Literature DB >> 9655513

The location of the gate in the acetylcholine receptor channel.

G G Wilson1, A Karlin.   

Abstract

The cation-conducting channel of the nicotinic acetylcholine (ACh) receptor is lined by the first (M1) and second (M2) membrane-spanning segments of each of its five subunits. Six consecutive residues, alphaS239 to alphaT244, in the alpha subunit M1-M2 loop and at the intracellular end of M2 were mutated to cysteine. The accessibility of the substituted cysteines were probed with small, cationic, sulfhydryl-specific reagents added extracellularly and intracellularly. In the closed state of the channel, there is a barrier to these reagents added from either side between alphaG240 and alphaT244. ACh induces the removal of this barrier, which acts as an activation gate. The residues alphaG240, alphaE241, alphaK242, and alphaT244 line a narrow part of the channel, in which this gate is located.

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Year:  1998        PMID: 9655513     DOI: 10.1016/s0896-6273(00)80506-1

Source DB:  PubMed          Journal:  Neuron        ISSN: 0896-6273            Impact factor:   17.173


  67 in total

Review 1.  Inherited and experimentally induced changes in gating kinetics of muscle nicotinic acetylcholine receptor.

Authors:  C Bouzat; F J Barrantes
Journal:  J Mol Neurosci       Date:  1999 Aug-Oct       Impact factor: 3.444

2.  M2 pore mutations convert the glycine receptor channel from being anion- to cation-selective.

Authors:  A Keramidas; A J Moorhouse; C R French; P R Schofield; P H Barry
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3.  A molecular link between inward rectification and calcium permeability of neuronal nicotinic acetylcholine alpha3beta4 and alpha4beta2 receptors.

Authors:  A P Haghighi; E Cooper
Journal:  J Neurosci       Date:  2000-01-15       Impact factor: 6.167

4.  Allosteric activation mechanism of the alpha 1 beta 2 gamma 2 gamma-aminobutyric acid type A receptor revealed by mutation of the conserved M2 leucine.

Authors:  Y Chang; D S Weiss
Journal:  Biophys J       Date:  1999-11       Impact factor: 4.033

5.  Location of a constriction in the lumen of a transmembrane pore by targeted covalent attachment of polymer molecules.

Authors:  L Movileanu; S Cheley; S Howorka; O Braha; H Bayley
Journal:  J Gen Physiol       Date:  2001-03       Impact factor: 4.086

6.  Single channel analysis of conductance and rectification in cation-selective, mutant glycine receptor channels.

Authors:  Andrew J Moorhouse; Angelo Keramidas; Andrey Zaykin; Peter R Schofield; Peter H Barry
Journal:  J Gen Physiol       Date:  2002-05       Impact factor: 4.086

7.  Cation-selective mutations in the M2 domain of the inhibitory glycine receptor channel reveal determinants of ion-charge selectivity.

Authors:  Angelo Keramidas; Andrew J Moorhouse; Kerrie D Pierce; Peter R Schofield; Peter H Barry
Journal:  J Gen Physiol       Date:  2002-05       Impact factor: 4.086

8.  Microscopic kinetics and energetics distinguish GABA(A) receptor agonists from antagonists.

Authors:  M V Jones; P Jonas; Y Sahara; G L Westbrook
Journal:  Biophys J       Date:  2001-11       Impact factor: 4.033

9.  Structural determinants of fast desensitization and desensitization-deactivation coupling in GABAa receptors.

Authors:  M T Bianchi; K F Haas; R L Macdonald
Journal:  J Neurosci       Date:  2001-02-15       Impact factor: 6.167

10.  Structural effects of quinacrine binding in the open channel of the acetylcholine receptor.

Authors:  Yong Yu; Lei Shi; Arthur Karlin
Journal:  Proc Natl Acad Sci U S A       Date:  2003-03-18       Impact factor: 11.205

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