Woodley C L, Roychowdhury M, MacRae T H, Olsen K W, Wahba A J
Eur J Biochem. 1981 Jul;117(3):543-51.
We have purified from the ribosomal wash of dormant and developing embryos of Artemia two proteins, Co-eIF-2(A) and Co-eIF-2(B). These factors are essential for ternary complex formation and binding of [35S]-Met-tRNAf to 40-S ribosomal subunits with 15-30 microgram eIF-2/ml of reaction mixture. On polyacrylamide gel electrophoresis in dodecylsulfate, Co-eIF-2(A) is composed of a single polypeptide of Mr 65 000, whereas Co-eIF-2(B) contains polypeptides of Mr 105000 and 112000. Co-eIF-2(A) is sensitive to 4.5 microM aurintricarboxylic acid but Co-eIF-2(B) requires approximately 15 microM aurintricarboxylic acid to give 50% inhibition of ternary complex formation. The stimulatory activity of both factors is abolished by pretreatment of the proteins with N-ethylmaleimide. Artemia eIF-2 rapidly bonds [3H]GDP or [3H]GTP and at 15 degrees C the initiation factor rapidly equilibrates bound nucleotides with free GDP or GTP. Both Co-eIF-2(A) and Co-eIF-2(B) have no effect on the exchange or the amount of nucleotide bound. The small subunit (Mr 43 000) of Artemia eIF-2 is phosphorylated in the presence of the rabbit reticulocyte heme-repressible kinase. Tryptic digestion of [32P]phosphorylated eIF-2 produces a single major phosphopeptide and several minor ones. Acid hydrolysis of these phosphopeptides, as well as of [32P]phosphorylated eIF-2, demonstrates that the radioactivity is predominantly associated with phosphoserine. Phosphorylated Artemia eIF-2 is active in ternary complex formation, in AUG-dependent binding of [35S]Met-tRNAf to 40-S ribosomal subunits and in cell-free protein synthesis. Both Co-eIF-2(A) and Co-eIF-2(B) stimulate ternary complex formation with phosphorylated eIF-2. A kinase that phosphorylates the small subunit of eIF-2 is present in the post-ribosomal supernatant as well as in the ribosomal wash of developing Artemia embryos.
我们从卤虫休眠和发育胚胎的核糖体洗脱液中纯化出了两种蛋白质,即协同真核起始因子2(A)(Co-eIF-2(A))和协同真核起始因子2(B)(Co-eIF-2(B))。这些因子对于三元复合物的形成以及在反应混合物中每毫升含15 - 30微克真核起始因子2(eIF-2)时[35S]-甲硫氨酰 - 起始tRNA([35S]-Met-tRNAf)与40S核糖体亚基的结合至关重要。在十二烷基硫酸盐聚丙烯酰胺凝胶电泳中,Co-eIF-2(A)由一条分子量为65000的单一多肽组成,而Co-eIF-2(B)包含分子量为105000和112000的多肽。Co-eIF-2(A)对4.5微摩尔金精三羧酸敏感,但Co-eIF-2(B)需要约15微摩尔金精三羧酸才能使三元复合物形成受到50%的抑制。用N - 乙基马来酰亚胺预处理这些蛋白质会消除这两种因子的刺激活性。卤虫eIF-2能快速结合[3H]GDP或[3H]GTP,在15℃时,这种起始因子能使结合的核苷酸与游离的GDP或GTP迅速达到平衡。Co-eIF-2(A)和Co-eIF-2(B)对核苷酸的交换或结合量均无影响。卤虫eIF-2的小亚基(分子量43000)在兔网织红细胞血红素可抑制激酶存在的情况下会发生磷酸化。对[32P]磷酸化的eIF-2进行胰蛋白酶消化会产生一个主要的磷酸肽和几个次要的磷酸肽。这些磷酸肽以及[32P]磷酸化的eIF-2经酸水解表明,放射性主要与磷酸丝氨酸相关。磷酸化的卤虫eIF-2在三元复合物形成、[35S]Met-tRNAf在AUG依赖下与40S核糖体亚基的结合以及无细胞蛋白质合成中均具有活性。Co-eIF-2(A)和Co-eIF-2(B)都能刺激磷酸化的eIF-2形成三元复合物。一种使eIF-2小亚基磷酸化的激酶存在于发育中的卤虫胚胎的核糖体后上清液以及核糖体洗脱液中。