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生理温度下不同苯二氮䓬受体的光亲和标记

Photoaffinity labeling of different benzodiazepine receptors at physiological temperature.

作者信息

Eichinger A, Sieghart W

出版信息

J Neurochem. 1984 Dec;43(6):1745-8. doi: 10.1111/j.1471-4159.1984.tb06103.x.

Abstract

Irreversible labeling of benzodiazepine receptors in membranes from cerebellum or hippocampus was compared at 0 degrees C using [3H]flunitrazepam as a photoaffinity ligand. [3H]Flunitrazepam reproducibly and irreversibly labeled mainly one protein (P51) in cerebellum and at least two proteins (P51 and P55) in hippocampus at both temperatures. Differential inhibition at 37 degrees C of irreversible [3H]flunitrazepam binding to the individual proteins by several selective benzodiazepine receptor ligands supports the hypothesis that P51 and P55 are associated with different benzodiazepine receptors.

摘要

使用[3H]氟硝西泮作为光亲和配体,在0摄氏度下比较了小脑或海马膜中苯二氮卓受体的不可逆标记。在这两个温度下,[3H]氟硝西泮可重复且不可逆地标记小脑主要一种蛋白质(P51)和海马至少两种蛋白质(P51和P55)。几种选择性苯二氮卓受体配体在37摄氏度下对不可逆的[3H]氟硝西泮与单个蛋白质结合的差异抑制支持了P51和P55与不同苯二氮卓受体相关的假说。

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