Matts R L, Thomas N S, Hurst R, London I M
Department of Biochemistry, Oklahoma State University, Stillwater 74078.
FEBS Lett. 1988 Aug 15;236(1):179-84. doi: 10.1016/0014-5793(88)80310-7.
The recycling of eukaryotic initiation factor eIF-2 requires the exchange of GDP for GTP, in a reaction catalyzed by the reversing factor (RF). Recent studies have suggested that a 60 S ribosomal subunit-bound eIF-2.GDP complex is an intermediate in protein chain initiation. We have monitored the distribution of RF in heme-deficient and dsRNA-inhibited lysates by immunoblot analysis of sucrose gradient fractions and have compared the distribution with that of eIF-2(alpha-32P). RF and eIF-2(alpha P) were both found to be tightly associated with 60 S and 80 S ribosomes, as their distribution did not change in gradients containing up to 0.1 M K+. The association of eIF-2(alpha-32P) and RF with 60 S and 80 S ribosomes was enhanced in the presence of F-, indicating the presence of an endogenous ribosome-associated phosphatase activity which is capable of dephosphorylating eIF-2(alpha P) in the absence of F-. These observations are consistent with the hypothesis that under physiologic conditions, RF interacts with the 60 S-bound eIF-2.GDP complex to promote the dissociation of GDP from eIF-2 and the release of eIF-2 from the 60 S subunit as a complex with RF.
真核生物起始因子eIF-2的再循环需要在逆转因子(RF)催化的反应中将GDP置换为GTP。最近的研究表明,与60S核糖体亚基结合的eIF-2.GDP复合物是蛋白质链起始过程中的一个中间体。我们通过对蔗糖梯度分级分离物进行免疫印迹分析,监测了血红素缺乏和双链RNA抑制裂解物中RF的分布,并将其分布与eIF-2(α-32P)的分布进行了比较。发现RF和eIF-2(αP)都与60S和80S核糖体紧密相关,因为在含有高达0.1M K+的梯度中它们的分布没有变化。在F-存在的情况下,eIF-2(α-32P)和RF与60S和80S核糖体的结合增强,这表明存在一种内源性核糖体相关磷酸酶活性,其能够在没有F-的情况下使eIF-2(αP)去磷酸化。这些观察结果与以下假设一致:在生理条件下,RF与60S结合的eIF-2.GDP复合物相互作用,以促进GDP从eIF-2上解离,并使eIF-2作为与RF的复合物从60S亚基上释放。