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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
16
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pubmed:dateCreated |
2001-4-17
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pubmed:abstractText |
We investigated the mechanism of interaction of individual L-type channel amino acid residues with dihydropyridines within a dihydropyridine-sensitive alpha1A subunit (alpha1A(DHP)). Mutation of individual residues in repeat III and expression in Xenopus oocytes revealed that Thr(1393) is not required for dihydropyridine interaction but that bulky side chains (tyrosine, phenylalanine) in this position sterically inhibit dihydropyridine coordination. In position 1397 a side chain carbonyl group was required for high antagonist sensitivity. Agonist function required the complete amide group of a glutamine residue. Val(1516) and Met(1512) side chains were required for agonist (Val(1516)) and antagonist (Val(1516), Met(1512)) sensitivity. Replacement of Ile(1504) and Ile(1507) by alpha1A phenylalanines was tolerated. Substitution of Thr(1393) by phenylalanine or Val(1516) by alanine introduced voltage dependence of antagonist action into alpha1A(DHP), suggesting that these residues form part of a mechanism mediating voltage dependence of dihydropyridine sensitivity. Our data provide important insight into dihydropyridine binding to alpha1A(DHP) which could facilitate the development of alpha1A-selective modulators. By modulating P/Q-type Ca(2+) channels such drugs could serve as new anti-migraine therapeutics.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/1,4-dihydropyridine,
http://linkedlifedata.com/resource/pubmed/chemical/Alanine,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium Channel Blockers,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium Channels, L-Type,
http://linkedlifedata.com/resource/pubmed/chemical/Dihydropyridines,
http://linkedlifedata.com/resource/pubmed/chemical/Isoleucine,
http://linkedlifedata.com/resource/pubmed/chemical/Isradipine,
http://linkedlifedata.com/resource/pubmed/chemical/Methionine,
http://linkedlifedata.com/resource/pubmed/chemical/Phenylalanine,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Subunits,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Valine
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0021-9258
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
20
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pubmed:volume |
276
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
12730-5
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11278630-Alanine,
pubmed-meshheading:11278630-Amino Acid Sequence,
pubmed-meshheading:11278630-Amino Acid Substitution,
pubmed-meshheading:11278630-Animals,
pubmed-meshheading:11278630-Binding Sites,
pubmed-meshheading:11278630-Calcium Channel Blockers,
pubmed-meshheading:11278630-Calcium Channels, L-Type,
pubmed-meshheading:11278630-Dihydropyridines,
pubmed-meshheading:11278630-Female,
pubmed-meshheading:11278630-Isoleucine,
pubmed-meshheading:11278630-Isradipine,
pubmed-meshheading:11278630-Kinetics,
pubmed-meshheading:11278630-Methionine,
pubmed-meshheading:11278630-Models, Molecular,
pubmed-meshheading:11278630-Molecular Sequence Data,
pubmed-meshheading:11278630-Mutagenesis, Site-Directed,
pubmed-meshheading:11278630-Oocytes,
pubmed-meshheading:11278630-Phenylalanine,
pubmed-meshheading:11278630-Protein Structure, Secondary,
pubmed-meshheading:11278630-Protein Subunits,
pubmed-meshheading:11278630-Recombinant Proteins,
pubmed-meshheading:11278630-Valine,
pubmed-meshheading:11278630-Xenopus laevis
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pubmed:year |
2001
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pubmed:articleTitle |
Mechanism of dihydropyridine interaction with critical binding residues of L-type Ca2+ channel alpha 1 subunits.
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pubmed:affiliation |
Institut für Biochemische Pharmakologie, Peter-Maystrasse 1, A-6020 Innsbruck, Austria.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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