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Fluctuations between multiple EF-G-induced chimeric tRNA states during translocation on the ribosome

机译:核糖体易位期间多个EF-G诱导的嵌合tRNA状态之间的波动

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摘要

The coupled translocation of transfer RNA and messenger RNA through the ribosome entails large-scale structural rearrangements, including step-wise movements of the tRNAs. Recent structural work has visualized intermediates of translocation induced by elongation factor G (EF-G) with tRNAs trapped in chimeric states with respect to 30S and 50S ribosomal subunits. The functional role of the chimeric states is not known. Here we follow the formation of translocation intermediates by single-molecule fluorescence resonance energy transfer. Using EF-G mutants, a non-hydrolysable GTP analogue, and fusidic acid, we interfere with either translocation or EF-G release from the ribosome and identify several rapidly interconverting chimeric tRNA states on the reaction pathway. EF-G engagement prevents backward transitions early in translocation and increases the fraction of ribosomes that rapidly fluctuate between hybrid, chimeric and posttranslocation states. Thus, the engagement of EF-G alters the energetics of translocation towards a flat energy landscape, thereby promoting forward tRNA movement.
机译:通过核糖体的转移RNA和信使RNA的耦合易位需要大规模的结构重排,包括tRNA的逐步移动。最近的结构研究已经可视化了由伸长因子G(EF-G)诱导的易位中间体,其中就30S和50S核糖体亚基而言,tRNA处于嵌合状态。嵌合状态的功能作用尚不清楚。在这里,我们遵循通过单分子荧光共振能量转移的易位中间体的形成。使用EF-G突变体,不可水解的GTP类似物和夫西地酸,我们干扰核糖体的易位或EF-G释放,并在反应途径中确定了几种快速相互转化的嵌合tRNA状态。 EF-G参与阻止了易位早期的向后过渡,并增加了在杂种,嵌合和后易位状态之间快速波动的核糖体比例。因此,EF-G的参与改变了向平坦的能源格局易位的能量,从而促进了tRNA的向前运动。

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