Farrell P J, Hunt T, Jackson R J
Eur J Biochem. 1978 Sep 1;89(2):517-21. doi: 10.1111/j.1432-1033.1978.tb12556.x.
We describe a method for examining the state of phosphorylation of initiation factor eIF-2 in reticulocyte lysates. The procedure involves incubation of the lysate with iodo[1-14C]acetate in 8.5 M urea, and fractionation of the labelled proteins by two-dimensional acrylamide gel electrophoresis. This approach has been used to show that haem deficiency, double-stranded RNA, and oxidised glutathione, which all inhibit the initiation of protein synthesis in an analogous manner, all cause a net increase in the level of phosphorylated eIF-2 in the complete lysate protein synthesis system.
我们描述了一种检测网织红细胞裂解物中起始因子eIF-2磷酸化状态的方法。该过程包括在8.5M尿素中用碘代[1-¹⁴C]乙酸盐孵育裂解物,并通过二维丙烯酰胺凝胶电泳对标记的蛋白质进行分级分离。这种方法已被用于表明,血红素缺乏、双链RNA和氧化型谷胱甘肽,它们都以类似的方式抑制蛋白质合成的起始,在完整的裂解物蛋白质合成系统中都会导致磷酸化eIF-2水平的净增加。