Channels by π-Helices in S6 Choudhury, Koushik Delemotte, Lucie J Phys Chem Lett [Image: see text] Voltage-gated sodium channels are heterotetrameric sodium selective ion channels that play a central role in electrical signaling in excitable cells. With recent advances in structural biology, structures of eukaryotic sodium channels have been captured in several distinct conformations corresponding to different functional states. The secondary structure of the pore lining S6 helices of subunits DI, DII, and DIV has been captured with both short π-helix stretches and in fully α-helical conformations. The relevance of these secondary structure elements for pore gating is not yet understood. Here, we propose that a π-helix in at least DI-S6, DIII-S6, and DIV-S6 results in a fully conductive state. On the other hand, the absence of π-helix in either DI-S6 or DIV-S6 yields a subconductance state, and its absence from both DI-S6 and DIV-S6 yields a nonconducting state. This work highlights the impact of the presence of a π-helix in the different S6 helices of an expanded pore on pore conductance, thus opening new doors toward reconstructing the entire conformational landscape along the functional cycle of Nav Channels and paving the way to the design of state-dependent modulators. American Chemical Society 2023-06-21 /pmc/articles/PMC10316397/ /pubmed/37341700 http://dx.doi.org/10.1021/acs.jpclett.3c00803 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Choudhury, Koushik
Delemotte, Lucie
Modulation of Pore Opening of Eukaryotic Sodium Channels by π-Helices in S6
title Modulation of Pore Opening of Eukaryotic Sodium Channels by π-Helices in S6
title_full Modulation of Pore Opening of Eukaryotic Sodium Channels by π-Helices in S6
title_fullStr Modulation of Pore Opening of Eukaryotic Sodium Channels by π-Helices in S6
title_full_unstemmed Modulation of Pore Opening of Eukaryotic Sodium Channels by π-Helices in S6
title_short Modulation of Pore Opening of Eukaryotic Sodium Channels by π-Helices in S6
title_sort modulation of pore opening of eukaryotic sodium channels by π-helices in s6
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316397/
https://www.ncbi.nlm.nih.gov/pubmed/37341700
http://dx.doi.org/10.1021/acs.jpclett.3c00803
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