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Nat Chem Biol. 2017 Dec;13(12):1232-1238. doi: 10.1038/nchembio.2487. Epub 2017 Oct 9.

The structure-energy landscape of NMDA receptor gating.

Author information

1
Center for Membrane Biology, Department of Biochemistry and Molecular Biology, University of Texas Health Science Center at Houston, Houston, Texas, USA.
2
Biochemistry and Molecular Biology Graduate Program, Graduate School of Biomedical Sciences, University of Texas Health Science Center at Houston, Houston, Texas, USA.
3
Department of Chemistry, Rice University, Houston, Texas, USA.
4
Department of Electrical and Computer Engineering, Rice University, Houston, Texas, USA.

Abstract

N-Methyl-D-aspartate (NMDA) receptors are the main calcium-permeable excitatory receptors in the mammalian central nervous system. The NMDA receptor gating is complex, exhibiting multiple closed, open, and desensitized states; however, central questions regarding the conformations and energetics of the transmembrane domains as they relate to the gating states are still unanswered. Here, using single-molecule Förster resonance energy transfer (smFRET), we map the energy landscape of the first transmembrane segment of the Rattus norvegicus NMDA receptor under resting and various liganded conditions. These results show kinetically and structurally distinct changes associated with apo, agonist-bound, and inhibited receptors linked by a linear mechanism of gating at this site. Furthermore, the smFRET data suggest that allosteric inhibition by zinc occurs by an uncoupling of the agonist-induced changes at the extracellular domains from the gating motions leading to an apo-like state, while dizocilpine, a pore blocker, stabilizes multiple closely packed transmembrane states.

PMID:
28991238
PMCID:
PMC5698143
DOI:
10.1038/nchembio.2487
[Indexed for MEDLINE]
Free PMC Article

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