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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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Formato: | Texto |
Lenguaje: | English |
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Molecular Diversity Preservation International
2010
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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. |
format | Text |
id | pubmed-2866490 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Molecular Diversity Preservation International |
record_format | MEDLINE/PubMed |
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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