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来自绿曼巴蛇(Dendroaspis angusticeps)的抗毒蕈碱毒素

Anti-muscarinic toxins from Dendroaspis angusticeps.

作者信息

Liang J S, Carsi-Gabrenas J, Krajewski J L, McCafferty J M, Purkerson S L, Santiago M P, Strauss W L, Valentine H H, Potter L T

机构信息

Department of Molecular and Cellular Pharmacology, University of Miami School of Medicine, FL 33101, USA.

出版信息

Toxicon. 1996 Nov-Dec;34(11-12):1257-67. doi: 10.1016/s0041-0101(96)00109-2.

Abstract

Toxins from the venom of the African green mamba, Dendroaspis angusticeps, fulfill a major need for selective ligands for some of the five genetically defined subtypes of muscarinic acetylcholine receptors (m1-m5). Two toxins have been found that are highly selective antagonists for m1 and m4 receptors (m1-toxin and m4-toxin, respectively). Two other toxins (MT1 and MT2) bind with high affinity to both m1 and m4 receptors, and are agonists. Components of the venom also modify the binding of radiolabeled antagonists to m2 receptors, but an m2-selective toxin has not yet been isolated, m1-Toxin can bind to m1 receptors at the same time as typical competitive antagonists, suggesting that this toxin binds to the N-terminal and outer loops of m1 receptor molecules, rather than within the receptor pocket where typical agonists and antagonists bind. The binding of toxins to the outer parts of receptor molecules probably accounts for their much higher specificity for individual receptor subtypes than is seen with smaller ligands. Toxins are useful for identifying, counting, localizing, activating and blocking m1 and m4 receptors with high specificity.

摘要

非洲绿曼巴蛇(Dendroaspis angusticeps)毒液中的毒素,满足了对毒蕈碱型乙酰胆碱受体(m1 - m5)五个基因定义亚型中的某些亚型的选择性配体的主要需求。已发现两种毒素分别是m1和m4受体的高选择性拮抗剂(分别为m1毒素和m4毒素)。另外两种毒素(MT1和MT2)与m1和m4受体都具有高亲和力,且为激动剂。毒液成分也会改变放射性标记拮抗剂与m2受体的结合,但尚未分离出m2选择性毒素。m1毒素可与典型竞争性拮抗剂同时结合m1受体,这表明该毒素结合于m1受体分子的N端和外环,而非典型激动剂和拮抗剂结合的受体口袋内。毒素与受体分子外部的结合,可能解释了它们对单个受体亚型的特异性远高于较小配体的原因。毒素可用于高特异性地识别、计数、定位、激活和阻断m1和m4受体。

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