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Rapid constriction of the selectivity filter underlies C-type inactivation in the KcsA potassium channel

C-type inactivation is a time-dependent process observed in many K(+) channels whereby prolonged activation by an external stimulus leads to a reduction in ionic conduction. While C-type inactivation is thought to be a result of a constriction of the selectivity filter, the local dynamics of the pro...

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Autores principales: Li, Jing, Ostmeyer, Jared, Cuello, Luis G., Perozo, Eduardo, Roux, Benoît
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6168234/
https://www.ncbi.nlm.nih.gov/pubmed/30072373
http://dx.doi.org/10.1085/jgp.201812082
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author Li, Jing
Ostmeyer, Jared
Cuello, Luis G.
Perozo, Eduardo
Roux, Benoît
author_facet Li, Jing
Ostmeyer, Jared
Cuello, Luis G.
Perozo, Eduardo
Roux, Benoît
author_sort Li, Jing
collection PubMed
description C-type inactivation is a time-dependent process observed in many K(+) channels whereby prolonged activation by an external stimulus leads to a reduction in ionic conduction. While C-type inactivation is thought to be a result of a constriction of the selectivity filter, the local dynamics of the process remain elusive. Here, we use molecular dynamics (MD) simulations of the KcsA channel to elucidate the nature of kinetically delayed activation/inactivation gating coupling. Microsecond-scale MD simulations based on the truncated form of the KcsA channel (C-terminal domain deleted) provide a first glimpse of the onset of C-type inactivation. We observe over multiple trajectories that the selectivity filter consistently undergoes a spontaneous and rapid (within 1–2 µs) transition to a constricted conformation when the intracellular activation gate is fully open, but remains in the conductive conformation when the activation gate is closed or partially open. Multidimensional umbrella sampling potential of mean force calculations and nonequilibrium voltage-driven simulations further confirm these observations. Electrophysiological measurements show that the truncated form of the KcsA channel inactivates faster and greater than full-length KcsA, which is consistent with truncated KcsA opening to a greater degree because of the absence of the C-terminal domain restraint. Together, these results imply that the observed kinetics underlying activation/inactivation gating reflect a rapid conductive-to-constricted transition of the selectivity filter that is allosterically controlled by the slow opening of the intracellular gate.
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spelling pubmed-61682342019-04-01 Rapid constriction of the selectivity filter underlies C-type inactivation in the KcsA potassium channel Li, Jing Ostmeyer, Jared Cuello, Luis G. Perozo, Eduardo Roux, Benoît J Gen Physiol Research Articles C-type inactivation is a time-dependent process observed in many K(+) channels whereby prolonged activation by an external stimulus leads to a reduction in ionic conduction. While C-type inactivation is thought to be a result of a constriction of the selectivity filter, the local dynamics of the process remain elusive. Here, we use molecular dynamics (MD) simulations of the KcsA channel to elucidate the nature of kinetically delayed activation/inactivation gating coupling. Microsecond-scale MD simulations based on the truncated form of the KcsA channel (C-terminal domain deleted) provide a first glimpse of the onset of C-type inactivation. We observe over multiple trajectories that the selectivity filter consistently undergoes a spontaneous and rapid (within 1–2 µs) transition to a constricted conformation when the intracellular activation gate is fully open, but remains in the conductive conformation when the activation gate is closed or partially open. Multidimensional umbrella sampling potential of mean force calculations and nonequilibrium voltage-driven simulations further confirm these observations. Electrophysiological measurements show that the truncated form of the KcsA channel inactivates faster and greater than full-length KcsA, which is consistent with truncated KcsA opening to a greater degree because of the absence of the C-terminal domain restraint. Together, these results imply that the observed kinetics underlying activation/inactivation gating reflect a rapid conductive-to-constricted transition of the selectivity filter that is allosterically controlled by the slow opening of the intracellular gate. Rockefeller University Press 2018-10-01 /pmc/articles/PMC6168234/ /pubmed/30072373 http://dx.doi.org/10.1085/jgp.201812082 Text en © 2018 Li et al. http://www.rupress.org/termshttps://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 (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 Research Articles
Li, Jing
Ostmeyer, Jared
Cuello, Luis G.
Perozo, Eduardo
Roux, Benoît
Rapid constriction of the selectivity filter underlies C-type inactivation in the KcsA potassium channel
title Rapid constriction of the selectivity filter underlies C-type inactivation in the KcsA potassium channel
title_full Rapid constriction of the selectivity filter underlies C-type inactivation in the KcsA potassium channel
title_fullStr Rapid constriction of the selectivity filter underlies C-type inactivation in the KcsA potassium channel
title_full_unstemmed Rapid constriction of the selectivity filter underlies C-type inactivation in the KcsA potassium channel
title_short Rapid constriction of the selectivity filter underlies C-type inactivation in the KcsA potassium channel
title_sort rapid constriction of the selectivity filter underlies c-type inactivation in the kcsa potassium channel
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6168234/
https://www.ncbi.nlm.nih.gov/pubmed/30072373
http://dx.doi.org/10.1085/jgp.201812082
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