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蝎毒素阻断对树突毒素敏感的电压激活钾通道。

Charybdotoxin blocks dendrotoxin-sensitive voltage-activated K+ channels.

作者信息

Schweitz H, Stansfeld C E, Bidard J N, Fagni L, Maes P, Lazdunski M

机构信息

Centre de Biochimie du Centre National de la Recherche Scientifique, Nice, France.

出版信息

FEBS Lett. 1989 Jul 3;250(2):519-22. doi: 10.1016/0014-5793(89)80788-4.

Abstract

Charybdotoxin, a short scorpion venom neurotoxin, which was thought to be specific for the blockade of Ca2+-activated K+ channels also blocks a class of voltage-sensitive K+ channels that are known to be the target of other peptide neurotoxins from snake and bee venoms such as dendrotoxin and MCD peptide. Charybdotoxin also inhibits 125I-dendrotoxin and 125I-MCD peptide binding to their receptors. All these effects are observed with an IC50 of about 30 nM.

摘要

卡律蝎毒素是一种短链蝎毒神经毒素,曾被认为对阻断钙激活钾通道具有特异性,它也能阻断一类电压敏感性钾通道,这类通道是蛇毒和蜂毒中其他肽类神经毒素(如树突毒素和MCD肽)的作用靶点。卡律蝎毒素还能抑制125I-树突毒素和125I-MCD肽与其受体的结合。所有这些效应在约30 nM的半数抑制浓度(IC50)下即可观察到。

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