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The Outer Vestibule of the Na(+) Channel–Toxin Receptor and Modulator of Permeation as Well as Gating

The outer vestibule of voltage-gated Na(+) channels is formed by extracellular loops connecting the S5 and S6 segments of all four domains (“P-loops”), which fold back into the membrane. Classically, this structure has been implicated in the control of ion permeation and in toxin blockage. However,...

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Autores principales: Cervenka, René, Zarrabi, Touran, Lukacs, Peter, Todt, Hannes
Formato: Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2866490/
https://www.ncbi.nlm.nih.gov/pubmed/20479982
http://dx.doi.org/10.3390/md8041373
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author Cervenka, René
Zarrabi, Touran
Lukacs, Peter
Todt, Hannes
author_facet Cervenka, René
Zarrabi, Touran
Lukacs, Peter
Todt, Hannes
author_sort Cervenka, René
collection PubMed
description The outer vestibule of voltage-gated Na(+) channels is formed by extracellular loops connecting the S5 and S6 segments of all four domains (“P-loops”), which fold back into the membrane. Classically, this structure has been implicated in the control of ion permeation and in toxin blockage. However, conformational changes of the outer vestibule may also result in alterations in gating, as suggested by several P-loop mutations that gave rise to gating changes. Moreover, partial pore block by mutated toxins may reverse gating changes induced by mutations. Therefore, toxins that bind to the outer vestibule can be used to modulate channel gating.
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spelling pubmed-28664902010-05-17 The Outer Vestibule of the Na(+) Channel–Toxin Receptor and Modulator of Permeation as Well as Gating Cervenka, René Zarrabi, Touran Lukacs, Peter Todt, Hannes Mar Drugs Review The outer vestibule of voltage-gated Na(+) channels is formed by extracellular loops connecting the S5 and S6 segments of all four domains (“P-loops”), which fold back into the membrane. Classically, this structure has been implicated in the control of ion permeation and in toxin blockage. However, conformational changes of the outer vestibule may also result in alterations in gating, as suggested by several P-loop mutations that gave rise to gating changes. Moreover, partial pore block by mutated toxins may reverse gating changes induced by mutations. Therefore, toxins that bind to the outer vestibule can be used to modulate channel gating. Molecular Diversity Preservation International 2010-04-21 /pmc/articles/PMC2866490/ /pubmed/20479982 http://dx.doi.org/10.3390/md8041373 Text en © 2010 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Cervenka, René
Zarrabi, Touran
Lukacs, Peter
Todt, Hannes
The Outer Vestibule of the Na(+) Channel–Toxin Receptor and Modulator of Permeation as Well as Gating
title The Outer Vestibule of the Na(+) Channel–Toxin Receptor and Modulator of Permeation as Well as Gating
title_full The Outer Vestibule of the Na(+) Channel–Toxin Receptor and Modulator of Permeation as Well as Gating
title_fullStr The Outer Vestibule of the Na(+) Channel–Toxin Receptor and Modulator of Permeation as Well as Gating
title_full_unstemmed The Outer Vestibule of the Na(+) Channel–Toxin Receptor and Modulator of Permeation as Well as Gating
title_short The Outer Vestibule of the Na(+) Channel–Toxin Receptor and Modulator of Permeation as Well as Gating
title_sort outer vestibule of the na(+) channel–toxin receptor and modulator of permeation as well as gating
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2866490/
https://www.ncbi.nlm.nih.gov/pubmed/20479982
http://dx.doi.org/10.3390/md8041373
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