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蛋白质-RNA识别

Protein-RNA recognition.

作者信息

Draper D E

机构信息

Department of Chemistry, Johns Hopkins University, Baltimore, Maryland 21218, USA.

出版信息

Annu Rev Biochem. 1995;64:593-620. doi: 10.1146/annurev.bi.64.070195.003113.

Abstract

Specific interactions between RNAs and proteins are fundamental to many cellular processes, including the assembly and function of ribonucleoprotein particles (RNPs), such as ribosomes and spliceosomes and the post-transcriptional regulation of gene expression. Among the complexes studied to date are small RNAs bound to individual amino acids, tRNAs and tRNA fragments bound to their cognate aminoacyl-tRNA synthetases, and a variety of proteins bound to RNA single strands, hairpins, irregular helices, and tertiary structures stabilized by bound cations. Several proteins use a beta-sheet surface to bind RNAs, and others insert an alpha-helix into the widened major groove of a non-canonical RNA helix. Distortion or rearrangement of the RNA structure by bound protein is a common theme. The structural details of protein-RNA complexes are being resolved by nuclear magnetic resonance (NMR) and X-ray crystallography, but thorough thermodynamic analyses of recognition mechanisms have yet to be performed.

摘要

RNA与蛋白质之间的特异性相互作用是许多细胞过程的基础,包括核糖核蛋白颗粒(RNP)的组装和功能,如核糖体和剪接体,以及基因表达的转录后调控。迄今为止研究的复合物包括与单个氨基酸结合的小RNA、与其同源氨酰-tRNA合成酶结合的tRNA和tRNA片段,以及与RNA单链、发夹、不规则螺旋和由结合阳离子稳定的三级结构结合的多种蛋白质。几种蛋白质利用β-折叠表面结合RNA,其他蛋白质则将α-螺旋插入非经典RNA螺旋变宽的大沟中。结合蛋白导致RNA结构的扭曲或重排是一个常见的现象。蛋白质-RNA复合物的结构细节正在通过核磁共振(NMR)和X射线晶体学解析,但对识别机制的全面热力学分析尚未进行。

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