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A Direct Demonstration of Closed-State Inactivation of K(+) Channels at Low pH
Lowering external pH reduces peak current and enhances current decay in Kv and Shaker-IR channels. Using voltage-clamp fluorimetry we directly determined the fate of Shaker-IR channels at low pH by measuring fluorescence emission from tetramethylrhodamine-5-maleimide attached to substituted cysteine...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2154379/ https://www.ncbi.nlm.nih.gov/pubmed/17470663 http://dx.doi.org/10.1085/jgp.200709774 |
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author | Claydon, Thomas W. Vaid, Moni Rezazadeh, Saman Kwan, Daniel C.H. Kehl, Steven J. Fedida, David |
author_facet | Claydon, Thomas W. Vaid, Moni Rezazadeh, Saman Kwan, Daniel C.H. Kehl, Steven J. Fedida, David |
author_sort | Claydon, Thomas W. |
collection | PubMed |
description | Lowering external pH reduces peak current and enhances current decay in Kv and Shaker-IR channels. Using voltage-clamp fluorimetry we directly determined the fate of Shaker-IR channels at low pH by measuring fluorescence emission from tetramethylrhodamine-5-maleimide attached to substituted cysteine residues in the voltage sensor domain (M356C to R362C) or S5-P linker (S424C). One aspect of the distal S3-S4 linker α-helix (A359C and R362C) reported a pH-induced acceleration of the slow phase of fluorescence quenching that represents P/C-type inactivation, but neither site reported a change in the total charge movement at low pH. Shaker S424C fluorescence demonstrated slow unquenching that also reflects channel inactivation and this too was accelerated at low pH. In addition, however, acidic pH caused a reversible loss of the fluorescence signal (pKa = 5.1) that paralleled the reduction of peak current amplitude (pKa = 5.2). Protons decreased single channel open probability, suggesting that the loss of fluorescence at low pH reflects a decreased channel availability that is responsible for the reduced macroscopic conductance. Inhibition of inactivation in Shaker S424C (by raising external K(+) or the mutation T449V) prevented fluorescence loss at low pH, and the fluorescence report from closed Shaker ILT S424C channels implied that protons stabilized a W434F-like inactivated state. Furthermore, acidic pH changed the fluorescence amplitude (pKa = 5.9) in channels held continuously at −80 mV. This suggests that low pH stabilizes closed-inactivated states. Thus, fluorescence experiments suggest the major mechanism of pH-induced peak current reduction is inactivation of channels from closed states from which they can activate, but not open; this occurs in addition to acceleration of P/C-type inactivation from the open state. |
format | Text |
id | pubmed-2154379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21543792008-01-17 A Direct Demonstration of Closed-State Inactivation of K(+) Channels at Low pH Claydon, Thomas W. Vaid, Moni Rezazadeh, Saman Kwan, Daniel C.H. Kehl, Steven J. Fedida, David J Gen Physiol Articles Lowering external pH reduces peak current and enhances current decay in Kv and Shaker-IR channels. Using voltage-clamp fluorimetry we directly determined the fate of Shaker-IR channels at low pH by measuring fluorescence emission from tetramethylrhodamine-5-maleimide attached to substituted cysteine residues in the voltage sensor domain (M356C to R362C) or S5-P linker (S424C). One aspect of the distal S3-S4 linker α-helix (A359C and R362C) reported a pH-induced acceleration of the slow phase of fluorescence quenching that represents P/C-type inactivation, but neither site reported a change in the total charge movement at low pH. Shaker S424C fluorescence demonstrated slow unquenching that also reflects channel inactivation and this too was accelerated at low pH. In addition, however, acidic pH caused a reversible loss of the fluorescence signal (pKa = 5.1) that paralleled the reduction of peak current amplitude (pKa = 5.2). Protons decreased single channel open probability, suggesting that the loss of fluorescence at low pH reflects a decreased channel availability that is responsible for the reduced macroscopic conductance. Inhibition of inactivation in Shaker S424C (by raising external K(+) or the mutation T449V) prevented fluorescence loss at low pH, and the fluorescence report from closed Shaker ILT S424C channels implied that protons stabilized a W434F-like inactivated state. Furthermore, acidic pH changed the fluorescence amplitude (pKa = 5.9) in channels held continuously at −80 mV. This suggests that low pH stabilizes closed-inactivated states. Thus, fluorescence experiments suggest the major mechanism of pH-induced peak current reduction is inactivation of channels from closed states from which they can activate, but not open; this occurs in addition to acceleration of P/C-type inactivation from the open state. The Rockefeller University Press 2007-05 /pmc/articles/PMC2154379/ /pubmed/17470663 http://dx.doi.org/10.1085/jgp.200709774 Text en Copyright © 2007, 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 Claydon, Thomas W. Vaid, Moni Rezazadeh, Saman Kwan, Daniel C.H. Kehl, Steven J. Fedida, David A Direct Demonstration of Closed-State Inactivation of K(+) Channels at Low pH |
title | A Direct Demonstration of Closed-State Inactivation of K(+) Channels at Low pH |
title_full | A Direct Demonstration of Closed-State Inactivation of K(+) Channels at Low pH |
title_fullStr | A Direct Demonstration of Closed-State Inactivation of K(+) Channels at Low pH |
title_full_unstemmed | A Direct Demonstration of Closed-State Inactivation of K(+) Channels at Low pH |
title_short | A Direct Demonstration of Closed-State Inactivation of K(+) Channels at Low pH |
title_sort | direct demonstration of closed-state inactivation of k(+) channels at low ph |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2154379/ https://www.ncbi.nlm.nih.gov/pubmed/17470663 http://dx.doi.org/10.1085/jgp.200709774 |
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