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共翻译折叠途径中的思考停顿。

A pause for thought along the co-translational folding pathway.

作者信息

Komar Anton A

机构信息

Department of Biological, Center for Gene Regulation in Health and Disease, Cleveland State University, Cleveland, OH 44115, USA.

出版信息

Trends Biochem Sci. 2009 Jan;34(1):16-24. doi: 10.1016/j.tibs.2008.10.002. Epub 2008 Nov 6.

Abstract

A unifying concept that combines the basic features governing self-organization of proteins into complex three-dimensional structures in vitro and in vivo is still lacking. Recent experimental results and theoretical in silico modeling studies provide evidence showing that mRNA might contain an additional layer of information, beyond the amino acid sequence, that fine-tunes in vivo protein folding, which is largely believed to start as a co-translational process. These findings indicate that translation kinetics might direct the co-translational folding pathway and that translational pausing at rare codons might provide a time delay to enable independent and sequential folding of the defined portions of the nascent polypeptide emerging from the ribosome.

摘要

目前仍缺乏一个统一的概念,来整合在体外和体内将蛋白质自组装成复杂三维结构的基本特征。最近的实验结果和计算机模拟理论研究提供了证据,表明信使核糖核酸(mRNA)可能包含氨基酸序列之外的另一层信息,这层信息可微调体内蛋白质折叠,而人们普遍认为蛋白质折叠主要是一个共翻译过程。这些发现表明,翻译动力学可能指导共翻译折叠途径,并且在稀有密码子处的翻译暂停可能提供一个时间延迟,以使从核糖体中出现的新生多肽的特定部分能够独立且有序地折叠。

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