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Definition of two agonist types at the mammalian cold-activated channel TRPM8
Various TRP channels act as polymodal sensors of thermal and chemical stimuli, but the mechanisms whereby chemical ligands impact on TRP channel gating are poorly understood. Here we show that AITC (allyl isothiocyanate; mustard oil) and menthol represent two distinct types of ligands at the mammali...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4985286/ https://www.ncbi.nlm.nih.gov/pubmed/27449282 http://dx.doi.org/10.7554/eLife.17240 |
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author | Janssens, Annelies Gees, Maarten Toth, Balazs Istvan Ghosh, Debapriya Mulier, Marie Vennekens, Rudi Vriens, Joris Talavera, Karel Voets, Thomas |
author_facet | Janssens, Annelies Gees, Maarten Toth, Balazs Istvan Ghosh, Debapriya Mulier, Marie Vennekens, Rudi Vriens, Joris Talavera, Karel Voets, Thomas |
author_sort | Janssens, Annelies |
collection | PubMed |
description | Various TRP channels act as polymodal sensors of thermal and chemical stimuli, but the mechanisms whereby chemical ligands impact on TRP channel gating are poorly understood. Here we show that AITC (allyl isothiocyanate; mustard oil) and menthol represent two distinct types of ligands at the mammalian cold sensor TRPM8. Kinetic analysis of channel gating revealed that AITC acts by destabilizing the closed channel, whereas menthol stabilizes the open channel, relative to the transition state. Based on these differences, we classify agonists as either type I (menthol-like) or type II (AITC-like), and provide a kinetic model that faithfully reproduces their differential effects. We further demonstrate that type I and type II agonists have a distinct impact on TRPM8 currents and TRPM8-mediated calcium signals in excitable cells. These findings provide a theoretical framework for understanding the differential actions of TRP channel ligands, with important ramifications for TRP channel structure-function analysis and pharmacology. DOI: http://dx.doi.org/10.7554/eLife.17240.001 |
format | Online Article Text |
id | pubmed-4985286 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-49852862016-08-23 Definition of two agonist types at the mammalian cold-activated channel TRPM8 Janssens, Annelies Gees, Maarten Toth, Balazs Istvan Ghosh, Debapriya Mulier, Marie Vennekens, Rudi Vriens, Joris Talavera, Karel Voets, Thomas eLife Biophysics and Structural Biology Various TRP channels act as polymodal sensors of thermal and chemical stimuli, but the mechanisms whereby chemical ligands impact on TRP channel gating are poorly understood. Here we show that AITC (allyl isothiocyanate; mustard oil) and menthol represent two distinct types of ligands at the mammalian cold sensor TRPM8. Kinetic analysis of channel gating revealed that AITC acts by destabilizing the closed channel, whereas menthol stabilizes the open channel, relative to the transition state. Based on these differences, we classify agonists as either type I (menthol-like) or type II (AITC-like), and provide a kinetic model that faithfully reproduces their differential effects. We further demonstrate that type I and type II agonists have a distinct impact on TRPM8 currents and TRPM8-mediated calcium signals in excitable cells. These findings provide a theoretical framework for understanding the differential actions of TRP channel ligands, with important ramifications for TRP channel structure-function analysis and pharmacology. DOI: http://dx.doi.org/10.7554/eLife.17240.001 eLife Sciences Publications, Ltd 2016-07-23 /pmc/articles/PMC4985286/ /pubmed/27449282 http://dx.doi.org/10.7554/eLife.17240 Text en © 2016, Janssens et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biophysics and Structural Biology Janssens, Annelies Gees, Maarten Toth, Balazs Istvan Ghosh, Debapriya Mulier, Marie Vennekens, Rudi Vriens, Joris Talavera, Karel Voets, Thomas Definition of two agonist types at the mammalian cold-activated channel TRPM8 |
title | Definition of two agonist types at the mammalian cold-activated channel TRPM8 |
title_full | Definition of two agonist types at the mammalian cold-activated channel TRPM8 |
title_fullStr | Definition of two agonist types at the mammalian cold-activated channel TRPM8 |
title_full_unstemmed | Definition of two agonist types at the mammalian cold-activated channel TRPM8 |
title_short | Definition of two agonist types at the mammalian cold-activated channel TRPM8 |
title_sort | definition of two agonist types at the mammalian cold-activated channel trpm8 |
topic | Biophysics and Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4985286/ https://www.ncbi.nlm.nih.gov/pubmed/27449282 http://dx.doi.org/10.7554/eLife.17240 |
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