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Allosteric interactions among voltage-sensor modules of sodium channels probed by scorpion toxin modifiers
Gating of voltage-dependent sodium channels involves coordinated movements of the voltage sensors in the voltage-sensing modules (VSMs) of the four domains (DI-DIV) in response to membrane depolarization. Zhu et al. have recently examined the effects of charge reversal substitutions at the VSM of do...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10081521/ https://www.ncbi.nlm.nih.gov/pubmed/37034138 http://dx.doi.org/10.46439/neurobiology.4.021 |
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author | Gurevitz, Michael Zhorov, Boris S. Dong, Ke |
author_facet | Gurevitz, Michael Zhorov, Boris S. Dong, Ke |
author_sort | Gurevitz, Michael |
collection | PubMed |
description | Gating of voltage-dependent sodium channels involves coordinated movements of the voltage sensors in the voltage-sensing modules (VSMs) of the four domains (DI-DIV) in response to membrane depolarization. Zhu et al. have recently examined the effects of charge reversal substitutions at the VSM of domain III on the action of scorpion alpha- and beta-toxins that intercept the voltage sensors in domains IV and II, respectively. The increased activity of both toxin types on the mutant channels has suggested that the VSM module at domain III interacts allosterically with the VSM modules in domains IV and II during channel gating thus affecting indirectly the action of both scorpion toxin classes. |
format | Online Article Text |
id | pubmed-10081521 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
record_format | MEDLINE/PubMed |
spelling | pubmed-100815212023-04-07 Allosteric interactions among voltage-sensor modules of sodium channels probed by scorpion toxin modifiers Gurevitz, Michael Zhorov, Boris S. Dong, Ke J Neurobiol Physiol Article Gating of voltage-dependent sodium channels involves coordinated movements of the voltage sensors in the voltage-sensing modules (VSMs) of the four domains (DI-DIV) in response to membrane depolarization. Zhu et al. have recently examined the effects of charge reversal substitutions at the VSM of domain III on the action of scorpion alpha- and beta-toxins that intercept the voltage sensors in domains IV and II, respectively. The increased activity of both toxin types on the mutant channels has suggested that the VSM module at domain III interacts allosterically with the VSM modules in domains IV and II during channel gating thus affecting indirectly the action of both scorpion toxin classes. 2022 /pmc/articles/PMC10081521/ /pubmed/37034138 http://dx.doi.org/10.46439/neurobiology.4.021 Text en https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Article Gurevitz, Michael Zhorov, Boris S. Dong, Ke Allosteric interactions among voltage-sensor modules of sodium channels probed by scorpion toxin modifiers |
title | Allosteric interactions among voltage-sensor modules of sodium
channels probed by scorpion toxin modifiers |
title_full | Allosteric interactions among voltage-sensor modules of sodium
channels probed by scorpion toxin modifiers |
title_fullStr | Allosteric interactions among voltage-sensor modules of sodium
channels probed by scorpion toxin modifiers |
title_full_unstemmed | Allosteric interactions among voltage-sensor modules of sodium
channels probed by scorpion toxin modifiers |
title_short | Allosteric interactions among voltage-sensor modules of sodium
channels probed by scorpion toxin modifiers |
title_sort | allosteric interactions among voltage-sensor modules of sodium
channels probed by scorpion toxin modifiers |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10081521/ https://www.ncbi.nlm.nih.gov/pubmed/37034138 http://dx.doi.org/10.46439/neurobiology.4.021 |
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