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A Trapped Intracellular Cation Modulates K(+) Channel Recovery From Slow Inactivation

Upon depolarization, many voltage-gated potassium channels undergo a time-dependent decrease in conductance known as inactivation. Both entry of channels into an inactivated state and recovery from this state govern cellular excitability. In this study, we show that recovery from slow inactivation i...

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Detalles Bibliográficos
Autores principales: Ray, Evan C., Deutsch, Carol
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2151525/
https://www.ncbi.nlm.nih.gov/pubmed/16847099
http://dx.doi.org/10.1085/jgp.200609561
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author Ray, Evan C.
Deutsch, Carol
author_facet Ray, Evan C.
Deutsch, Carol
author_sort Ray, Evan C.
collection PubMed
description Upon depolarization, many voltage-gated potassium channels undergo a time-dependent decrease in conductance known as inactivation. Both entry of channels into an inactivated state and recovery from this state govern cellular excitability. In this study, we show that recovery from slow inactivation is regulated by intracellular permeant cations. When inactivated channels are hyperpolarized, closure of the activation gate traps a cation between the activation and inactivation gates. The identity of the trapped cation determines the rate of recovery, and the ability of cations to promote recovery follows the rank order K(+) > NH(4) (+) > Rb(+) > Cs(+) >> Na(+), TMA. The striking similarity between this rank order and that for single channel conductance suggests that these two processes share a common feature. We propose that the rate of recovery from slow inactivation is determined by the ability of entrapped cations to move into a binding site in the channel's selectivity filter, and refilling of this site is required for recovery.
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spelling pubmed-21515252008-01-17 A Trapped Intracellular Cation Modulates K(+) Channel Recovery From Slow Inactivation Ray, Evan C. Deutsch, Carol J Gen Physiol Articles Upon depolarization, many voltage-gated potassium channels undergo a time-dependent decrease in conductance known as inactivation. Both entry of channels into an inactivated state and recovery from this state govern cellular excitability. In this study, we show that recovery from slow inactivation is regulated by intracellular permeant cations. When inactivated channels are hyperpolarized, closure of the activation gate traps a cation between the activation and inactivation gates. The identity of the trapped cation determines the rate of recovery, and the ability of cations to promote recovery follows the rank order K(+) > NH(4) (+) > Rb(+) > Cs(+) >> Na(+), TMA. The striking similarity between this rank order and that for single channel conductance suggests that these two processes share a common feature. We propose that the rate of recovery from slow inactivation is determined by the ability of entrapped cations to move into a binding site in the channel's selectivity filter, and refilling of this site is required for recovery. The Rockefeller University Press 2006-08 /pmc/articles/PMC2151525/ /pubmed/16847099 http://dx.doi.org/10.1085/jgp.200609561 Text en Copyright © 2006, 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 Articles
Ray, Evan C.
Deutsch, Carol
A Trapped Intracellular Cation Modulates K(+) Channel Recovery From Slow Inactivation
title A Trapped Intracellular Cation Modulates K(+) Channel Recovery From Slow Inactivation
title_full A Trapped Intracellular Cation Modulates K(+) Channel Recovery From Slow Inactivation
title_fullStr A Trapped Intracellular Cation Modulates K(+) Channel Recovery From Slow Inactivation
title_full_unstemmed A Trapped Intracellular Cation Modulates K(+) Channel Recovery From Slow Inactivation
title_short A Trapped Intracellular Cation Modulates K(+) Channel Recovery From Slow Inactivation
title_sort trapped intracellular cation modulates k(+) channel recovery from slow inactivation
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2151525/
https://www.ncbi.nlm.nih.gov/pubmed/16847099
http://dx.doi.org/10.1085/jgp.200609561
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