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A recent intermezzo at the Ribosome Club

机译:核糖体俱乐部最近的Intermezzo

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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.
机译:最近,两组核糖体结构导致了对限制转移RNA密码子翻译准确性的两种不同解释。在这篇综述中,受核糖体俱乐部的这个间奏曲的启发,我们简要讨论了通过能量驱动的校对实现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的监测基础可能提高最终准确性(d值)的一般方法,以及Mg2+离子的作用和错误诱导氨基糖苷类抗生素的存在如何降低密码子翻译的准确性。我们证明,转移RNA或信使RNA中核糖体结合核苷酸碱基的同源互变异构状态的完全冻结与最近通过转移RNA与延伸因子Tu和GTP的三元复合物选择初始密码子的实验不兼容。从这些考虑,我们认为罗摩克里希南群的30S亚单位结构和尤苏波夫/尤苏波娃群的70S亚单位结构可能最终反映了同一个硬币的两面,以及如何简单地通过考虑核糖体功能的动态方面来解决核糖体俱乐部中基于结构的间奏。

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