Roy R, Nasrin N, Ahmad M F, Gupta N K
Biochem Biophys Res Commun. 1984 Aug 16;122(3):1418-25. doi: 10.1016/0006-291x(84)91249-x.
Under standard conditions, in the presence of GTP, highly purified eIF-2 and Co-eIF-2 factor preparations efficiently stimulated AUG-codon dependent but not physiological mRNA-dependent Met-tRNAf binding to 40S ribosomes. Replacement of GTP by a nonhydrolyzable GTP analog, GMP-PNP, in the above system, gave significant stimulation of Met-tRNAf binding to 40S ribosomes dependent on physiological mRNAs. Lower but significant stimulation of Met-tRNAf binding to 40S ribosomes was also observed when GTP was used in the presence of nucleoside 5'-diphosphate kinase (NDK) and ATP. ATP alone in the absence of NDK had no significant effect. This is the first report on the formation of a stable Met-tRNAf . 40S initiation complex dependent on physiological mRNAs and the factor requirements for such complex formation.
在标准条件下,在鸟苷三磷酸(GTP)存在的情况下,高度纯化的真核起始因子2(eIF-2)和协同真核起始因子2(Co-eIF-2)因子制剂能有效刺激依赖AUG密码子而非依赖生理mRNA的甲硫氨酰-tRNAf(Met-tRNAf)与40S核糖体结合。在上述系统中,用不可水解的GTP类似物鸟苷5'-三磷酸-亚甲基二磷酸(GMP-PNP)替代GTP,能显著刺激依赖生理mRNA的Met-tRNAf与40S核糖体结合。当在核苷5'-二磷酸激酶(NDK)和三磷酸腺苷(ATP)存在的情况下使用GTP时,也观察到Met-tRNAf与40S核糖体结合受到较低但显著的刺激。在没有NDK的情况下,单独的ATP没有显著影响。这是关于依赖生理mRNA形成稳定的Met-tRNAf·40S起始复合物以及这种复合物形成所需因子的首次报道。