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利用转运RNA之间的连接来实现早期肽合成。

The use of bonding between tRNAs to implement early peptide synthesis.

作者信息

Wood P N

出版信息

J Mol Evol. 1991 Nov;33(5):464-9. doi: 10.1007/BF02103139.

Abstract

Continuation of early evolutionary bonding between tRNAs would provide a solution to residence time problems between peptidyl-tRNA and mRNA. It could also improve the speed of peptide bond formation by holding the amino acid close to the growing peptide. The tRNA clover leaf structure would allow each tRNA to form a T psi C(GA)-loop bond to one side and a D-loop bond to the other, hence fixing itself within a group of tRNAs, all attached to the mRNA. This can be developed into a system for peptide elongation in which bonds are made and broken in an ordered sequence, with each step triggering the next. This leads to a model system that fits with some recent proposals for a three-site ribosome.

摘要

tRNA之间早期进化结合的延续将为肽基-tRNA和mRNA之间的停留时间问题提供解决方案。它还可以通过使氨基酸靠近正在生长的肽来提高肽键形成的速度。tRNA的三叶草叶结构将允许每个tRNA在一侧形成TψC(GA)-环键,在另一侧形成D-环键,从而将自身固定在一组都附着于mRNA的tRNA中。这可以发展成一种肽链延伸系统,其中键按有序序列形成和断裂,每一步都触发下一步。这导致了一个与最近一些关于三位点核糖体的提议相符合的模型系统。

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