Shimazaki K, Hirata Y, Nakajima T, Kawai N
Department of Neurobiology, Tokyo Metropolitan Institute for Neurosciences, Japan.
Neurosci Lett. 1990 Jun 22;114(1):1-4. doi: 10.1016/0304-3940(90)90418-9.
Joro spider toxin (JSTX), a specific blocker of glutamate receptors, was conjugated with biotin. Using the avidin-biotin complex method, specific binding sites of biotinylated JSTX were demonstrated in the cerebellum and hippocampus of the rat. In the cerebellum, strong binding of biotinyl JSTX was observed on perikarya and dendrites of the Purkinje cells with much less binding in the granular cell layer. In the hippocampus, a dense staining was observed in the pyramidal cell layer, with more heavy binding in CA3 than in other sectors of Ammon's horn. The area of distribution of biotinyl JSTX binding sites corresponded well with that of receptors preferentially activated by quisqualate.
乔罗蜘蛛毒素(JSTX)是一种谷氨酸受体的特异性阻滞剂,它与生物素结合。利用抗生物素蛋白-生物素复合物方法,在大鼠的小脑和海马体中证实了生物素化JSTX的特异性结合位点。在小脑中,观察到生物素化JSTX在浦肯野细胞的胞体和树突上有强烈结合,而在颗粒细胞层中的结合较少。在海马体中,锥体细胞层观察到密集染色,在海马角的CA3区比其他区域的结合更重。生物素化JSTX结合位点的分布区域与优先被喹啉酸盐激活的受体的分布区域非常吻合。