Schaap D, Parker P J
Ludwig Institute for Cancer Research, London, Great Britain.
J Biol Chem. 1990 May 5;265(13):7301-7.
Of the recently described members of the protein kinase C (PKC) family (-delta, -epsilon, -zeta), no detailed properties of the purified enzymes have been presented. Here we describe the expression of PKC-epsilon in insect cells using a baculovirus vector. The recombinant enzyme has been purified to homogeneity by sequential chromatography on DEAE-cellulose, serine-Sepharose, Mono Q, and Superose 12; the protein shows a molecular mass of 90 kDa on sodium dodecyl sulfate-polyacrylamide gel electrophoresis. PKC-epsilon is dependent upon phospholipid and diacylglycerol (or phorbol esters) for activity and displays a pattern of specificity for these effectors similar to other PKC isotypes. Similarly, inhibition of PKC-epsilon by staurosporine and H-7 parallels inhibition of other PKC isotypes. However, unlike PKC-alpha, -beta, and -gamma, PKC-epsilon shows no dependence upon Ca2+. Furthermore, the substrate specificity of PKC-epsilon is quite different from other characterized PKCs. The importance of functional diversity within the PKC family is discussed.
在最近描述的蛋白激酶C(PKC)家族成员(-δ、-ε、-ζ)中,尚未有关于纯化酶详细特性的报道。在此,我们描述了利用杆状病毒载体在昆虫细胞中表达PKC-ε的情况。通过在DEAE-纤维素、丝氨酸-琼脂糖、Mono Q和Superose 12上依次进行层析,已将重组酶纯化至同质;该蛋白在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳上显示分子量为90 kDa。PKC-ε的活性依赖于磷脂和二酰基甘油(或佛波酯),并且对这些效应物表现出与其他PKC亚型相似的特异性模式。同样,星形孢菌素和H-7对PKC-ε的抑制作用与对其他PKC亚型的抑制作用相似。然而,与PKC-α、-β和-γ不同,PKC-ε不依赖于Ca2+。此外,PKC-ε的底物特异性与其他已表征的PKC有很大不同。文中讨论了PKC家族内功能多样性的重要性。