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Structure, function, and allosteric modulation of NMDA receptors.

Authors :
Hansen, Kasper B.
Feng Yi
Perszyk, Riley E.
Furukawa, Hiro
Wollmuth, Lonnie P.
Gibb, Alasdair J.
Traynelis, Stephen F.
Source :
Journal of General Physiology. Aug2018, Vol. 150 Issue 8, p1081-1105. 25p.
Publication Year :
2018

Abstract

NMDA-type glutamate receptors are ligand-gated ion channels that mediate a Ca2+-permeable component of excitatory neurotransmission in the central nervous system (CNS). They are expressed throughout the CNS and play key physiological roles in synaptic function, such as synaptic plasticity, learning, and memory. NMDA receptors are also implicated in the pathophysiology of several CNS disorders and more recently have been identified as a locus for disease-associated genomic variation. NMDA receptors exist as a diverse array of subtypes formed by variation in assembly of seven subunits (GluN1, GluN2A-D, and GluN3A-B) into tetrameric receptor complexes. These NMDA receptor subtypes show unique structural features that account for their distinct functional and pharmacological properties allowing precise tuning of their physiological roles. Here, we review the relationship between NMDA receptor structure and function with an emphasis on emerging atomic resolution structures, which begin to explain unique features of this receptor. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00221295
Volume :
150
Issue :
8
Database :
Academic Search Index
Journal :
Journal of General Physiology
Publication Type :
Academic Journal
Accession number :
131267457
Full Text :
https://doi.org/10.1085/jgp.201812032