Engineering RNA-binding proteins for biology

被引:77
作者
Chen, Yu
Varani, Gabriele [1 ]
机构
[1] Univ Washington, Dept Biochem, Seattle, WA 98195 USA
关键词
computational design; in vitro evolution; phage display; protein engineering; protein-RNA interactions; RNA recognition motif; RNA-binding domains; RNA-binding proteins; yeast three-hybrid system; zinc finger; ZINC-FINGER DOMAIN; SINGLE-STRANDED RNA; AU-RICH-ELEMENT; CELL-FREE SELECTION; STRUCTURAL BASIS; CRYSTAL-STRUCTURE; MOLECULAR-BASIS; REPEAT PROTEINS; DNA RECOGNITION; HUMAN PUMILIO;
D O I
10.1111/febs.12375
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
RNA-binding proteins play essential roles in the regulation of gene expression. Many have modular structures and combine relatively few common domains in various arrangements to recognize RNA sequences and/or structures. Recent progress in engineering the specificity of the PUF class RNA-binding proteins has shown that RNA-binding domains may be combined with various effector or functional domains to regulate the metabolism of targeted RNAs. Designer RNA-binding proteins with tailored sequence specificity will provide valuable tools for biochemical research as well as potential therapeutic applications. In this review, we discuss the suitability of various RNA-binding domains for engineering RNA-binding specificity, based on the structural basis for their recognition. We also compare various protein engineering and design methods applied to RNA-binding proteins, and discuss future applications of these proteins.
引用
收藏
页码:3734 / 3754
页数:21
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