Chloride ions stabilize the glutamate-induced active state of the metabotropic glutamate receptor 3.

Amélie S Tora, Xavier Rovira, Anne-Marinette Cao, Alexandre Cabayé, Linnéa Olofsson, Fanny Malhaire, Pauline Scholler, Hayeon Baik, Ann Van Eeckhaut, Ilse Smolders, Philippe Rondard, Emmanuel Margeat, Francine Acher, Jean-Philippe Pin, Cyril Goudet

Journal: Neuropharmacology 2019;140():275-286

PMID: 30102917

Abstract

Due to the essential roles of glutamate, detection and response to a large range of extracellular concentrations of this excitatory amino acid are necessary for the fine-tuning of brain functions. Metabotropic glutamate receptors (mGluRs) are implicated in shaping the activity of many synapses in the central nervous system. Among the eight mGluR subtypes, there is increasing interest in studying the mGlu receptor which has recently been linked to various diseases, including psychiatric disorders. This receptor displays striking functional properties, with a high and, often, full basal activity, making its study elusive in heterologous systems. Here, we demonstrate that Cl ions exert strong positive allosteric modulation of glutamate on the mGlu receptor. We have also identified the molecular and structural determinants lying behind this allostery: a unique interactive "chloride-lock" network. Indeed, Cl ions dramatically stabilize the glutamate-induced active state of the extracellular domain of the mGlu receptor. Thus, the mGlu receptors' large basal activity does not correspond to a constitutive activity in absence of agonist. Instead, it results mostly from a Clmediated amplified response to low ambient glutamate concentrations, such as those measured in cell media. This strong interaction between glutamate and Cl ions allows the mGlu receptor to sense and efficiently react to sub-micromolar concentrations of glutamate, making it the most sensitive member of mGluR family.

Copyright © 2018. Published by Elsevier Ltd.

Address: IGF, CNRS, INSERM, Univ. de Montpellier, Montpellier, F-34094, Montpellier, France.; IGF, CNRS, INSERM, Univ. de Montpellier, Montpellier, F-34094, Montpellier, France; Present Address: Molecular Photopharmacology Research Group, The Tissue Repair and Regeneration Laboratory, University of Vic - Central University of Catalonia, C. de La Laura,13, 08500, Vic, Spain.; Centre de Biochimie Structurale (CBS), INSERM, CNRS, Université de Montpellier, F-34094, Montpellier, France.; Laboratoire de Chimie et Biochimie Pharmacologiques et Toxicologiques, CNRS UMR8601, Université Paris Descartes, Sorbonne Paris Cité, F-75270, Paris Cedex 6, France.; Research Group Experimental Pharmacology (EFAR/FASC), Center for Neurosciences (C4N), Vrije Universiteit Brussel (VUB), 1090, Brussel, Belgium.; Laboratoire de Chimie et Biochimie Pharmacologiques et Toxicologiques, CNRS UMR8601, Université Paris Descartes, Sorbonne Paris Cité, F-75270, Paris Cedex 6, France. Electronic address: [email protected].; IGF, CNRS, INSERM, Univ. de Montpellier, Montpellier, F-34094, Montpellier, France. Electronic address: [email protected].; IGF, CNRS, INSERM, Univ. de Montpellier, Montpellier, F-34094, Montpellier, France. Electronic address: [email protected].

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