Literature DB >> 17419047

Structural aspects of AMPA receptor activation, desensitization and deactivation.

Kasper B Hansen1, Hongjie Yuan, Stephen F Traynelis.   

Abstract

Glutamate mediates most of the excitatory neurotransmission in the mammalian central nervous system by activating ionotropic glutamate receptors. Structural and functional studies of ionotropic glutamate receptors have offered detailed insight into the mechanism by which these integral membrane proteins function. In particular, advances in our understanding of the atomic structure of the agonist-binding domain have provided new opportunities to consider the conformational changes that take place in a functioning ligand-gated ion channel. Several recent studies have turned up important new ideas about the structural determinants of channel activation, deactivation and desensitization of AMPA receptors. Working hypotheses derived from this structural insight offer a rare opportunity to enrich and guide functional studies.

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Year:  2007        PMID: 17419047     DOI: 10.1016/j.conb.2007.03.014

Source DB:  PubMed          Journal:  Curr Opin Neurobiol        ISSN: 0959-4388            Impact factor:   6.627


  28 in total

Review 1.  Synaptic neurotransmitter-gated receptors.

Authors:  Trevor G Smart; Pierre Paoletti
Journal:  Cold Spring Harb Perspect Biol       Date:  2012-03-01       Impact factor: 10.005

Review 2.  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

3.  TARP subtypes differentially and dose-dependently control synaptic AMPA receptor gating.

Authors:  Aaron D Milstein; Wei Zhou; Siavash Karimzadegan; David S Bredt; Roger A Nicoll
Journal:  Neuron       Date:  2007-09-20       Impact factor: 17.173

4.  A mutation in the Proteosomal Regulatory Particle AAA-ATPase-3 in Arabidopsis impairs the light-specific hypocotyl elongation response elicited by a glutamate receptor agonist, BMAA.

Authors:  Eric D Brenner; Philip Feinberg; Suzan Runko; Gloria M Coruzzi
Journal:  Plant Mol Biol       Date:  2009-05-02       Impact factor: 4.076

5.  Stability of ligand-binding domain dimer assembly controls kainate receptor desensitization.

Authors:  Charu Chaudhry; Matthew C Weston; Peter Schuck; Christian Rosenmund; Mark L Mayer
Journal:  EMBO J       Date:  2009-04-02       Impact factor: 11.598

6.  Asynchronous movements prior to pore opening in NMDA receptors.

Authors:  Rashek Kazi; Quan Gan; Iehab Talukder; Michael Markowitz; Catherine L Salussolia; Lonnie P Wollmuth
Journal:  J Neurosci       Date:  2013-07-17       Impact factor: 6.167

7.  Activation and desensitization induce distinct conformational changes at the extracellular-transmembrane domain interface of the glycine receptor.

Authors:  Qian Wang; Joseph W Lynch
Journal:  J Biol Chem       Date:  2011-09-14       Impact factor: 5.157

8.  Modulation of the dimer interface at ionotropic glutamate-like receptor delta2 by D-serine and extracellular calcium.

Authors:  Kasper B Hansen; Peter Naur; Natalie L Kurtkaya; Anders S Kristensen; Michael Gajhede; Jette S Kastrup; Stephen F Traynelis
Journal:  J Neurosci       Date:  2009-01-28       Impact factor: 6.167

9.  Full domain closure of the ligand-binding core of the ionotropic glutamate receptor iGluR5 induced by the high affinity agonist dysiherbaine and the functional antagonist 8,9-dideoxyneodysiherbaine.

Authors:  Karla Frydenvang; L Leanne Lash; Peter Naur; Pekka A Postila; Darryl S Pickering; Caleb M Smith; Michael Gajhede; Makoto Sasaki; Ryuichi Sakai; Olli T Pentikaïnen; Geoffrey T Swanson; Jette S Kastrup
Journal:  J Biol Chem       Date:  2009-03-18       Impact factor: 5.157

10.  AMPA receptor ligand binding domain mobility revealed by functional cross linking.

Authors:  Andrew J R Plested; Mark L Mayer
Journal:  J Neurosci       Date:  2009-09-23       Impact factor: 6.167

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