Successful identification of novel agents to control infectious diseases from screening mixture-based peptide combinatorial libraries in complex cell-based bioassays

被引:12
|
作者
Boggiano, C
Reixach, N
Pinilla, C
Blondelle, SE
机构
[1] Torrey Pines Inst Mol Studiess, San Diego, CA 92121 USA
[2] Mixture Sci Inc, San Diego, CA 92121 USA
关键词
antimicrobial peptides; cytotoxic T-lymphocyte vaccines; human immunodeficiency virus 1 antagonists; peptide synthetic combinatorial libraries;
D O I
10.1002/bip.10398
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
Mixture-based peptide synthetic combinatorial libraries (SCLs) represent a valuable source for the development of novel agents to control infectious diseases. Indeed, a number of studies have now proven the ability of identifying active peptides from libraries composed of thousands to millions of peptides in cell-based biosystems of varying complexity. Furthermore, progressing knowledge on the importance of endogenous peptides in various immune responses lead to a regain in importance for peptides as potential therapeutic agents. This article is aimed at providing recent studies in our laboratory for the development of antimicrobial or antiviral peptides derived from mixture-based SCLs using cell-based assays, as well as a short review of the importance of such peptides in the control of infectious diseases. Furthermore, the use of positional scanning (PS) SCL-based biometrical analyses for the identification of native optimal epitopes specific to HIV-1 proteins is also presented. (C) 2003 Wiley Periodicals, Inc.
引用
收藏
页码:103 / 116
页数:14
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