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The activation gate controls steady-state inactivation and recovery from inactivation in Shaker

Despite major advances in the structure determination of ion channels, the sequence of molecular rearrangements at negative membrane potentials in voltage-gated potassium channels of the Shaker family remains unknown. Four major composite gating states are documented during the gating process: close...

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Autores principales: Szanto, Tibor G., Zakany, Florina, Papp, Ferenc, Varga, Zoltan, Deutsch, Carol J., Panyi, Gyorgy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7398138/
https://www.ncbi.nlm.nih.gov/pubmed/32442242
http://dx.doi.org/10.1085/jgp.202012591
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author Szanto, Tibor G.
Zakany, Florina
Papp, Ferenc
Varga, Zoltan
Deutsch, Carol J.
Panyi, Gyorgy
author_facet Szanto, Tibor G.
Zakany, Florina
Papp, Ferenc
Varga, Zoltan
Deutsch, Carol J.
Panyi, Gyorgy
author_sort Szanto, Tibor G.
collection PubMed
description Despite major advances in the structure determination of ion channels, the sequence of molecular rearrangements at negative membrane potentials in voltage-gated potassium channels of the Shaker family remains unknown. Four major composite gating states are documented during the gating process: closed (C), open (O), open-inactivated (OI), and closed-inactivated (CI). Although many steps in the gating cycle have been clarified experimentally, the development of steady-state inactivation at negative membrane potentials and mandatory gating transitions for recovery from inactivation have not been elucidated. In this study, we exploit the biophysical properties of Shaker-IR mutants T449A/V474C and T449A/V476C to evaluate the status of the activation and inactivation gates during steady-state inactivation and upon locking the channel open with intracellular Cd(2+). We conclude that at negative membrane potentials, the gating scheme of Shaker channels can be refined in two aspects. First, the most likely pathway for the development of steady-state inactivation is C→O→OI [Formula: see text] CI. Second, the OI→CI transition is a prerequisite for recovery from inactivation. These findings are in accordance with the widely accepted view that tight coupling is present between the activation and C-type inactivation gates in Shaker and underscore the role of steady-state inactivation and recovery from inactivation as determinants of excitability.
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spelling pubmed-73981382021-02-03 The activation gate controls steady-state inactivation and recovery from inactivation in Shaker Szanto, Tibor G. Zakany, Florina Papp, Ferenc Varga, Zoltan Deutsch, Carol J. Panyi, Gyorgy J Gen Physiol Article Despite major advances in the structure determination of ion channels, the sequence of molecular rearrangements at negative membrane potentials in voltage-gated potassium channels of the Shaker family remains unknown. Four major composite gating states are documented during the gating process: closed (C), open (O), open-inactivated (OI), and closed-inactivated (CI). Although many steps in the gating cycle have been clarified experimentally, the development of steady-state inactivation at negative membrane potentials and mandatory gating transitions for recovery from inactivation have not been elucidated. In this study, we exploit the biophysical properties of Shaker-IR mutants T449A/V474C and T449A/V476C to evaluate the status of the activation and inactivation gates during steady-state inactivation and upon locking the channel open with intracellular Cd(2+). We conclude that at negative membrane potentials, the gating scheme of Shaker channels can be refined in two aspects. First, the most likely pathway for the development of steady-state inactivation is C→O→OI [Formula: see text] CI. Second, the OI→CI transition is a prerequisite for recovery from inactivation. These findings are in accordance with the widely accepted view that tight coupling is present between the activation and C-type inactivation gates in Shaker and underscore the role of steady-state inactivation and recovery from inactivation as determinants of excitability. Rockefeller University Press 2020-05-22 /pmc/articles/PMC7398138/ /pubmed/32442242 http://dx.doi.org/10.1085/jgp.202012591 Text en © 2020 Szanto et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/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 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Szanto, Tibor G.
Zakany, Florina
Papp, Ferenc
Varga, Zoltan
Deutsch, Carol J.
Panyi, Gyorgy
The activation gate controls steady-state inactivation and recovery from inactivation in Shaker
title The activation gate controls steady-state inactivation and recovery from inactivation in Shaker
title_full The activation gate controls steady-state inactivation and recovery from inactivation in Shaker
title_fullStr The activation gate controls steady-state inactivation and recovery from inactivation in Shaker
title_full_unstemmed The activation gate controls steady-state inactivation and recovery from inactivation in Shaker
title_short The activation gate controls steady-state inactivation and recovery from inactivation in Shaker
title_sort activation gate controls steady-state inactivation and recovery from inactivation in shaker
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7398138/
https://www.ncbi.nlm.nih.gov/pubmed/32442242
http://dx.doi.org/10.1085/jgp.202012591
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