Helmeste D M, Hammonds R G, Li C H
Proc Natl Acad Sci U S A. 1986 Jul;83(13):4622-5. doi: 10.1073/pnas.83.13.4622.
A radioligand suitable for crosslinking studies to opioid receptors has been obtained by radioiodination and purification of the monoiodotyrosine-27 derivative of the synthetic human beta-endorphin (beta h-endorphin) analogue [5-leucine]beta h-endorphin. The derivative, [27-[125I]monoiodotyrosine,5-leucine]beta h-endorphin, was crosslinked to human striatal (caudate and putamen) and NG108-15 neuroblastoma-glioma cell membranes by using disuccinimidyl suberate. Sodium dodecyl sulfate/polyacrylamide gel electrophoresis under reducing conditions revealed four specifically labeled bands at 68, 40, 30, and 25 kDa for both human caudate and putamen, whereas NG108-15 cell membranes gave specifically labeled bands at 92, 56, 38, and 23 kDa.
通过对合成的人β-内啡肽(βh-内啡肽)类似物[5-亮氨酸]βh-内啡肽的单碘酪氨酸-27衍生物进行放射性碘化和纯化,获得了一种适用于与阿片受体进行交联研究的放射性配体。该衍生物[27-[¹²⁵I]单碘酪氨酸,5-亮氨酸]βh-内啡肽,通过使用辛二酸二琥珀酰亚胺酯与人纹状体(尾状核和壳核)以及NG108-15神经母细胞瘤-胶质瘤细胞膜进行交联。在还原条件下进行的十二烷基硫酸钠/聚丙烯酰胺凝胶电泳显示,人尾状核和壳核均有四条特异性标记条带,分别位于68、40、30和25 kDa处,而NG108-15细胞膜的特异性标记条带位于92、56、38和23 kDa处。