Literature DB >> 15306812

Reaction mechanism determines NMDA receptor response to repetitive stimulation.

Gabriela Popescu1, Antoine Robert, James R Howe, Anthony Auerbach.   

Abstract

At central excitatory synapses, N-methyl-D-aspartate (NMDA) receptors, which have a high affinity for glutamate, produce a slowly rising synaptic current in response to a single transmitter pulse and an additional current after a second, closely timed stimulus. Here we show, by examining the kinetics of transmitter binding and channel gating in single-channel currents from recombinant NR1/NR2A receptors, that the synaptic response to trains of impulses is determined by the molecular reaction mechanism of the receptor. The rate constants estimated for the activation reaction predict that, after binding neurotransmitter, receptors hesitate for approximately 4 ms in a closed high-affinity conformation before they either proceed towards opening or release neurotransmitter, with about equal probabilities. Because only about half of the initially fully occupied receptors become active, repetitive stimulation elicits currents with distinct waveforms depending on pulse frequency. This high-affinity/low-efficiency activation mechanism might serve as a link between stimulation frequency and the directionality of the ensuing synaptic plasticity.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15306812     DOI: 10.1038/nature02775

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  83 in total

1.  GluN1-specific redox effects on the kinetic mechanism of NMDA receptor activation.

Authors:  Iehab Talukder; Rashek Kazi; Lonnie P Wollmuth
Journal:  Biophys J       Date:  2011-11-15       Impact factor: 4.033

Review 2.  Modes of glutamate receptor gating.

Authors:  Gabriela K Popescu
Journal:  J Physiol       Date:  2011-11-21       Impact factor: 5.182

Review 3.  Glutamate receptor ion channels: structure, regulation, and function.

Authors:  Stephen F Traynelis; Lonnie P Wollmuth; Chris J McBain; Frank S Menniti; Katie M Vance; Kevin K Ogden; Kasper B Hansen; Hongjie Yuan; Scott J Myers; Ray Dingledine
Journal:  Pharmacol Rev       Date:  2010-09       Impact factor: 25.468

4.  Stationary gating of GluN1/GluN2B receptors in intact membrane patches.

Authors:  Stacy A Amico-Ruvio; Gabriela K Popescu
Journal:  Biophys J       Date:  2010-04-07       Impact factor: 4.033

5.  Kinetic contributions to gating by interactions unique to N-methyl-D-aspartate (NMDA) receptors.

Authors:  William F Borschel; Kirstie A Cummings; LeeAnn K Tindell; Gabriela K Popescu
Journal:  J Biol Chem       Date:  2015-09-14       Impact factor: 5.157

6.  Maximum likelihood fitting of single channel NMDA activity with a mechanism composed of independent dimers of subunits.

Authors:  Stephanie Schorge; Sergio Elenes; David Colquhoun
Journal:  J Physiol       Date:  2005-10-13       Impact factor: 5.182

7.  Allosteric interaction between zinc and glutamate binding domains on NR2A causes desensitization of NMDA receptors.

Authors:  Kevin Erreger; Stephen F Traynelis
Journal:  J Physiol       Date:  2005-09-15       Impact factor: 5.182

8.  The relationship between agonist potency and AMPA receptor kinetics.

Authors:  Wei Zhang; Antoine Robert; Stine B Vogensen; James R Howe
Journal:  Biophys J       Date:  2006-05-26       Impact factor: 4.033

9.  Mode switching is the major mechanism of ligand regulation of InsP3 receptor calcium release channels.

Authors:  Lucian Ionescu; Carl White; King-Ho Cheung; Jianwei Shuai; Ian Parker; John E Pearson; J Kevin Foskett; Don-On Daniel Mak
Journal:  J Gen Physiol       Date:  2007-11-12       Impact factor: 4.086

10.  Hodgkin-Huxley-Katz Prize Lecture: Genetic and pharmacological control of glutamate receptor channel through a highly conserved gating motif.

Authors:  Riley E Perszyk; Scott J Myers; Hongjie Yuan; Alasdair J Gibb; Hiro Furukawa; Alexander I Sobolevsky; Stephen F Traynelis
Journal:  J Physiol       Date:  2020-06-15       Impact factor: 5.182

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.