Synthetic peptide arrays and peptide combinatorial libraries for the exploration of protein-ligand interactions and the design of protein inhibitors

被引:25
作者
Eichler, J [1 ]
机构
[1] German Res Ctr Biotechnol, GBF, D-38124 Braunschweig, Germany
关键词
D O I
10.2174/1386207053258497
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Synthetic peptides have a long tradition as molecular tools in biomedical research and drug discovery. The introduction of high-throughput synthesis and screening technologies for synthetic peptides, such as arrays and combinatorial libraries, enabled the large-scale and detailed exploration of protein-ligand interactions, as well as the discovery of novel biologically active peptides. This review summarizes currently available synthetic peptide array and library technologies, in particular mixture-based peptide libraries, which are illustrated by numerous applications in various fields of biomedical research.
引用
收藏
页码:135 / 143
页数:9
相关论文
共 116 条
[1]   Identification of inhibitors of prohormone convertases 1 and 2 using a peptide combinatorial library [J].
Apletalina, E ;
Appel, J ;
Lamango, NS ;
Houghten, RA ;
Lindberg, I .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (41) :26589-26595
[2]  
Appel JR, 1998, J PEPT RES, V52, P346
[3]   Synthesis of positional-scanning libraries of fluorogenic peptide substrates to define the extended substrate specificity of plasmin and thrombin [J].
Backes, BJ ;
Harris, JL ;
Leonetti, F ;
Craik, CS ;
Ellman, JA .
NATURE BIOTECHNOLOGY, 2000, 18 (02) :187-193
[4]   Discovery of alpha-1-proteinase inhibitor binding peptides from the screening of a solid phase combinatorial peptide library [J].
Bastek, PD ;
Land, JM ;
Baumbach, GA ;
Hammond, DH ;
Carbonell, RG .
SEPARATION SCIENCE AND TECHNOLOGY, 2000, 35 (11) :1681-1706
[5]   A linear hexapeptide somatostatin antagonist blocks somatostatin activity in vitro and influences growth hormone release in rats [J].
Baumbach, WR ;
Carrick, TA ;
Pausch, MH ;
Bingham, B ;
Carmignac, D ;
Robinson, ICAF ;
Houghten, R ;
Eppler, CM ;
Price, LA ;
Zysk, JR .
MOLECULAR PHARMACOLOGY, 1998, 54 (05) :864-873
[6]   Epitope-targeted proteome analysis: towards a large-scale automated protein-protein-interaction mapping utilizing synthetic peptide arrays [J].
Bialek, K ;
Swistowski, A ;
Frank, R .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2003, 376 (07) :1006-1013
[7]  
Blondelle SE, 2003, METHOD ENZYMOL, V369, P322
[8]   IDENTIFICATION OF ANTIMICROBIAL PEPTIDES BY USING COMBINATORIAL LIBRARIES MADE UP OF UNNATURAL AMINO-ACIDS [J].
BLONDELLE, SE ;
TAKAHASHI, E ;
WEBER, PA ;
HOUGHTEN, RA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1994, 38 (10) :2280-2286
[9]   Novel, potent calmodulin antagonists derived from an all-D hexapeptide combinatorial library that inhibit in vivo cell proliferation:: activity and structural characterization [J].
Blondelle, SE ;
Crooks, E ;
Aligué, R ;
Agell, N ;
Bachs, O ;
Esteve, V ;
Tejero, R ;
Celda, B ;
Pastor, MT ;
Pérez-Payá, E .
JOURNAL OF PEPTIDE RESEARCH, 2000, 55 (02) :148-162
[10]  
Blondelle SE, 1996, J BIOL CHEM, V271, P4093, DOI 10.1074/jbc.271.8.4093