Manchester K L
Department of Biochemistry, University of the Witwatersrand, Johannesburg, South Africa.
Biochem Biophys Res Commun. 1997 Jan 3;230(1):27-9. doi: 10.1006/bbrc.1996.5804.
The findings of Parkhurst et al. (Biochemistry 33, 15168-15177:1994) that a 10-mer oligoribonucleotide containing the AUG triplet enhances the binding of the eIF-2 x Met-tRNAi complex to the 40S ribosomal subunit are questioned on the basis of a re-evaluation of their calculations. It is not possible to conclude, as they did, that addition of the AUG-containing oligonucleotide produces an exceptionally large increase (as judged by the magnitude of the coupling free energy) in the binding of the eIF-2 x Met-tRNAi complex to the 40S subunit, or that their results are more consistent with internal initiation than with the scanning initiation model.
基于对帕克赫斯特等人(《生物化学》33卷,15168 - 15177页:1994年)计算结果的重新评估,他们关于一个含有AUG三联体的10聚体寡核糖核苷酸能增强真核起始因子2(eIF - 2)与甲硫氨酰 - 起始tRNA(Met - tRNAi)复合物与40S核糖体亚基结合的研究结果受到质疑。像他们那样得出结论,即添加含AUG的寡核苷酸会使eIF - 2与Met - tRNAi复合物与40S亚基的结合产生异常大的增加(以偶联自由能的大小来判断),或者他们的结果与内部起始模型比与扫描起始模型更一致,这是不可能的。