Sequence and structure space of RNA-binding peptides

被引:25
作者
Das, C [1 ]
Frankel, AD [1 ]
机构
[1] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94143 USA
关键词
RNA-binding peptides; combinatorial library; sequence specificity; MAJOR GROOVE; PHAGE DISPLAY; BACTERIOPHAGE-LAMBDA; TAT PEPTIDE; ALPHA-HELIX; RECOGNITION; SELECTION; COMPLEX; DESIGN; ANTITERMINATION;
D O I
10.1002/bip.10429
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
Studies of RNA-binding peptides, and recent combinatorial library experiments in particular, have demonstrated that diverse peptide sequences and structures can be used to recognize specific RNA sites. The identification of large numbers of sequences capable of binding to a particular site has provided extensive phylogenetic information used to deduce basic principles of recognition. The high frequency at which RNA-binding peptides are found in large sequence libraries suggests plausible routes to evolve sequence-specific binders, facilitating the design of new binding molecules and perhaps reflecting characteristics of natural evolution. (C) 2003 Wiley Periodicals, Inc.
引用
收藏
页码:80 / 85
页数:6
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