【2h】

A recent intermezzo at the Ribosome Club

机译:核糖体俱乐部最近的间奏曲

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摘要

Two sets of ribosome structures have recently led to two different interpretations of what limits the accuracy of codon translation by transfer RNAs. In this review, inspired by this intermezzo at the Ribosome Club, we briefly discuss accuracy amplification by energy driven proofreading and its implementation in genetic code translation. We further discuss general ways by which the monitoring bases of 16S rRNA may enhance the ultimate accuracy (d-values) and how the codon translation accuracy is reduced by the actions of Mg2+ ions and the presence of error inducing aminoglycoside antibiotics. We demonstrate that complete freezing-in of cognate-like tautomeric states of ribosome-bound nucleotide bases in transfer RNA or messenger RNA is not compatible with recent experiments on initial codon selection by transfer RNA in ternary complex with elongation factor Tu and GTP. From these considerations, we suggest that the sets of 30S subunit structures from the Ramakrishnan group and 70S structures from the Yusupov/Yusupova group may, after all, reflect two sides of the same coin and how the structurally based intermezzo at the Ribosome Club may be resolved simply by taking the dynamic aspects of ribosome function into account.This article is part of the themed issue ‘Perspectives on the ribosome’.
机译:两组核糖体结构最近导致了对转移RNA限制密码子翻译准确性的两种不同解释。在这篇评论中,受核糖体俱乐部间奏曲的启发,我们简要讨论了能量驱动校对的准确性放大及其在遗传密码翻译中的实现。我们进一步讨论了16S rRNA的监测碱基可以提高最终准确性(d值)的一般方法,以及Mg 2 + 离子的作用和存在Mg 会如何降低密码子翻译的准确性。错误诱导氨基糖苷类抗生素。我们证明转移RNA或信使RNA中的核糖体结合核苷酸碱基的同源样互变异构状态的完全冻结与在伸长因子Tu和GTP的三元复合物中通过转移RNA进行初始密码子选择的最新实验不兼容。基于这些考虑,我们建议,Ramakrishnan组的30S亚基结构和Yusupov / Yusupova组的70S结构的集合毕竟可能反映同一枚硬币的两个侧面,以及核糖体俱乐部的基于结构的中间基可能是只需考虑核糖体功能的动态方面即可解决。本文是主题“核糖体的观点”的一部分。

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