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抗生素通过肽基转移酶腔抑制tRNA底物的移动。

Antibiotic inhibition of the movement of tRNA substrates through a peptidyl transferase cavity.

作者信息

Porse B T, Rodriguez-Fonseca C, Leviev I, Garrett R A

机构信息

Institute of Molecular Biology, University of Copenhagen, Denmark.

出版信息

Biochem Cell Biol. 1995 Nov-Dec;73(11-12):877-85. doi: 10.1139/o95-095.

Abstract

The present review attempts to deal with movement of tRNA substrates through the peptidyl transferase centre on the large ribosomal subunit and to explain how this movement is interrupted by antibiotics. It builds on the concept of hybrid tRNA states forming on ribosomes and on the observed movement of the 5' end of P-site-bound tRNA relative to the ribosome that occurs on peptide bond formation. The 3' ends of the tRNAs enter, and move through, a catalytic cavity where antibiotics are considered to act by at least three primary mechanisms: (i) they interfere with the entry of the aminoacyl moiety into the catalytic cavity before peptide bond formation; (ii) they inhibit movement of the nascent peptide along the peptide channel, a process that may generally involve destabilization of the peptidyl tRNA, and (iii) they prevent movement of the newly deacylated tRNA between the P/P and hybrid P/E sites on peptide bond formation.

摘要

本综述试图探讨tRNA底物在大核糖体亚基上通过肽基转移酶中心的移动情况,并解释这种移动是如何被抗生素阻断的。它基于核糖体上形成的杂合tRNA状态的概念,以及在肽键形成时P位点结合的tRNA的5'端相对于核糖体的观察到的移动。tRNA的3'端进入并穿过一个催化腔,抗生素被认为至少通过三种主要机制在该腔内起作用:(i)它们在肽键形成前干扰氨酰基部分进入催化腔;(ii)它们抑制新生肽沿着肽通道的移动,这一过程通常可能涉及肽基tRNA的不稳定;(iii)它们在肽键形成时阻止新脱酰基的tRNA在P/P和杂合P/E位点之间移动。

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