组合化学
肽
药物发现
鉴定(生物学)
计算生物学
单克隆抗体
化学
药物开发
计算机科学
肽库
药品
组合综合
肽合成
生物
生物化学
肽序列
抗体
遗传学
药理学
基因
植物
作者
Richard A. Houghten,Clemencia Pinilla,Sylvie E. Blondelle,Jon R. Appel,Colette T. Dooley,Julio H. Cuervo
出处
期刊:Nature
[Springer Nature]
日期:1991-11-01
卷期号:354 (6348): 84-86
被引量:1274
摘要
Existing methods for the synthesis and screening of large numbers of peptides are limited by their inability to generate and screen the requisite number (millions) of individual peptides and/or their inability to generate unmodified free peptides in quantities able to interact in solution. We have circumvented these limitations by developing synthetic peptide combinatorial libraries composed of mixtures of free peptides in quantities which can be used directly in virtually all existing assay systems. The screening of these heterogeneous libraries, along with an iterative selection and synthesis process, permits the systematic identification of optimal peptide ligands. Starting with a library composed of more than 34 million hexa-peptides, we present here the precise identification of an antigenic determinant recognized by a monoclonal antibody as well as the straightforward development of new potent antimicrobial peptides.
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