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Characterization of the omega-conotoxin-binding molecule in rat brain synaptosomes and cultured neurons.

作者信息

Marqueze B, Martin-Moutot N, Levêque C, Couraud F

机构信息

Laboratoire de Biochimie, CNRS UA 1179, Faculté de Médecine Nord, Marseille, France.

出版信息

Mol Pharmacol. 1988 Aug;34(2):87-90.

PMID:2457794
Abstract

omega-Conotoxin GVIA is a peptide purified from the venom of the marine snail, Conus geographus, that specifically blocks voltage-sensitive calcium channels in neurons. A mono-[125I]iodo-omega-conotoxin was prepared and specific binding to both rat brain synaptosomal membranes and cultured neurons was detected. The interaction was irreversible and the association kinetic constant k was measured at 5-7 X 10(6) M-1 s-1 in synaptosomes and at 2-4 X 10(6) M-1 s-1 on intact neurons. The binding site capacities were 650 and 60 fmol/mg of protein, respectively. No competition was detected with other calcium channel blockers or with toxins acting on Na+ or K+ channels but the binding was lowered by the divalent cations Co2+ and Ca2+. Photoaffinity experiments specifically labeled a single component with an apparent Mr of 222,000 +/- 7,000 in brain synaptosomes and 245,000-300,000 in cultured embryonic neurons.

摘要

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