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标记的毒蕈碱毒素125I-MT1与大鼠脑毒蕈碱M1受体的结合。

Binding of the labelled muscarinic toxin 125I-MT1 to rat brain muscarinic M1 receptors.

作者信息

Waelbroeck M, De Neef P, Domenach V, Vandermeers-Piret M C, Vandermeers A

机构信息

Department of Biochemistry and Nutrition, School of Medicine, Université Libre de Bruxelles, Belgium.

出版信息

Eur J Pharmacol. 1996 Jun 3;305(1-3):187-92. doi: 10.1016/0014-2999(96)00136-7.

Abstract

The green mamba (Dendroaspis angusticeps) "muscarinic toxin', MT1, was radioiodinated by the chloramine T method. 125I-MT1 labelled the muscarinic M1 receptor subtype with a very good selectivity in rat brain. It had no preference for the receptor states with high or low affinity for agonists, and was not affected by Gpp(NH)p addition to the incubation medium. The 125I-MT1 binding was reversible, with a half life of 45 min at 25 degrees C. The effect of competitive and allosteric muscarinic antagonists on 125I-MT1 binding and dissociation can be rationalized by assuming that the radioiodinated toxin is able to label the muscarinic (acetylcholine) binding site.

摘要

绿曼巴蛇(黑曼巴蛇)“毒蕈碱毒素”MT1通过氯胺T法进行放射性碘化。125I-MT1在大鼠脑中以非常好的选择性标记毒蕈碱M1受体亚型。它对激动剂具有高亲和力或低亲和力的受体状态没有偏好,并且不受向孵育培养基中添加Gpp(NH)p的影响。125I-MT1的结合是可逆的,在25℃下半衰期为45分钟。通过假设放射性碘化毒素能够标记毒蕈碱(乙酰胆碱)结合位点,可以合理解释竞争性和变构毒蕈碱拮抗剂对125I-MT1结合和解离的影响。

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