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The Cooperative Voltage Sensor Motion that Gates a Potassium Channel
The four arginine-rich S4 helices of a voltage-gated channel move outward through the membrane in response to depolarization, opening and closing gates to generate a transient ionic current. Coupling of voltage sensing to gating was originally thought to operate with the S4s moving independently fro...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1414780/ https://www.ncbi.nlm.nih.gov/pubmed/15623895 http://dx.doi.org/10.1085/jgp.200409197 |
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author | Pathak, Medha Kurtz, Lisa Tombola, Francesco Isacoff, Ehud |
author_facet | Pathak, Medha Kurtz, Lisa Tombola, Francesco Isacoff, Ehud |
author_sort | Pathak, Medha |
collection | PubMed |
description | The four arginine-rich S4 helices of a voltage-gated channel move outward through the membrane in response to depolarization, opening and closing gates to generate a transient ionic current. Coupling of voltage sensing to gating was originally thought to operate with the S4s moving independently from an inward/resting to an outward/activated conformation, so that when all four S4s are activated, the gates are driven to open or closed. However, S4 has also been found to influence the cooperative opening step (Smith-Maxwell et al., 1998a), suggesting a more complex mechanism of coupling. Using fluorescence to monitor structural rearrangements in a Shaker channel mutant, the ILT channel (Ledwell and Aldrich, 1999), that energetically isolates the steps of activation from the cooperative opening step, we find that opening is accompanied by a previously unknown and cooperative movement of S4. This gating motion of S4 appears to be coupled to the internal S6 gate and to two forms of slow inactivation. Our results suggest that S4 plays a direct role in gating. While large transmembrane rearrangements of S4 may be required to unlock the gating machinery, as proposed before, it appears to be the gating motion of S4 that drives the gates to open and close. |
format | Text |
id | pubmed-1414780 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-14147802008-03-21 The Cooperative Voltage Sensor Motion that Gates a Potassium Channel Pathak, Medha Kurtz, Lisa Tombola, Francesco Isacoff, Ehud J Gen Physiol Article The four arginine-rich S4 helices of a voltage-gated channel move outward through the membrane in response to depolarization, opening and closing gates to generate a transient ionic current. Coupling of voltage sensing to gating was originally thought to operate with the S4s moving independently from an inward/resting to an outward/activated conformation, so that when all four S4s are activated, the gates are driven to open or closed. However, S4 has also been found to influence the cooperative opening step (Smith-Maxwell et al., 1998a), suggesting a more complex mechanism of coupling. Using fluorescence to monitor structural rearrangements in a Shaker channel mutant, the ILT channel (Ledwell and Aldrich, 1999), that energetically isolates the steps of activation from the cooperative opening step, we find that opening is accompanied by a previously unknown and cooperative movement of S4. This gating motion of S4 appears to be coupled to the internal S6 gate and to two forms of slow inactivation. Our results suggest that S4 plays a direct role in gating. While large transmembrane rearrangements of S4 may be required to unlock the gating machinery, as proposed before, it appears to be the gating motion of S4 that drives the gates to open and close. The Rockefeller University Press 2005-01 /pmc/articles/PMC1414780/ /pubmed/15623895 http://dx.doi.org/10.1085/jgp.200409197 Text en Copyright © 2005, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Article Pathak, Medha Kurtz, Lisa Tombola, Francesco Isacoff, Ehud The Cooperative Voltage Sensor Motion that Gates a Potassium Channel |
title | The Cooperative Voltage Sensor Motion that Gates a Potassium Channel |
title_full | The Cooperative Voltage Sensor Motion that Gates a Potassium Channel |
title_fullStr | The Cooperative Voltage Sensor Motion that Gates a Potassium Channel |
title_full_unstemmed | The Cooperative Voltage Sensor Motion that Gates a Potassium Channel |
title_short | The Cooperative Voltage Sensor Motion that Gates a Potassium Channel |
title_sort | cooperative voltage sensor motion that gates a potassium channel |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1414780/ https://www.ncbi.nlm.nih.gov/pubmed/15623895 http://dx.doi.org/10.1085/jgp.200409197 |
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