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解码错误与E位点的参与。

Decoding errors and the involvement of the E-site.

作者信息

Nierhaus Knud H

机构信息

Max-Planck-Institut für Molekulare Genetik, Ihnestrasse 73, AG Ribosomen, D-14195 Berlin, Germany.

出版信息

Biochimie. 2006 Aug;88(8):1013-9. doi: 10.1016/j.biochi.2006.02.009. Epub 2006 Mar 23.

Abstract

Life depends on the faithful translation of the genetic information into proteins. Ribosomes have developed remarkable mechanisms to ensure the accurate synthesis of proteins. In the first part of this review various types of ribosomal errors and their importance for cell-life are surveyed, while in the second part two important aspects of the ribosomal E-site for the accuracy of translation are considered: (i) The fact that usually misincorporations are not harmful for the cell, since only one in about 400 misincorporations will affect the structure and/or function of a protein, is a function of the E-site. (ii) In contrast, an extremely harmful translational error is a loss of the reading frame, resulting in an immediate loss of the genetic information. Maintenance of the reading frame is one of the most remarkable achievements of the ribosome; only once in about 30,000 elongation cycles is the reading frame lost. A cognate tRNA at the E-site is an essential prerequisite for this high precision.

摘要

生命依赖于将遗传信息准确地翻译为蛋白质。核糖体已经进化出了非凡的机制来确保蛋白质的精确合成。在本综述的第一部分,我们探讨了各种类型的核糖体错误及其对细胞生命的重要性,而在第二部分,我们考虑了核糖体E位点对翻译准确性的两个重要方面:(i)通常错误掺入对细胞无害,因为大约每400次错误掺入中只有一次会影响蛋白质的结构和/或功能,这是E位点的功能。(ii)相反,一种极其有害的翻译错误是阅读框的丢失,这会导致遗传信息立即丧失。维持阅读框是核糖体最显著的成就之一;大约每30000次延伸循环中才会有一次阅读框丢失。E位点上的同源tRNA是实现这种高精度的必要前提。

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