Rowlands A G, Panniers R, Henshaw E C
University of Rochester Cancer Center, New York 14642.
J Biol Chem. 1988 Apr 25;263(12):5526-33.
Guanine nucleotide exchange factor (GEF) is a multisubunit protein involved in the initiation of translation. Although numerous models have been proposed for its mechanism of action, none have been definitive. An assay dependent on GEF activity was developed using highly purified eukaryotic initiation factor 2 (eIF-2) and GEF from Ehrlich cells. GEF was considered in terms of an enzyme whose catalytic function was the exchange of eIF-2-bound [alpha-32P]GDP for unlabeled nucleotide. The turnover number of GEF at 37 degrees C, calculated on the basis of enzyme kinetic methods is 0.027 s, which is consistent with in vivo rates of protein synthesis. Moreover, kinetic data support an enzyme-substituted mechanism as the mode of GEF function. This mechanism proposes the existence of a GEF.eIF-2.GDP complex and excludes the possibility of two guanine nucleotide binding sites on eIF-2. An analogous mechanism has been recently reported for elongation factor Ts, suggesting the importance of this mechanism to protein synthesis. The mechanism of inhibition of GEF function by eIF-2 alpha phosphorylation has also been investigated. It has been generally assumed that the mechanism by which eIF-2(P) traps GEF is an excessively stable complex, from which GEF is released very slowly. Data presented here, however, reveal that eIF-2(P).GDP is a competitive inhibitor of GEF (rather than an irreversible inhibitor) competing with eIF-2.GDP for binding to GEF. Even though the eIF-2(P).GDP.GEF complex dissociates too rapidly to measure, GEF is trapped because it has at least 150-fold greater affinity for eIF-2(P).GDP than for eIF-2.GDP. The implications of competitive inhibition with respect to the mechanism of reversal of inhibition by an eIF-2(P) phosphatase are discussed.
鸟嘌呤核苷酸交换因子(GEF)是一种参与翻译起始的多亚基蛋白。尽管已经提出了许多关于其作用机制的模型,但尚无定论。利用高度纯化的真核起始因子2(eIF-2)和艾氏腹水癌细胞的GEF,开发了一种依赖于GEF活性的检测方法。GEF被视为一种酶,其催化功能是将与eIF-2结合的[α-32P]GDP与未标记的核苷酸进行交换。根据酶动力学方法计算,GEF在37℃时的转换数为0.027 s-1,这与体内蛋白质合成速率一致。此外,动力学数据支持酶替代机制作为GEF的功能模式。该机制提出存在GEF.eIF-2.GDP复合物,并排除了eIF-2上存在两个鸟嘌呤核苷酸结合位点的可能性。最近报道了延伸因子Ts的类似机制,表明该机制对蛋白质合成的重要性。还研究了eIF-2α磷酸化对GEF功能的抑制机制。一般认为,eIF-2(P)捕获GEF的机制是形成一种极其稳定的复合物,GEF从中释放非常缓慢。然而,此处给出的数据表明,eIF-2(P).GDP是GEF的竞争性抑制剂(而非不可逆抑制剂),它与eIF-2.GDP竞争结合GEF。尽管eIF-2(P).GDP.GEF复合物解离太快无法测量,但GEF被捕获是因为它对eIF-2(P).GDP的亲和力比对eIF-2.GDP至少高150倍。讨论了竞争性抑制对于eIF-2(P)磷酸酶逆转抑制机制的意义。