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鉴定16S rRNA中对于tRNA在30S核糖体P位点结合至关重要的碱基。

Identification of bases in 16S rRNA essential for tRNA binding at the 30S ribosomal P site.

作者信息

von Ahsen U, Noller H F

机构信息

Sinsheimer Laboratories, University of California, Santa Cruz 95064.

出版信息

Science. 1995 Jan 13;267(5195):234-7. doi: 10.1126/science.7528943.

Abstract

Previous studies suggest that the mechanism of action of the ribosome in translation involves crucial transfer RNA (tRNA)-ribosomal RNA (rRNA) interactions. Here, a selection scheme was developed to identify bases in 16S rRNA that are essential for tRNA binding to the P site of the small (30S) ribosomal subunit. Modification of the N-1 and N-2 positions of 2-methylguanine 966 and of the N-7 position of guanine 1401 interfered with messenger RNA (mRNA)-dependent binding of tRNA to the P site. Modification of the same positions as well as of the N-1 and N-2 positions of guanine 926 interfered with mRNA-independent binding of tRNA at high magnesium ion concentration. These results suggest that these three bases are involved in intermolecular contacts between ribosomes and tRNA.

摘要

先前的研究表明,核糖体在翻译过程中的作用机制涉及关键的转运RNA(tRNA)-核糖体RNA(rRNA)相互作用。在此,开发了一种筛选方案,以鉴定16S rRNA中对于tRNA结合小(30S)核糖体亚基的P位点至关重要的碱基。2-甲基鸟嘌呤966的N-1和N-2位置以及鸟嘌呤1401的N-7位置的修饰干扰了tRNA与P位点的信使RNA(mRNA)依赖性结合。相同位置以及鸟嘌呤926的N-1和N-2位置的修饰在高镁离子浓度下干扰了tRNA的mRNA非依赖性结合。这些结果表明,这三个碱基参与了核糖体与tRNA之间的分子间接触。

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