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K(+) channel gating: C-type inactivation is enhanced by calcium or lanthanum outside

Many voltage-gated K(+) channels exhibit C-type inactivation. This typically slow process has been hypothesized to result from dilation of the outer-most ring of the carbonyls in the selectivity filter, destroying this ring’s ability to bind K(+) with high affinity. We report here strong enhancement...

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Autores principales: Armstrong, Clay M., Hoshi, Toshinori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4144669/
https://www.ncbi.nlm.nih.gov/pubmed/25156116
http://dx.doi.org/10.1085/jgp.201411223
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author Armstrong, Clay M.
Hoshi, Toshinori
author_facet Armstrong, Clay M.
Hoshi, Toshinori
author_sort Armstrong, Clay M.
collection PubMed
description Many voltage-gated K(+) channels exhibit C-type inactivation. This typically slow process has been hypothesized to result from dilation of the outer-most ring of the carbonyls in the selectivity filter, destroying this ring’s ability to bind K(+) with high affinity. We report here strong enhancement of C-type inactivation upon extracellular addition of 10–40 mM Ca(2+) or 5–50 µM La(3+). These multivalent cations mildly increase the rate of C-type inactivation during depolarization and markedly promote inactivation and/or suppress recovery when membrane voltage (V(m)) is at resting levels (−80 to −100 mV). At −80 mV with 40 mM Ca(2+) and 0 mM K(+) externally, ShBΔN channels with the mutation T449A inactivate almost completely within 2 min or less with no pulsing. This behavior is observed only in those mutants that show C-type inactivation on depolarization and is distinct from the effects of Ca(2+) and La(3+) on activation (opening and closing of the V(m)-controlled gate), i.e., slower activation of K(+) channels and a positive shift of the mid-voltage of activation. The Ca(2+)/La(3+) effects on C-type inactivation are antagonized by extracellular K(+) in the low millimolar range. This, together with the known ability of Ca(2+) and La(3+) to block inward current through K(+) channels at negative voltage, strongly suggests that Ca(2+)/La(3+) acts at the outer mouth of the selectivity filter. We propose that at −80 mV, Ca(2+) or La(3+) ions compete effectively with K(+) at the channel’s outer mouth and prevent K(+) from stabilizing the filter’s outer carbonyl ring.
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spelling pubmed-41446692015-03-01 K(+) channel gating: C-type inactivation is enhanced by calcium or lanthanum outside Armstrong, Clay M. Hoshi, Toshinori J Gen Physiol Research Articles Many voltage-gated K(+) channels exhibit C-type inactivation. This typically slow process has been hypothesized to result from dilation of the outer-most ring of the carbonyls in the selectivity filter, destroying this ring’s ability to bind K(+) with high affinity. We report here strong enhancement of C-type inactivation upon extracellular addition of 10–40 mM Ca(2+) or 5–50 µM La(3+). These multivalent cations mildly increase the rate of C-type inactivation during depolarization and markedly promote inactivation and/or suppress recovery when membrane voltage (V(m)) is at resting levels (−80 to −100 mV). At −80 mV with 40 mM Ca(2+) and 0 mM K(+) externally, ShBΔN channels with the mutation T449A inactivate almost completely within 2 min or less with no pulsing. This behavior is observed only in those mutants that show C-type inactivation on depolarization and is distinct from the effects of Ca(2+) and La(3+) on activation (opening and closing of the V(m)-controlled gate), i.e., slower activation of K(+) channels and a positive shift of the mid-voltage of activation. The Ca(2+)/La(3+) effects on C-type inactivation are antagonized by extracellular K(+) in the low millimolar range. This, together with the known ability of Ca(2+) and La(3+) to block inward current through K(+) channels at negative voltage, strongly suggests that Ca(2+)/La(3+) acts at the outer mouth of the selectivity filter. We propose that at −80 mV, Ca(2+) or La(3+) ions compete effectively with K(+) at the channel’s outer mouth and prevent K(+) from stabilizing the filter’s outer carbonyl ring. The Rockefeller University Press 2014-09 /pmc/articles/PMC4144669/ /pubmed/25156116 http://dx.doi.org/10.1085/jgp.201411223 Text en © 2014 Armstrong and Hoshi 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 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Research Articles
Armstrong, Clay M.
Hoshi, Toshinori
K(+) channel gating: C-type inactivation is enhanced by calcium or lanthanum outside
title K(+) channel gating: C-type inactivation is enhanced by calcium or lanthanum outside
title_full K(+) channel gating: C-type inactivation is enhanced by calcium or lanthanum outside
title_fullStr K(+) channel gating: C-type inactivation is enhanced by calcium or lanthanum outside
title_full_unstemmed K(+) channel gating: C-type inactivation is enhanced by calcium or lanthanum outside
title_short K(+) channel gating: C-type inactivation is enhanced by calcium or lanthanum outside
title_sort k(+) channel gating: c-type inactivation is enhanced by calcium or lanthanum outside
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4144669/
https://www.ncbi.nlm.nih.gov/pubmed/25156116
http://dx.doi.org/10.1085/jgp.201411223
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