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Inward Rectification in ClC-0 Chloride Channels Caused by Mutations in Several Protein Regions

Several cloned ClC-type Cl(−) channels open and close in a voltage-dependent manner. The Torpedo electric organ Cl(−) channel, ClC-0, is the best studied member of this gene family. ClC-0 is gated by a fast and a slow gating mechanism of opposite voltage direction. Fast gating is dependent on voltag...

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Autores principales: Ludewig, Uwe, Jentsch, Thomas J., Pusch, Michael
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2233784/
https://www.ncbi.nlm.nih.gov/pubmed/9236209
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author Ludewig, Uwe
Jentsch, Thomas J.
Pusch, Michael
author_facet Ludewig, Uwe
Jentsch, Thomas J.
Pusch, Michael
author_sort Ludewig, Uwe
collection PubMed
description Several cloned ClC-type Cl(−) channels open and close in a voltage-dependent manner. The Torpedo electric organ Cl(−) channel, ClC-0, is the best studied member of this gene family. ClC-0 is gated by a fast and a slow gating mechanism of opposite voltage direction. Fast gating is dependent on voltage and on the external and internal Cl(−) concentration, and it has been proposed that the permeant anion serves as the gating charge in ClC-0 (Pusch, M., U. Ludewig, A. Rehfeldt, and T.J. Jentsch. 1995. Nature (Lond.). 373:527–531). The deactivation at negative voltages of the muscular ClC-1 channel is similar but not identical to ClC-0. Different from the extrinsic voltage dependence suggested for ClC-0, an intrinsic voltage sensor had been proposed to underlie the voltage dependence in ClC-1 (Fahlke, C., R. Rüdel, N. Mitrovic, M. Zhou, and A.L. George. 1995. Neuron. 15:463–472; Fahlke, C., A. Rosenbohm, N. Mitrovic, A.L. George, and R. Rüdel. 1996. Biophys. J. 71:695–706). The gating model for ClC-1 was partially based on the properties of a point-mutation found in recessice myotonia (D136G). Here we investigate the functional effects of mutating the corresponding residue in ClC-0 (D70). Both the corresponding charge neutralization (D70G) and a charge conserving mutation (D70E) led to an inwardly rectifying phenotype resembling that of ClC-1 (D136G). Several other mutations at very different positions in ClC-0 (K165R, H472K, S475T, E482D, T484S, T484Q), however, also led to a similar phenotype. In one of these mutants (T484S) the typical wild-type gating, characterized by a deactivation at negative voltages, can be partially restored by using external perchlorate (ClO(4) (−)) solutions. We conclude that gating in ClC-0 and ClC-1 is due to similar mechanisms. The negative charge at position 70 in ClC-0 does not specifically confer the voltage sensitivity in ClC-channels, and there is no need to postulate an intrinsic voltage sensor in ClC-channels.
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spelling pubmed-22337842008-04-22 Inward Rectification in ClC-0 Chloride Channels Caused by Mutations in Several Protein Regions Ludewig, Uwe Jentsch, Thomas J. Pusch, Michael J Gen Physiol Article Several cloned ClC-type Cl(−) channels open and close in a voltage-dependent manner. The Torpedo electric organ Cl(−) channel, ClC-0, is the best studied member of this gene family. ClC-0 is gated by a fast and a slow gating mechanism of opposite voltage direction. Fast gating is dependent on voltage and on the external and internal Cl(−) concentration, and it has been proposed that the permeant anion serves as the gating charge in ClC-0 (Pusch, M., U. Ludewig, A. Rehfeldt, and T.J. Jentsch. 1995. Nature (Lond.). 373:527–531). The deactivation at negative voltages of the muscular ClC-1 channel is similar but not identical to ClC-0. Different from the extrinsic voltage dependence suggested for ClC-0, an intrinsic voltage sensor had been proposed to underlie the voltage dependence in ClC-1 (Fahlke, C., R. Rüdel, N. Mitrovic, M. Zhou, and A.L. George. 1995. Neuron. 15:463–472; Fahlke, C., A. Rosenbohm, N. Mitrovic, A.L. George, and R. Rüdel. 1996. Biophys. J. 71:695–706). The gating model for ClC-1 was partially based on the properties of a point-mutation found in recessice myotonia (D136G). Here we investigate the functional effects of mutating the corresponding residue in ClC-0 (D70). Both the corresponding charge neutralization (D70G) and a charge conserving mutation (D70E) led to an inwardly rectifying phenotype resembling that of ClC-1 (D136G). Several other mutations at very different positions in ClC-0 (K165R, H472K, S475T, E482D, T484S, T484Q), however, also led to a similar phenotype. In one of these mutants (T484S) the typical wild-type gating, characterized by a deactivation at negative voltages, can be partially restored by using external perchlorate (ClO(4) (−)) solutions. We conclude that gating in ClC-0 and ClC-1 is due to similar mechanisms. The negative charge at position 70 in ClC-0 does not specifically confer the voltage sensitivity in ClC-channels, and there is no need to postulate an intrinsic voltage sensor in ClC-channels. The Rockefeller University Press 1997-08-01 /pmc/articles/PMC2233784/ /pubmed/9236209 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
Ludewig, Uwe
Jentsch, Thomas J.
Pusch, Michael
Inward Rectification in ClC-0 Chloride Channels Caused by Mutations in Several Protein Regions
title Inward Rectification in ClC-0 Chloride Channels Caused by Mutations in Several Protein Regions
title_full Inward Rectification in ClC-0 Chloride Channels Caused by Mutations in Several Protein Regions
title_fullStr Inward Rectification in ClC-0 Chloride Channels Caused by Mutations in Several Protein Regions
title_full_unstemmed Inward Rectification in ClC-0 Chloride Channels Caused by Mutations in Several Protein Regions
title_short Inward Rectification in ClC-0 Chloride Channels Caused by Mutations in Several Protein Regions
title_sort inward rectification in clc-0 chloride channels caused by mutations in several protein regions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2233784/
https://www.ncbi.nlm.nih.gov/pubmed/9236209
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