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RNA结合肽的序列和结构空间

Sequence and structure space of RNA-binding peptides.

作者信息

Das Chandreyee, Frankel Alan D

机构信息

Department of Biochemistry and Biophysics, 600 16th Street University of California, San Francisco, CA 94143-2280, USA.

出版信息

Biopolymers. 2003 Sep;70(1):80-5. doi: 10.1002/bip.10429.

Abstract

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.

摘要

对RNA结合肽的研究,尤其是最近的组合文库实验,已经证明了多种肽序列和结构可用于识别特定的RNA位点。大量能够结合特定位点的序列的鉴定提供了广泛的系统发育信息,用于推导识别的基本原理。在大型序列文库中发现RNA结合肽的高频率表明了进化序列特异性结合剂的合理途径,有助于设计新的结合分子,也许还反映了自然进化的特征。

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