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Muscarinic receptor oligomerization

G protein-coupled receptors (GPCRs) have been classically described as monomeric entities that function by binding in a 1:1 stoichiometric ratio to both ligand and downstream signalling proteins. However, in recent years, a growing number of studies has supported the hypothesis that these receptors...

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Detalles Bibliográficos
Autores principales: Marsango, Sara, Ward, Richard J., Alvarez-Curto, Elisa, Milligan, Graeme
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pergamon Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6078712/
https://www.ncbi.nlm.nih.gov/pubmed/29146505
http://dx.doi.org/10.1016/j.neuropharm.2017.11.023
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author Marsango, Sara
Ward, Richard J.
Alvarez-Curto, Elisa
Milligan, Graeme
author_facet Marsango, Sara
Ward, Richard J.
Alvarez-Curto, Elisa
Milligan, Graeme
author_sort Marsango, Sara
collection PubMed
description G protein-coupled receptors (GPCRs) have been classically described as monomeric entities that function by binding in a 1:1 stoichiometric ratio to both ligand and downstream signalling proteins. However, in recent years, a growing number of studies has supported the hypothesis that these receptors can interact to form dimers and higher order oligomers although the molecular basis for these interactions, the overall quaternary arrangements and the functional importance of GPCR oligomerization remain topics of intense speculation. Muscarinic acetylcholine receptors belong to class A of the GPCR family. Each muscarinic receptor subtype has its own particular distribution throughout the central and peripheral nervous systems. In the central nervous system, muscarinic receptors regulate several sensory, cognitive, and motor functions while, in the peripheral nervous system, they are involved in the regulation of heart rate, stimulation of glandular secretion and smooth muscle contraction. Muscarinic acetylcholine receptors have long been used as a model for the study of GPCR structure and function and to address aspects of GPCR dimerization using a broad range of approaches. In this review, the prevailing knowledge regarding the quaternary arrangement for the various muscarinic acetylcholine receptors has been summarized by discussing work ranging from initial results obtained using more traditional biochemical approaches to those generated with more modern biophysical techniques. This article is part of the Special Issue entitled ‘Neuropharmacology on Muscarinic Receptors’.
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spelling pubmed-60787122018-08-10 Muscarinic receptor oligomerization Marsango, Sara Ward, Richard J. Alvarez-Curto, Elisa Milligan, Graeme Neuropharmacology Article G protein-coupled receptors (GPCRs) have been classically described as monomeric entities that function by binding in a 1:1 stoichiometric ratio to both ligand and downstream signalling proteins. However, in recent years, a growing number of studies has supported the hypothesis that these receptors can interact to form dimers and higher order oligomers although the molecular basis for these interactions, the overall quaternary arrangements and the functional importance of GPCR oligomerization remain topics of intense speculation. Muscarinic acetylcholine receptors belong to class A of the GPCR family. Each muscarinic receptor subtype has its own particular distribution throughout the central and peripheral nervous systems. In the central nervous system, muscarinic receptors regulate several sensory, cognitive, and motor functions while, in the peripheral nervous system, they are involved in the regulation of heart rate, stimulation of glandular secretion and smooth muscle contraction. Muscarinic acetylcholine receptors have long been used as a model for the study of GPCR structure and function and to address aspects of GPCR dimerization using a broad range of approaches. In this review, the prevailing knowledge regarding the quaternary arrangement for the various muscarinic acetylcholine receptors has been summarized by discussing work ranging from initial results obtained using more traditional biochemical approaches to those generated with more modern biophysical techniques. This article is part of the Special Issue entitled ‘Neuropharmacology on Muscarinic Receptors’. Pergamon Press 2018-07-01 /pmc/articles/PMC6078712/ /pubmed/29146505 http://dx.doi.org/10.1016/j.neuropharm.2017.11.023 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Marsango, Sara
Ward, Richard J.
Alvarez-Curto, Elisa
Milligan, Graeme
Muscarinic receptor oligomerization
title Muscarinic receptor oligomerization
title_full Muscarinic receptor oligomerization
title_fullStr Muscarinic receptor oligomerization
title_full_unstemmed Muscarinic receptor oligomerization
title_short Muscarinic receptor oligomerization
title_sort muscarinic receptor oligomerization
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6078712/
https://www.ncbi.nlm.nih.gov/pubmed/29146505
http://dx.doi.org/10.1016/j.neuropharm.2017.11.023
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