Structural insights into NMDA receptor pharmacology

被引:8
|
作者
Zhou, Changping [1 ]
Tajima, Nami [1 ]
机构
[1] Case Western Reserve Univ, Dept Physiol & Biophys, Cleveland, OH 44106 USA
基金
美国国家卫生研究院;
关键词
D-ASPARTATE RECEPTOR; PROTEIN-KINASE-II; POSITIVE ALLOSTERIC MODULATORS; AMINO-TERMINAL DOMAIN; EXTRACELLULAR VESTIBULE; SUBUNIT ARRANGEMENT; CRYSTAL-STRUCTURE; GATING MECHANISM; ZINC INHIBITION; BINDING DOMAIN;
D O I
10.1042/BST20230122
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:1713 / 1731
页数:19
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