Harrison J K, Lawton R G, Gnegy M E
Department of Pharmacology, University of Michigan, Ann Arbor 48109.
Biochemistry. 1989 Jul 11;28(14):6023-7. doi: 10.1021/bi00440a045.
A novel photoreactive calmodulin (CaM) derivative was developed and used to label the purified CaM-sensitive adenylate cyclase from bovine cortex. 125I-CaM was conjugated with the heterobifunctional cross-linking agent p-nitrophenyl 3-diazopyruvate (DAPpNP). Spectral data indicated that diazopyruvoyl (DAP) groups were incorporated into the CaM molecule. Iodo-CaM-DAPs behaved like native CaM with respect to (1) Ca2+-dependent enhanced mobility on sodium dodecyl sulfate-polyacrylamide gels and (2) Ca2+-dependent stimulation of adenylate cyclase activity. 125I-CaM-DAP photochemically cross-linked to CaM-binding proteins in a manner that was both Ca2+ dependent and CaM specific. Photolysis of forskolin-agarose-purified adenylate cyclase from bovine cortex with 125I-CaM-DAP produced a single cross-linked product which migrates on sodium dodecyl sulfate-polyacrylamide gels with an apparent molecular weight of approximately 140,000.
一种新型的光反应性钙调蛋白(CaM)衍生物被研发出来,并用于标记从牛大脑皮层纯化得到的对CaM敏感的腺苷酸环化酶。125I-CaM与异双功能交联剂对硝基苯基3-重氮丙酮酸(DAPpNP)偶联。光谱数据表明重氮丙酮酸基(DAP)已掺入CaM分子中。碘代-CaM-DAP在以下方面表现得与天然CaM相似:(1)在十二烷基硫酸钠-聚丙烯酰胺凝胶上,其迁移率依赖于Ca2+增强;(2)对腺苷酸环化酶活性的刺激依赖于Ca2+。125I-CaM-DAP以一种既依赖Ca2+又具有CaM特异性的方式与CaM结合蛋白进行光化学交联。用125I-CaM-DAP对从牛大脑皮层中经福司可林-琼脂糖纯化得到的腺苷酸环化酶进行光解,产生了一种单一的交联产物,该产物在十二烷基硫酸钠-聚丙烯酰胺凝胶上迁移,其表观分子量约为140,000。