Literature DB >> 15823042

Kinetic mechanism of channel opening of the GluRDflip AMPA receptor.

Gang Li1, Zhenyu Sheng, Zhen Huang, Li Niu.   

Abstract

AMPA-type ionotropic glutamate receptors mediate the majority of fast excitatory neurotransmission in the mammalian central nervous system and are essential for brain functions, such as memory and learning. Dysfunction of these receptors has been implicated in a variety of neurological diseases. Using a laser-pulse photolysis technique, we investigated the channel opening mechanism for GluRD(flip) or GluR4(flip) (i.e., the flip isoform of GluRD), an AMPA receptor subunit. The minimal kinetic mechanism for channel opening is consistent with binding of two glutamate molecules per receptor complex. The GluRD(flip) channel opens with a rate constant of (6.83 +/- 0.74) x 10(4) s(-1) and closes with a rate constant of (3.35 +/- 0.17) x 10(3) s(-1). On the basis of these rate constants, the channel opening probability is calculated to be 0.95 +/- 0.12. Furthermore, the shortest rise time (20-80% of the receptor current response to glutamate) is predicted to be 20 micros, which is approximately 8 times shorter than the previous estimate. These findings suggest that the kinetic property of GluRD(flip) is similar to that of GluR2Q(flip), another fast-activating AMPA receptor subunit.

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Year:  2005        PMID: 15823042     DOI: 10.1021/bi047413n

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  9 in total

1.  Channel-opening kinetic mechanism for human wild-type GluK2 and the M867I mutant kainate receptor.

Authors:  Yan Han; Congzhou Wang; Jae Seon Park; Li Niu
Journal:  Biochemistry       Date:  2010-11-02       Impact factor: 3.162

2.  Potent and selective inhibition of a single alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor subunit by an RNA aptamer.

Authors:  Jae-Seon Park; Congzhou Wang; Yan Han; Zhen Huang; Li Niu
Journal:  J Biol Chem       Date:  2011-03-14       Impact factor: 5.157

3.  Channel-opening kinetic mechanism of wild-type GluK1 kainate receptors and a C-terminal mutant.

Authors:  Yan Han; Congzhou Wang; Jae Seon Park; Li Niu
Journal:  Biochemistry       Date:  2012-01-09       Impact factor: 3.162

4.  Mechanism and site of inhibition of AMPA receptors: pairing a thiadiazole with a 2,3-benzodiazepine scaffold.

Authors:  Congzhou Wang; Yan Han; Andrew Wu; Sándor Sólyom; Li Niu
Journal:  ACS Chem Neurosci       Date:  2013-12-17       Impact factor: 4.418

5.  Energetics of the cleft closing transition and the role of electrostatic interactions in conformational rearrangements of the glutamate receptor ligand binding domain.

Authors:  Tatyana Mamonova; Michael J Yonkunas; Maria G Kurnikova
Journal:  Biochemistry       Date:  2008-09-30       Impact factor: 3.162

6.  Mechanism of inhibition of the GluA2 AMPA receptor channel opening by talampanel and its enantiomer: the stereochemistry of the 4-methyl group on the diazepine ring of 2,3-benzodiazepine derivatives.

Authors:  Congzhou Wang; Li Niu
Journal:  ACS Chem Neurosci       Date:  2013-02-12       Impact factor: 4.418

7.  Hydrophobic Gating of Ion Permeation in Magnesium Channel CorA.

Authors:  Chris Neale; Nilmadhab Chakrabarti; Pawel Pomorski; Emil F Pai; Régis Pomès
Journal:  PLoS Comput Biol       Date:  2015-07-16       Impact factor: 4.475

8.  Stargazin and γ4 slow the channel opening and closing rates of GluA4 AMPA receptors.

Authors:  Vincen D Pierce; Li Niu
Journal:  Sci Rep       Date:  2019-07-02       Impact factor: 4.379

9.  Mechanism of inhibition of the GluA1 AMPA receptor channel opening by the 2,3-benzodiazepine compound GYKI 52466 and a N-methyl-carbamoyl derivative.

Authors:  Andrew Wu; Congzhou Wang; Li Niu
Journal:  Biochemistry       Date:  2014-05-01       Impact factor: 3.162

  9 in total

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