Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhou, Changping, Tajima, Nami
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2023
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
_version_ 1785123217055154176
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