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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2020
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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. |
format | Online Article Text |
id | pubmed-7398138 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
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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