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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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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
1997
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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. |
format | Text |
id | pubmed-2233784 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1997 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
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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