Literature DB >> 10691288

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

C Bouzat1, F J Barrantes.   

Abstract

Ligand-gated ion channels (LGIC) allow rapid responses in the nervous system. The nicotonic acetylcholine receptor (AChR) has been the model for structure-function relationship studies on this superfamily. The AChR undergoes the following functional events: 1. Binding of the neurotransmitter. 2. Opening of the ion channel. 3. Conduction of ions across the pore. 4. Desensitization. The equilibrium among these processes can be perturbed by alteration in the primary structure of the AChR or by the presence of pharmacological agents. Changes in the primary sequence leading to modifications in gating kinetics may occur in association with physiological or pathological processes. Such changes can also be genetically engineered to gain insights into structure-function relationships.

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Year:  1999        PMID: 10691288     DOI: 10.1385/JMN:13:1-2:1

Source DB:  PubMed          Journal:  J Mol Neurosci        ISSN: 0895-8696            Impact factor:   3.444


  70 in total

1.  Evidence that the M2 membrane-spanning region lines the ion channel pore of the nicotinic receptor.

Authors:  R J Leonard; C G Labarca; P Charnet; N Davidson; H A Lester
Journal:  Science       Date:  1988-12-16       Impact factor: 47.728

2.  Structural basis of the different gating kinetics of fetal and adult acetylcholine receptors.

Authors:  C Bouzat; N Bren; S M Sine
Journal:  Neuron       Date:  1994-12       Impact factor: 17.173

3.  Primary structure of alpha-subunit precursor of Torpedo californica acetylcholine receptor deduced from cDNA sequence.

Authors:  M Noda; H Takahashi; T Tanabe; M Toyosato; Y Furutani; T Hirose; M Asai; S Inayama; T Miyata; S Numa
Journal:  Nature       Date:  1982-10-28       Impact factor: 49.962

4.  Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches.

Authors:  O P Hamill; A Marty; E Neher; B Sakmann; F J Sigworth
Journal:  Pflugers Arch       Date:  1981-08       Impact factor: 3.657

5.  A newly recognized congenital myasthenic syndrome attributed to a prolonged open time of the acetylcholine-induced ion channel.

Authors:  A G Engel; E H Lambert; D M Mulder; C F Torres; K Sahashi; T E Bertorini; J N Whitaker
Journal:  Ann Neurol       Date:  1982-06       Impact factor: 10.422

6.  Amphipathic analysis and possible formation of the ion channel in an acetylcholine receptor.

Authors:  J Finer-Moore; R M Stroud
Journal:  Proc Natl Acad Sci U S A       Date:  1984-01       Impact factor: 11.205

7.  The noncompetitive blocker [(3)H]chlorpromazine labels segment M2 but not segment M1 of the nicotinic acetylcholine receptor alpha-subunit.

Authors:  J Giraudat; J Gali; F Revah; J Changeux; P Haumont; F Lederer
Journal:  FEBS Lett       Date:  1989-08-14       Impact factor: 4.124

8.  Mutations in different functional domains of the human muscle acetylcholine receptor alpha subunit in patients with the slow-channel congenital myasthenic syndrome.

Authors:  R Croxen; C Newland; D Beeson; H Oosterhuis; G Chauplannaz; A Vincent; J Newsom-Davis
Journal:  Hum Mol Genet       Date:  1997-05       Impact factor: 6.150

9.  Mapping the lipid-exposed regions in the Torpedo californica nicotinic acetylcholine receptor.

Authors:  M P Blanton; J B Cohen
Journal:  Biochemistry       Date:  1992-04-21       Impact factor: 3.162

10.  The noncompetitive blocker [3H]chlorpromazine labels three amino acids of the acetylcholine receptor gamma subunit: implications for the alpha-helical organization of regions MII and for the structure of the ion channel.

Authors:  F Revah; J L Galzi; J Giraudat; P Y Haumont; F Lederer; J P Changeux
Journal:  Proc Natl Acad Sci U S A       Date:  1990-06       Impact factor: 11.205

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