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The nonconducting W434F mutant adopts upon membrane depolarization an inactivated-like state that differs from wild-type Shaker-IR potassium channels

Voltage-gated K(+) (Kv) channels mediate the flow of K(+) across the cell membrane by regulating the conductive state of their activation gate (AG). Several Kv channels display slow C-type inactivation, a process whereby their selectivity filter (SF) becomes less or nonconductive. It has been propos...

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Autores principales: Coonen, Laura, Martinez-Morales, Evelyn, Van De Sande, Dieter V., Snyders, Dirk J., Cortes, D. Marien, Cuello, Luis G., Labro, Alain J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9481120/
https://www.ncbi.nlm.nih.gov/pubmed/36112676
http://dx.doi.org/10.1126/sciadv.abn1731
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author Coonen, Laura
Martinez-Morales, Evelyn
Van De Sande, Dieter V.
Snyders, Dirk J.
Cortes, D. Marien
Cuello, Luis G.
Labro, Alain J.
author_facet Coonen, Laura
Martinez-Morales, Evelyn
Van De Sande, Dieter V.
Snyders, Dirk J.
Cortes, D. Marien
Cuello, Luis G.
Labro, Alain J.
author_sort Coonen, Laura
collection PubMed
description Voltage-gated K(+) (Kv) channels mediate the flow of K(+) across the cell membrane by regulating the conductive state of their activation gate (AG). Several Kv channels display slow C-type inactivation, a process whereby their selectivity filter (SF) becomes less or nonconductive. It has been proposed that, in the fast inactivation-removed Shaker-IR channel, the W434F mutation epitomizes the C-type inactivated state because it functionally accelerates this process. By introducing another pore mutation that prevents AG closure, P475D, we found a way to record ionic currents of the Shaker-IR-W434F-P475D mutant at hyperpolarized membrane potentials as the W434F-mutant SF recovers from its inactivated state. This W434F conductive state lost its high K(+) over Na(+) selectivity, and even NMDG(+) can permeate, features not observed in a wild-type SF. This indicates that, at least during recovery from inactivation, the W434F-mutant SF transitions to a widened and noncationic specific conformation.
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spelling pubmed-94811202022-09-29 The nonconducting W434F mutant adopts upon membrane depolarization an inactivated-like state that differs from wild-type Shaker-IR potassium channels Coonen, Laura Martinez-Morales, Evelyn Van De Sande, Dieter V. Snyders, Dirk J. Cortes, D. Marien Cuello, Luis G. Labro, Alain J. Sci Adv Biomedicine and Life Sciences Voltage-gated K(+) (Kv) channels mediate the flow of K(+) across the cell membrane by regulating the conductive state of their activation gate (AG). Several Kv channels display slow C-type inactivation, a process whereby their selectivity filter (SF) becomes less or nonconductive. It has been proposed that, in the fast inactivation-removed Shaker-IR channel, the W434F mutation epitomizes the C-type inactivated state because it functionally accelerates this process. By introducing another pore mutation that prevents AG closure, P475D, we found a way to record ionic currents of the Shaker-IR-W434F-P475D mutant at hyperpolarized membrane potentials as the W434F-mutant SF recovers from its inactivated state. This W434F conductive state lost its high K(+) over Na(+) selectivity, and even NMDG(+) can permeate, features not observed in a wild-type SF. This indicates that, at least during recovery from inactivation, the W434F-mutant SF transitions to a widened and noncationic specific conformation. American Association for the Advancement of Science 2022-09-16 /pmc/articles/PMC9481120/ /pubmed/36112676 http://dx.doi.org/10.1126/sciadv.abn1731 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Biomedicine and Life Sciences
Coonen, Laura
Martinez-Morales, Evelyn
Van De Sande, Dieter V.
Snyders, Dirk J.
Cortes, D. Marien
Cuello, Luis G.
Labro, Alain J.
The nonconducting W434F mutant adopts upon membrane depolarization an inactivated-like state that differs from wild-type Shaker-IR potassium channels
title The nonconducting W434F mutant adopts upon membrane depolarization an inactivated-like state that differs from wild-type Shaker-IR potassium channels
title_full The nonconducting W434F mutant adopts upon membrane depolarization an inactivated-like state that differs from wild-type Shaker-IR potassium channels
title_fullStr The nonconducting W434F mutant adopts upon membrane depolarization an inactivated-like state that differs from wild-type Shaker-IR potassium channels
title_full_unstemmed The nonconducting W434F mutant adopts upon membrane depolarization an inactivated-like state that differs from wild-type Shaker-IR potassium channels
title_short The nonconducting W434F mutant adopts upon membrane depolarization an inactivated-like state that differs from wild-type Shaker-IR potassium channels
title_sort nonconducting w434f mutant adopts upon membrane depolarization an inactivated-like state that differs from wild-type shaker-ir potassium channels
topic Biomedicine and Life Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9481120/
https://www.ncbi.nlm.nih.gov/pubmed/36112676
http://dx.doi.org/10.1126/sciadv.abn1731
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