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Upward movement of IS4 and IIIS4 is a rate-limiting stage in Ca(v)1.2 activation

In order to specify the role of individual S4 segments in Ca(V)1.2 gating, charged residues of segments IS4-IVS4 were replaced by glutamine and the corresponding effects on activation/deactivation of calcium channel currents were analysed. Almost all replacements of charges in IS4 and IIIS4 decrease...

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Autores principales: Beyl, Stanislav, Hohaus, Annette, Andranovits, Stanislav, Timin, Eugen, Hering, Steffen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5138263/
https://www.ncbi.nlm.nih.gov/pubmed/27796578
http://dx.doi.org/10.1007/s00424-016-1895-5
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author Beyl, Stanislav
Hohaus, Annette
Andranovits, Stanislav
Timin, Eugen
Hering, Steffen
author_facet Beyl, Stanislav
Hohaus, Annette
Andranovits, Stanislav
Timin, Eugen
Hering, Steffen
author_sort Beyl, Stanislav
collection PubMed
description In order to specify the role of individual S4 segments in Ca(V)1.2 gating, charged residues of segments IS4-IVS4 were replaced by glutamine and the corresponding effects on activation/deactivation of calcium channel currents were analysed. Almost all replacements of charges in IS4 and IIIS4 decreased the slope of the Boltzmann curve of channel activation (activation curve) while charge neutralisations in IIS4 and IVS4 did not significantly affect the slope. S4 mutations caused either left or rightward shifts of the activation curve, and in wild-type channels, these S4 mutations hardly affected current kinetics. In slowly gating pore (S6) mutants (G432W, A780T, G1193T or A1503G), neutralisations in S4 segments significantly accelerated current kinetics. Likewise in wild type, charge replacements in IS4 and IIIS4 of pore mutants reduced the slope of the activation curves while substitutions of charges in IIS4 and IVS4 had less or no impact. We propose a gating model where the structurally different S4 segments leave their resting positions not simultaneously. Upward movement of segments IS4 and (to a lesser extend) IIIS4 appear to be a rate-limiting stage for releasing the pore gates. These segments carry most of the effective charge for channel activation. Our study suggests that S4 segments of Ca(V)1.2 control the closed state in domain specific manner while stabilizing the open state in a non-specific manner. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00424-016-1895-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-51382632016-12-21 Upward movement of IS4 and IIIS4 is a rate-limiting stage in Ca(v)1.2 activation Beyl, Stanislav Hohaus, Annette Andranovits, Stanislav Timin, Eugen Hering, Steffen Pflugers Arch Ion Channels, Receptors and Transporters In order to specify the role of individual S4 segments in Ca(V)1.2 gating, charged residues of segments IS4-IVS4 were replaced by glutamine and the corresponding effects on activation/deactivation of calcium channel currents were analysed. Almost all replacements of charges in IS4 and IIIS4 decreased the slope of the Boltzmann curve of channel activation (activation curve) while charge neutralisations in IIS4 and IVS4 did not significantly affect the slope. S4 mutations caused either left or rightward shifts of the activation curve, and in wild-type channels, these S4 mutations hardly affected current kinetics. In slowly gating pore (S6) mutants (G432W, A780T, G1193T or A1503G), neutralisations in S4 segments significantly accelerated current kinetics. Likewise in wild type, charge replacements in IS4 and IIIS4 of pore mutants reduced the slope of the activation curves while substitutions of charges in IIS4 and IVS4 had less or no impact. We propose a gating model where the structurally different S4 segments leave their resting positions not simultaneously. Upward movement of segments IS4 and (to a lesser extend) IIIS4 appear to be a rate-limiting stage for releasing the pore gates. These segments carry most of the effective charge for channel activation. Our study suggests that S4 segments of Ca(V)1.2 control the closed state in domain specific manner while stabilizing the open state in a non-specific manner. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00424-016-1895-5) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2016-10-29 2016 /pmc/articles/PMC5138263/ /pubmed/27796578 http://dx.doi.org/10.1007/s00424-016-1895-5 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Ion Channels, Receptors and Transporters
Beyl, Stanislav
Hohaus, Annette
Andranovits, Stanislav
Timin, Eugen
Hering, Steffen
Upward movement of IS4 and IIIS4 is a rate-limiting stage in Ca(v)1.2 activation
title Upward movement of IS4 and IIIS4 is a rate-limiting stage in Ca(v)1.2 activation
title_full Upward movement of IS4 and IIIS4 is a rate-limiting stage in Ca(v)1.2 activation
title_fullStr Upward movement of IS4 and IIIS4 is a rate-limiting stage in Ca(v)1.2 activation
title_full_unstemmed Upward movement of IS4 and IIIS4 is a rate-limiting stage in Ca(v)1.2 activation
title_short Upward movement of IS4 and IIIS4 is a rate-limiting stage in Ca(v)1.2 activation
title_sort upward movement of is4 and iiis4 is a rate-limiting stage in ca(v)1.2 activation
topic Ion Channels, Receptors and Transporters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5138263/
https://www.ncbi.nlm.nih.gov/pubmed/27796578
http://dx.doi.org/10.1007/s00424-016-1895-5
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