Redpath N T, Proud C G
Department of Biochemistry, School of Medical Sciences, University of Bristol, U.K.
Biochem J. 1990 Nov 15;272(1):175-80. doi: 10.1042/bj2720175.
The protein phosphatases active against phosphorylase a, elongation factor-2 (EF-2) and the alpha-subunit of initiation factor-2 (eIF-2) [eIF-2(alpha P)] were studied in extracts of rabbit reticulocytes. Swiss-mouse 3T3 fibroblasts and rat hepatocytes, by use of the specific phosphatase inhibitors okadaic acid and inhibitor proteins-1 and -2. In all three extracts tested, both phosphatase-1 and phosphatase-2A contributed to overall phosphatase activity against phosphorylase and eIF-2(alpha P), but phosphatase-2B and -2C did not. In contrast, only protein phosphatase-2A was active against EF-2. Furthermore, in hepatocytes there was substantial type-2C phosphatase activity against EF-2, but not against phosphorylase or eIF-2 alpha. These findings in cell extracts were borne out by data obtained by studying the activities of purified protein phosphatase-1 and -2A against eIF-2(alpha P) and eIF-2(alpha P) was a moderately good substrate for both enzymes (relative to phosphorylase a). In contrast, EF-2 was a very poor substrate for protein phosphatase-1, but was dephosphorylated faster than phosphorylase a by protein phosphatase-2A. The implications of these findings for the control of translation and their relationships to previous work are discussed.
利用特异性磷酸酶抑制剂冈田酸以及抑制蛋白 -1 和 -2,对兔网织红细胞、瑞士小鼠 3T3 成纤维细胞和大鼠肝细胞提取物中作用于磷酸化酶 a、延伸因子 -2(EF-2)和起始因子 -2 的α亚基(eIF-2)[eIF-2(αP)]的蛋白磷酸酶进行了研究。在所有测试的三种提取物中,磷酸酶 -1 和磷酸酶 -2A 均对磷酸化酶和 eIF-2(αP)的总体磷酸酶活性有贡献,但磷酸酶 -2B 和 -2C 则无此作用。相比之下,只有蛋白磷酸酶 -2A 对 EF-2 有活性。此外,在肝细胞中存在大量针对 EF-2 的 2C 型磷酸酶活性,但对磷酸化酶或 eIF-2α 则无活性。通过研究纯化的蛋白磷酸酶 -1 和 -2A 对 eIF-2(αP)的活性所获得的数据证实了细胞提取物中的这些发现,并且 eIF-2(αP)是这两种酶的中等良好底物(相对于磷酸化酶 a)。相比之下,EF-2 是蛋白磷酸酶 -1 的非常差的底物,但被蛋白磷酸酶 -2A 去磷酸化的速度比磷酸化酶 a 快。讨论了这些发现对翻译控制的意义及其与先前工作的关系。