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The coupling of the M2 muscarinic receptor to its G protein is voltage dependent

G protein coupled receptors (GPCRs) participate in the majority of signal transduction processes in the body. Specifically, the binding of an external agonist promotes coupling of the GPCR to its G protein and this, in turn, induces downstream signaling. Recently, it was shown that agonist binding t...

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Autores principales: Ben-Chaim, Yair, Broide, Chava, Parnas, Hanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6822938/
https://www.ncbi.nlm.nih.gov/pubmed/31671117
http://dx.doi.org/10.1371/journal.pone.0224367
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author Ben-Chaim, Yair
Broide, Chava
Parnas, Hanna
author_facet Ben-Chaim, Yair
Broide, Chava
Parnas, Hanna
author_sort Ben-Chaim, Yair
collection PubMed
description G protein coupled receptors (GPCRs) participate in the majority of signal transduction processes in the body. Specifically, the binding of an external agonist promotes coupling of the GPCR to its G protein and this, in turn, induces downstream signaling. Recently, it was shown that agonist binding to the M2 muscarinic receptor (M2R) and to other GPCRs is voltage dependent. Here we examine, whether the coupling of the M2R to its G protein is also voltage-dependent. We first show, in Xenopus oocytes, that the activity of the M2R in the absence of agonist (constitutive activity) can be used to report the coupling. We then show that the coupling is, by itself, voltage dependent. This novel finding is of physiological importance, as it shows that the actual signal transduction, whose first step is the coupling of the GPCR to its cognate G protein, is voltage dependent.
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spelling pubmed-68229382019-11-12 The coupling of the M2 muscarinic receptor to its G protein is voltage dependent Ben-Chaim, Yair Broide, Chava Parnas, Hanna PLoS One Research Article G protein coupled receptors (GPCRs) participate in the majority of signal transduction processes in the body. Specifically, the binding of an external agonist promotes coupling of the GPCR to its G protein and this, in turn, induces downstream signaling. Recently, it was shown that agonist binding to the M2 muscarinic receptor (M2R) and to other GPCRs is voltage dependent. Here we examine, whether the coupling of the M2R to its G protein is also voltage-dependent. We first show, in Xenopus oocytes, that the activity of the M2R in the absence of agonist (constitutive activity) can be used to report the coupling. We then show that the coupling is, by itself, voltage dependent. This novel finding is of physiological importance, as it shows that the actual signal transduction, whose first step is the coupling of the GPCR to its cognate G protein, is voltage dependent. Public Library of Science 2019-10-31 /pmc/articles/PMC6822938/ /pubmed/31671117 http://dx.doi.org/10.1371/journal.pone.0224367 Text en © 2019 Ben-Chaim et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Ben-Chaim, Yair
Broide, Chava
Parnas, Hanna
The coupling of the M2 muscarinic receptor to its G protein is voltage dependent
title The coupling of the M2 muscarinic receptor to its G protein is voltage dependent
title_full The coupling of the M2 muscarinic receptor to its G protein is voltage dependent
title_fullStr The coupling of the M2 muscarinic receptor to its G protein is voltage dependent
title_full_unstemmed The coupling of the M2 muscarinic receptor to its G protein is voltage dependent
title_short The coupling of the M2 muscarinic receptor to its G protein is voltage dependent
title_sort coupling of the m2 muscarinic receptor to its g protein is voltage dependent
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6822938/
https://www.ncbi.nlm.nih.gov/pubmed/31671117
http://dx.doi.org/10.1371/journal.pone.0224367
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