Hammonds R G, Westphal M, Li C H
Biochem Biophys Res Commun. 1985 May 16;128(3):1310-4. doi: 10.1016/0006-291x(85)91083-6.
A photoaffinity reagent 2-nitro-4-azidophenylsulfenyl chloride (2,4-NAPS-Cl) and synthetic analogs of human beta-endorphin (beta h-EP) were employed to demonstrate the presence of receptor sites specific for beta h-EP but of non-opioid character in a human neuroblastoma cell line (IMR-32). The radioactive photoaffinity probe was carried out using [125I-Tyr1,2,4-NAPS-Trp27]-beta h-EP and IMR-32 cell membranes. After solubilization with sodium dodecyl sulfate (SDS) and SDS polyacrylamide gel electrophoresis, a single labelled protein band was identified with a molecular weight of 72,000. Labelling was blocked by beta h-EP or beta h-EP-(6-31) but remained in the presence of beta h-EP-(1-27). The specificity of this band is thus identical to that of the non-opioid site previously characterized. Various nonionic or zwitterionic detergents did not extract the labelled non-opioid site.
使用光亲和试剂2-硝基-4-叠氮基苯基硫代氯(2,4-NAPS-Cl)和人β-内啡肽(βh-EP)的合成类似物,来证明在人神经母细胞瘤细胞系(IMR-32)中存在对βh-EP具有特异性但具有非阿片样物质特性的受体位点。使用[125I-Tyr1,2,4-NAPS-Trp27]-βh-EP和IMR-32细胞膜进行放射性光亲和探针实验。用十二烷基硫酸钠(SDS)溶解并经SDS聚丙烯酰胺凝胶电泳后,鉴定出一条分子量为72,000的单一标记蛋白带。标记被βh-EP或βh-EP-(6-31)阻断,但在βh-EP-(1-27)存在时仍保留。因此,这条带的特异性与先前表征的非阿片样物质位点相同。各种非离子或两性离子去污剂均未提取出标记的非阿片样物质位点。