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Functional properties and toxin pharmacology of a dorsal root ganglion sodium channel viewed through its voltage sensors
The voltage-activated sodium (Nav) channel Nav1.9 is expressed in dorsal root ganglion (DRG) neurons where it is believed to play an important role in nociception. Progress in revealing the functional properties and pharmacological sensitivities of this non-canonical Nav channel has been slow becaus...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3135324/ https://www.ncbi.nlm.nih.gov/pubmed/21670206 http://dx.doi.org/10.1085/jgp.201110614 |
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author | Bosmans, Frank Puopolo, Michelino Martin-Eauclaire, Marie-France Bean, Bruce P. Swartz, Kenton J. |
author_facet | Bosmans, Frank Puopolo, Michelino Martin-Eauclaire, Marie-France Bean, Bruce P. Swartz, Kenton J. |
author_sort | Bosmans, Frank |
collection | PubMed |
description | The voltage-activated sodium (Nav) channel Nav1.9 is expressed in dorsal root ganglion (DRG) neurons where it is believed to play an important role in nociception. Progress in revealing the functional properties and pharmacological sensitivities of this non-canonical Nav channel has been slow because attempts to express this channel in a heterologous expression system have been unsuccessful. Here, we use a protein engineering approach to dissect the contributions of the four Nav1.9 voltage sensors to channel function and pharmacology. We define individual S3b–S4 paddle motifs within each voltage sensor, and show that they can sense changes in membrane voltage and drive voltage sensor activation when transplanted into voltage-activated potassium channels. We also find that the paddle motifs in Nav1.9 are targeted by animal toxins, and that these toxins alter Nav1.9-mediated currents in DRG neurons. Our results demonstrate that slowly activating and inactivating Nav1.9 channels have functional and pharmacological properties in common with canonical Nav channels, but also show distinctive pharmacological sensitivities that can potentially be exploited for developing novel treatments for pain. |
format | Online Article Text |
id | pubmed-3135324 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-31353242012-01-01 Functional properties and toxin pharmacology of a dorsal root ganglion sodium channel viewed through its voltage sensors Bosmans, Frank Puopolo, Michelino Martin-Eauclaire, Marie-France Bean, Bruce P. Swartz, Kenton J. J Gen Physiol Article The voltage-activated sodium (Nav) channel Nav1.9 is expressed in dorsal root ganglion (DRG) neurons where it is believed to play an important role in nociception. Progress in revealing the functional properties and pharmacological sensitivities of this non-canonical Nav channel has been slow because attempts to express this channel in a heterologous expression system have been unsuccessful. Here, we use a protein engineering approach to dissect the contributions of the four Nav1.9 voltage sensors to channel function and pharmacology. We define individual S3b–S4 paddle motifs within each voltage sensor, and show that they can sense changes in membrane voltage and drive voltage sensor activation when transplanted into voltage-activated potassium channels. We also find that the paddle motifs in Nav1.9 are targeted by animal toxins, and that these toxins alter Nav1.9-mediated currents in DRG neurons. Our results demonstrate that slowly activating and inactivating Nav1.9 channels have functional and pharmacological properties in common with canonical Nav channels, but also show distinctive pharmacological sensitivities that can potentially be exploited for developing novel treatments for pain. The Rockefeller University Press 2011-07 /pmc/articles/PMC3135324/ /pubmed/21670206 http://dx.doi.org/10.1085/jgp.201110614 Text en Copyright © 2011 by the Rockefeller University Press 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 | Article Bosmans, Frank Puopolo, Michelino Martin-Eauclaire, Marie-France Bean, Bruce P. Swartz, Kenton J. Functional properties and toxin pharmacology of a dorsal root ganglion sodium channel viewed through its voltage sensors |
title | Functional properties and toxin pharmacology of a dorsal root ganglion sodium channel viewed through its voltage sensors |
title_full | Functional properties and toxin pharmacology of a dorsal root ganglion sodium channel viewed through its voltage sensors |
title_fullStr | Functional properties and toxin pharmacology of a dorsal root ganglion sodium channel viewed through its voltage sensors |
title_full_unstemmed | Functional properties and toxin pharmacology of a dorsal root ganglion sodium channel viewed through its voltage sensors |
title_short | Functional properties and toxin pharmacology of a dorsal root ganglion sodium channel viewed through its voltage sensors |
title_sort | functional properties and toxin pharmacology of a dorsal root ganglion sodium channel viewed through its voltage sensors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3135324/ https://www.ncbi.nlm.nih.gov/pubmed/21670206 http://dx.doi.org/10.1085/jgp.201110614 |
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