Friedrich T D, Ingram V M
Massachusetts Institute of Technology, Department of Biology, Cambridge.
Biochim Biophys Acta. 1989 Jul 21;992(1):41-8. doi: 10.1016/0304-4165(89)90048-2.
Three casein kinase activities have been resolved by column chromatography of HeLa cell nuclear extracts. In addition to casein kinases NI and NII, which have been described in other cell types, HeLa nuclei contain a third casein kinase activity which we have named NIII. NIII is a cyclic nucleotide-independent casein kinase which uses either Mg2+ or Mn2+ as a divalent cation, but is inhibited by increasing NaCl concentrations in the presence of Mg2+ and has optimal activity at 50 mM NaCl in the presence of Mn2+. In Mg2+, NIII uses only ATP as a phosphate donor, but in Mn2+ NIII transfers phosphate from either ATP or GTP. NIII phosphorylates the serine and threonine residues of casein, but does not phosphorylate phosvitin or calf thymus histones.
通过对HeLa细胞核提取物进行柱层析,已分离出三种酪蛋白激酶活性。除了在其他细胞类型中已描述的酪蛋白激酶NI和NII外,HeLa细胞核还含有第三种酪蛋白激酶活性,我们将其命名为NIII。NIII是一种不依赖环核苷酸的酪蛋白激酶,它使用Mg2+或Mn2+作为二价阳离子,但在Mg2+存在下,随着NaCl浓度的增加而受到抑制,在Mn2+存在下,在50 mM NaCl时具有最佳活性。在Mg2+中,NIII仅使用ATP作为磷酸供体,但在Mn2+中,NIII从ATP或GTP转移磷酸。NIII使酪蛋白的丝氨酸和苏氨酸残基磷酸化,但不使卵黄高磷蛋白或小牛胸腺组蛋白磷酸化。