Literature DB >> 8405401

Identification of 1,4-dihydropyridine binding domains within the primary structure of the alpha 1 subunit of the skeletal muscle L-type calcium channel.

H Kalasz1, T Watanabe, H Yabana, K Itagaki, K Naito, H Nakayama, A Schwartz, P L Vaghy.   

Abstract

Calcium channel blockers are drugs that bind to the alpha 1 subunit of L-type calcium channels and selectively inhibit ion movements through these channels. Determination of the mechanism of channel blockade requires localization of drug-binding sites within the primary structure of the receptor. In this study the 1,4-dihydropyridine-binding site of the membrane bound receptor has been identified. The covalently labeled receptor was purified and digested with trypsin. The labeled peptide fragments were immunoprecipitated with sequence-directed antibodies. The data indicate the existence of at least three distinct dihydropyridine-binding domains within the primary structure of the alpha 1 subunit.

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Year:  1993        PMID: 8405401     DOI: 10.1016/0014-5793(93)80321-k

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  8 in total

1.  Binding constants determined from Ca2+ current responses to rapid applications and washouts of nifedipine in frog cardiac myocytes.

Authors:  P F Méry; L Hove-Madsen; J L Mazet; R Hanf; R Fischmeister
Journal:  J Physiol       Date:  1996-07-01       Impact factor: 5.182

2.  Structural model of a synthetic Ca2+ channel with bound Ca2+ ions and dihydropyridine ligand.

Authors:  B S Zhorov; V S Ananthanarayanan
Journal:  Biophys J       Date:  1996-01       Impact factor: 4.033

3.  Malignant-hyperthermia susceptibility is associated with a mutation of the alpha 1-subunit of the human dihydropyridine-sensitive L-type voltage-dependent calcium-channel receptor in skeletal muscle.

Authors:  N Monnier; V Procaccio; P Stieglitz; J Lunardi
Journal:  Am J Hum Genet       Date:  1997-06       Impact factor: 11.025

4.  Two stable cell lines for screening of calcium channel blockers.

Authors:  C Seisenberger; A Welling; A Schuster; F Hofmann
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1995-12       Impact factor: 3.000

Review 5.  Calcium Channel CaVα₁ Splice Isoforms - Tissue Specificity and Drug Action.

Authors:  Diane Lipscombe; Arturo Andrade
Journal:  Curr Mol Pharmacol       Date:  2015       Impact factor: 3.339

6.  Construction of a high-affinity receptor site for dihydropyridine agonists and antagonists by single amino acid substitutions in a non-L-type Ca2+ channel.

Authors:  G H Hockerman; B Z Peterson; E Sharp; T N Tanada; T Scheuer; W A Catterall
Journal:  Proc Natl Acad Sci U S A       Date:  1997-12-23       Impact factor: 11.205

7.  The IVS6 segment of the L-type calcium channel is critical for the action of dihydropyridines and phenylalkylamines.

Authors:  A Schuster; L Lacinová; N Klugbauer; H Ito; L Birnbaumer; F Hofmann
Journal:  EMBO J       Date:  1996-05-15       Impact factor: 11.598

8.  Functional architecture of the inner pore of a voltage-gated Ca2+ channel.

Authors:  Xiao-Guang Zhen; Cheng Xie; Aileen Fitzmaurice; Carl E Schoonover; Eleza T Orenstein; Jian Yang
Journal:  J Gen Physiol       Date:  2005-09       Impact factor: 4.086

  8 in total

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