Dahl H H, Truelsen E, Blair G E
Eur J Biochem. 1977 Jul 1;77(1):209-16. doi: 10.1111/j.1432-1033.1977.tb11659.x.
A fractionated cell-free protein-synthesising system from Krebs II ascites tumour cells is described. It is dependent on the addition of exogenous mRNA. In this system the translation of natural mRNAs requires the presence of four initiation factors: the high-molecular-weight complex IF-M3, IFEMC and two low-molecular-weight proteins IF-Malpha and IF-Mbeta. None of these factors are required for the translation of the synthetic messenger poly(A,U,G). The purification of IF-Malpha and IF-Mbeta was achieved by the use of gel and ion-exchange chromatography. Analysis of the purified proteins by sodium dodecyl sulphate/polyacrylamide gel electrophoresis showed that the molecular weight of IF-Malpha is 19,000 and that of IF-Mbeta is 15,000. The initiation factor IF-E1 isolated from rabbit reticulocytes can substitute for IF-Mbeta in the translation of encephalomyocarditis virus RNA. IF-Malpha does not correspond to any previously recognised eukaryotic initiation factor.
本文描述了一种来自克雷布斯II腹水瘤细胞的分级无细胞蛋白质合成系统。该系统依赖于外源mRNA的添加。在这个系统中,天然mRNA的翻译需要四种起始因子:高分子量复合物IF-M3、IFEMC以及两种低分子量蛋白质IF-Mα和IF-Mβ。合成信使多聚(A,U,G)的翻译不需要这些因子中的任何一种。通过凝胶和离子交换色谱法实现了IF-Mα和IF-Mβ的纯化。用十二烷基硫酸钠/聚丙烯酰胺凝胶电泳对纯化后的蛋白质进行分析表明,IF-Mα的分子量为19000,IF-Mβ的分子量为15000。从兔网织红细胞中分离出的起始因子IF-E1可以在脑心肌炎病毒RNA的翻译中替代IF-Mβ。IF-Mα与任何先前公认的真核起始因子都不对应。