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Temperature Dependence of Fast and Slow Gating Relaxations of ClC-0 Chloride Channels

The chloride channel from the Torpedo electric organ, ClC-0, is the best studied member of a large gene-family (Jentsch, T.J. 1996. Curr. Opin. Neurobiol. 6:303–310.). We investigate the temperature dependence of both the voltage- and chloride-dependent fast gate and of the slow gate of the “double-...

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Autores principales: Pusch, Michael, Ludewig, Uwe, Jentsch, Thomas J.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2217054/
https://www.ncbi.nlm.nih.gov/pubmed/8997669
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author Pusch, Michael
Ludewig, Uwe
Jentsch, Thomas J.
author_facet Pusch, Michael
Ludewig, Uwe
Jentsch, Thomas J.
author_sort Pusch, Michael
collection PubMed
description The chloride channel from the Torpedo electric organ, ClC-0, is the best studied member of a large gene-family (Jentsch, T.J. 1996. Curr. Opin. Neurobiol. 6:303–310.). We investigate the temperature dependence of both the voltage- and chloride-dependent fast gate and of the slow gate of the “double-barreled” ClC-0 expressed in Xenopus oocytes. Kinetics of the fast gate exhibit only a moderate temperature dependence with a Q(10) of 2.2. Steady-state p (open) of the fast gate is relatively independent of temperature. The slow gate, in contrast, is highly temperature sensitive. Deactivation kinetics at positive voltages are associated with a Q(10) of ∼40. Steady-state open probability of the slow gate (p (open) (slow)(V)) can be described by a Boltzmann distribution with an apparent gating valence of ≈2 and a variable “offset” at positive voltages. We note a positive correlation of this offset (i.e., the fraction of channels that are not closed by the slow gate) with the amount of expression. This offset is also highly temperature sensitive, being drastically decreased at high temperatures. Paradoxically, the maximum degree of activation of the slow gate also decreases at higher temperatures. The strong temperature dependence of the slow gate was also observed at the single channel level in inside-out patches. The results imply that within a Markovian-type description at least two open and two closed states are needed to describe slow gating. The strong temperature dependence of the slow gate explains the phenotype of several ClC-0 point-mutants described recently by Ludewig et al. (Ludewig, U., T.J. Jentsch, and M. Pusch. 1996. J. Physiol. (Lond.). In press). The large Q(10) of slow gating kinetics points to a complex rearrangement. This, together with the correlation of the fraction of noninactivating channels with the amount of expression and the fact that the slow gate closes both protochannels simultaneously suggests that the slow gate is coupled to subunit interaction of the multimeric ClC-0 channel.
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spelling pubmed-22170542008-04-22 Temperature Dependence of Fast and Slow Gating Relaxations of ClC-0 Chloride Channels Pusch, Michael Ludewig, Uwe Jentsch, Thomas J. J Gen Physiol Article The chloride channel from the Torpedo electric organ, ClC-0, is the best studied member of a large gene-family (Jentsch, T.J. 1996. Curr. Opin. Neurobiol. 6:303–310.). We investigate the temperature dependence of both the voltage- and chloride-dependent fast gate and of the slow gate of the “double-barreled” ClC-0 expressed in Xenopus oocytes. Kinetics of the fast gate exhibit only a moderate temperature dependence with a Q(10) of 2.2. Steady-state p (open) of the fast gate is relatively independent of temperature. The slow gate, in contrast, is highly temperature sensitive. Deactivation kinetics at positive voltages are associated with a Q(10) of ∼40. Steady-state open probability of the slow gate (p (open) (slow)(V)) can be described by a Boltzmann distribution with an apparent gating valence of ≈2 and a variable “offset” at positive voltages. We note a positive correlation of this offset (i.e., the fraction of channels that are not closed by the slow gate) with the amount of expression. This offset is also highly temperature sensitive, being drastically decreased at high temperatures. Paradoxically, the maximum degree of activation of the slow gate also decreases at higher temperatures. The strong temperature dependence of the slow gate was also observed at the single channel level in inside-out patches. The results imply that within a Markovian-type description at least two open and two closed states are needed to describe slow gating. The strong temperature dependence of the slow gate explains the phenotype of several ClC-0 point-mutants described recently by Ludewig et al. (Ludewig, U., T.J. Jentsch, and M. Pusch. 1996. J. Physiol. (Lond.). In press). The large Q(10) of slow gating kinetics points to a complex rearrangement. This, together with the correlation of the fraction of noninactivating channels with the amount of expression and the fact that the slow gate closes both protochannels simultaneously suggests that the slow gate is coupled to subunit interaction of the multimeric ClC-0 channel. The Rockefeller University Press 1997-01-01 /pmc/articles/PMC2217054/ /pubmed/8997669 Text en 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
Pusch, Michael
Ludewig, Uwe
Jentsch, Thomas J.
Temperature Dependence of Fast and Slow Gating Relaxations of ClC-0 Chloride Channels
title Temperature Dependence of Fast and Slow Gating Relaxations of ClC-0 Chloride Channels
title_full Temperature Dependence of Fast and Slow Gating Relaxations of ClC-0 Chloride Channels
title_fullStr Temperature Dependence of Fast and Slow Gating Relaxations of ClC-0 Chloride Channels
title_full_unstemmed Temperature Dependence of Fast and Slow Gating Relaxations of ClC-0 Chloride Channels
title_short Temperature Dependence of Fast and Slow Gating Relaxations of ClC-0 Chloride Channels
title_sort temperature dependence of fast and slow gating relaxations of clc-0 chloride channels
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2217054/
https://www.ncbi.nlm.nih.gov/pubmed/8997669
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