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Structural insights into NMDA receptor pharmacology
N-methyl-d-aspartate receptors (NMDARs) comprise a subfamily of ionotropic glutamate receptors that form heterotetrameric ligand-gated ion channels and play fundamental roles in neuronal processes such as synaptic signaling and plasticity. Given their critical roles in brain function and their thera...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10586783/ https://www.ncbi.nlm.nih.gov/pubmed/37431773 http://dx.doi.org/10.1042/BST20230122 |
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author | Zhou, Changping Tajima, Nami |
author_facet | Zhou, Changping Tajima, Nami |
author_sort | Zhou, Changping |
collection | PubMed |
description | N-methyl-d-aspartate receptors (NMDARs) comprise a subfamily of ionotropic glutamate receptors that form heterotetrameric ligand-gated ion channels and play fundamental roles in neuronal processes such as synaptic signaling and plasticity. Given their critical roles in brain function and their therapeutic importance, enormous research efforts have been devoted to elucidating the structure and function of these receptors and developing novel therapeutics. Recent studies have resolved the structures of NMDARs in multiple functional states, and have revealed the detailed gating mechanism, which was found to be distinct from that of other ionotropic glutamate receptors. This review provides a brief overview of the recent progress in understanding the structures of NMDARs and the mechanisms underlying their function, focusing on subtype-specific, ligand-induced conformational dynamics. |
format | Online Article Text |
id | pubmed-10586783 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-105867832023-10-20 Structural insights into NMDA receptor pharmacology Zhou, Changping Tajima, Nami Biochem Soc Trans Review Articles N-methyl-d-aspartate receptors (NMDARs) comprise a subfamily of ionotropic glutamate receptors that form heterotetrameric ligand-gated ion channels and play fundamental roles in neuronal processes such as synaptic signaling and plasticity. Given their critical roles in brain function and their therapeutic importance, enormous research efforts have been devoted to elucidating the structure and function of these receptors and developing novel therapeutics. Recent studies have resolved the structures of NMDARs in multiple functional states, and have revealed the detailed gating mechanism, which was found to be distinct from that of other ionotropic glutamate receptors. This review provides a brief overview of the recent progress in understanding the structures of NMDARs and the mechanisms underlying their function, focusing on subtype-specific, ligand-induced conformational dynamics. Portland Press Ltd. 2023-08-31 2023-07-11 /pmc/articles/PMC10586783/ /pubmed/37431773 http://dx.doi.org/10.1042/BST20230122 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Articles Zhou, Changping Tajima, Nami Structural insights into NMDA receptor pharmacology |
title | Structural insights into NMDA receptor pharmacology |
title_full | Structural insights into NMDA receptor pharmacology |
title_fullStr | Structural insights into NMDA receptor pharmacology |
title_full_unstemmed | Structural insights into NMDA receptor pharmacology |
title_short | Structural insights into NMDA receptor pharmacology |
title_sort | structural insights into nmda receptor pharmacology |
topic | Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10586783/ https://www.ncbi.nlm.nih.gov/pubmed/37431773 http://dx.doi.org/10.1042/BST20230122 |
work_keys_str_mv | AT zhouchangping structuralinsightsintonmdareceptorpharmacology AT tajimanami structuralinsightsintonmdareceptorpharmacology |