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细菌 30S 翻译起始复合物的实时组装图谱。

Real-time assembly landscape of bacterial 30S translation initiation complex.

机构信息

Max Planck Institute for Biophysical Chemistry, Göttingen, Germany.

出版信息

Nat Struct Mol Biol. 2012 May 6;19(6):609-15. doi: 10.1038/nsmb.2285.

Abstract

Initiation factors guide the ribosome in the selection of mRNA and translational reading frame. We determined the kinetically favored assembly pathway of the 30S preinitiation complex (30S PIC), an early intermediate in 30S initiation complex formation in Escherichia coli. IF3 and IF2 are the first factors to arrive, forming an unstable 30S-IF2-IF3 complex. Subsequently, IF1 joins and locks the factors in a kinetically stable 30S PIC to which fMet-tRNA(fMet) is recruited. Binding of mRNA is independent of initiation factors and can take place at any time during 30S PIC assembly, depending on the cellular concentration of the mRNA and the structural determinants at the ribosome-binding site. The kinetic analysis shows both specific and cumulative effects of initiation factors as well as kinetic checkpoints of mRNA selection at the entry into translation.

摘要

起始因子引导核糖体选择 mRNA 和翻译阅读框。我们确定了 30S 起始复合物(30S PIC)的动力学有利组装途径,这是大肠杆菌 30S 起始复合物形成的早期中间产物。IF3 和 IF2 是首先到达的因子,形成不稳定的 30S-IF2-IF3 复合物。随后,IF1 加入并将因子锁定在动力学稳定的 30S PIC 中,该复合物招募了 fMet-tRNA(fMet)。mRNA 的结合不依赖于起始因子,并且可以在 30S PIC 组装的任何时间进行,这取决于 mRNA 的细胞浓度和核糖体结合位点的结构决定因素。动力学分析显示了起始因子的特异性和累积效应,以及翻译起始时 mRNA 选择的动力学检查点。

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