Literature DB >> 14610080

How fast does the GluR1Qflip channel open?

Gang Li1, Li Niu.   

Abstract

Opening of a ligand-gated ion channel is the step at which the binding of a neurotransmitter is transduced into the electrical signal by allowing ions to flow through the transmembrane channel, thereby altering the postsynaptic membrane potential. We report the kinetics for the opening of the GluR1Qflip channel, an alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor subunit of the ionotropic glutamate receptors. Using a laser-pulse photolysis technique that permits glutamate to be liberated photolytically from gamma-O-(alpha-carboxy-2-nitrobenzyl)glutamate (caged glutamate) with a time constant of approximately 30 micros, we show that, after the binding of glutamate, the channel opened with a rate constant of (2.9 +/- 0.2) x 10(4) s(-1) and closed with a rate constant of (2.1 +/- 0.1) x 10(3) s(-1). The observed shortest rise time (20-80% of the receptor current response), i.e. the fastest time by which the GluR1Qflip channel can open, was predicted to be 35 micros. This value is three times shorter than those previously reported. The minimal kinetic mechanism for channel opening consists of binding of two glutamate molecules, with the channel-opening probability being 0.93 +/- 0.10. These findings identify GluR1Qflip as one of the temporally efficient receptors that transduce the binding of chemical signals (i.e. glutamate) into an electrical impulse.

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Year:  2003        PMID: 14610080     DOI: 10.1074/jbc.M310410200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  18 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.  Mechanism of inhibition of GluA2 AMPA receptor channel opening by 2,3-benzodiazepine derivatives: functional consequences of replacing a 7,8-methylenedioxy with a 7,8-ethylenedioxy moiety.

Authors:  Mohammad S Qneibi; Nicola Micale; Silvana Grasso; Li Niu
Journal:  Biochemistry       Date:  2012-02-13       Impact factor: 3.162

3.  Mechanism of inhibition of the GluA2 AMPA receptor channel opening: consequences of adding an N-3 methylcarbamoyl group to the diazepine ring of 2,3-benzodiazepine derivatives.

Authors:  Congzhou Wang; Zhenyu Sheng; Li Niu
Journal:  Biochemistry       Date:  2011-07-28       Impact factor: 3.162

4.  Long-range coupling in an allosteric receptor revealed by mutant cycle analysis.

Authors:  Kristin R Gleitsman; Jai A P Shanata; Shawnalea J Frazier; Henry A Lester; Dennis A Dougherty
Journal:  Biophys J       Date:  2009-04-22       Impact factor: 4.033

5.  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

6.  Characterizing the energetic states of the GluR2 ligand binding domain core-dimer.

Authors:  Michael Yonkunas; Maria Kurnikova
Journal:  Biophys J       Date:  2011-01-19       Impact factor: 4.033

7.  Mechanism of Inhibition of the GluA2 AMPA Receptor Channel Opening: the Role of 4-Methyl versus 4-Carbonyl Group on the Diazepine Ring of 2,3-Benzodiazepine Derivatives.

Authors:  Mark Ritz; Congzhou Wang; Nicola Micale; Roberta Ettari; Li Niu
Journal:  ACS Chem Neurosci       Date:  2011-05-12       Impact factor: 4.418

8.  A kainate receptor-selective RNA aptamer.

Authors:  William Jaremko; Zhen Huang; Nicholas Karl; Vincen D Pierce; Janet Lynch; Li Niu
Journal:  J Biol Chem       Date:  2020-03-11       Impact factor: 5.157

9.  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

10.  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

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