Combinatorial peptide library methods for immunobiology research

被引:70
作者
Liu, RW
Enstrom, AM
Lam, KS
机构
[1] Univ Calif Davis, Ctr Canc, Div Hematol Oncol, Sacramento, CA 95817 USA
[2] Univ Calif Davis, Dept Internal Med, Sacramento, CA 95817 USA
关键词
D O I
10.1016/S0301-472X(02)01008-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The field of combinatorial peptide chemistry has emerged as a powerful tool in the study of many biological systems. This review focuses on combinatorial peptide library methodology, which includes biological library methods, spatially addressable parallel library methods, library methods requiring deconvolution, the "one-bead one-compound" library method, and affinity chromatography selection method. These peptide libraries have successfully been employed to study a vast array of cell surface receptors, as well as have been useful in identifying protein kinase substrates and inhibitors. In recent immunobiological applications, peptide libraries have proven monumental in the definition of MHC anchor residues, in lymphocyte epitope mapping, and in the development of peptide vaccines. Peptides identified from such libraries, when presented in a chemical microarray format, may prove useful in immunodiagnostics. Combinatorial peptide libraries offer a high-throughput approach to study limitless biological targets. Peptides discovered from such studies may be therapeutically and diagnostically useful agents. (C) 2003 International Society for Experimental Hematology. Published by Elsevier Science Inc.
引用
收藏
页码:11 / 30
页数:20
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