Phage display in pharmaceutical biotechnology

被引:210
作者
Sidhu, SS [1 ]
机构
[1] Genentech Inc, Dept Prot Engn, San Francisco, CA 94080 USA
关键词
D O I
10.1016/S0958-1669(00)00152-X
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Over the past year, methods for the construction of M13 phage-display libraries have been significantly improved and new display formats have been developed. Phage-displayed peptide libraries have been used to isolate specific ligands for numerous protein targets. New phage antibody libraries have further expanded the practical applications of the technology and phage cDNA libraries have proven useful in defining natural binding interactions. In addition, phage-display methods have been developed for the rapid determination of binding energetics at protein-protein interfaces.
引用
收藏
页码:610 / 616
页数:7
相关论文
共 51 条
[1]   HORMONE PHAGE - AN ENRICHMENT METHOD FOR VARIANT PROTEINS WITH ALTERED BINDING-PROPERTIES [J].
BASS, S ;
GREENE, R ;
WELLS, JA .
PROTEINS-STRUCTURE FUNCTION AND GENETICS, 1990, 8 (04) :309-314
[2]   The crystal structure of a GroEL/peptide complex: Plasticity as a basis for substrate diversity [J].
Chen, LL ;
Sigler, PB .
CELL, 1999, 99 (07) :757-768
[3]   Selection and analysis of an optimized anti-VEGF antibody: Crystal structure of an affinity-matured Fab in complex with antigen [J].
Chen, Y ;
Wiesmann, C ;
Fuh, G ;
Li, B ;
Christinger, HW ;
McKay, P ;
de Vos, AM ;
Lowman, HB .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 293 (04) :865-881
[4]   Antagonists of protein-protein interactions [J].
Cochran, AG .
CHEMISTRY & BIOLOGY, 2000, 7 (04) :R85-R94
[5]   Identification of natural ligands for SH2 domains from a phage display cDNA library [J].
Cochrane, D ;
Webster, C ;
Masih, G ;
McCafferty, J .
JOURNAL OF MOLECULAR BIOLOGY, 2000, 297 (01) :89-97
[6]   Antibody engineering [J].
Dall'Acqua, W ;
Carter, P .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 1998, 8 (04) :443-450
[7]   Convergent solutions to binding at a protein-protein interface [J].
DeLano, WL ;
Ultsch, MH ;
de Vos, AM ;
Wells, JA .
SCIENCE, 2000, 287 (5456) :1279-1283
[8]   Peptide exosite inhibitors of factor VIIa as anticoagulants [J].
Dennis, MS ;
Eigenbrot, C ;
Skelton, NJ ;
Ultsch, MH ;
Santell, L ;
Dwyer, MA ;
O'Connell, MP ;
Lazarus, RA .
NATURE, 2000, 404 (6777) :465-470
[9]   Modified phage peptide libraries as a tool to study specificity of phosphorylation and recognition of tyrosine containing peptides [J].
Dente, L ;
Vetriani, C ;
Zucconi, A ;
Pelicci, G ;
Lanfrancone, L ;
Pelicci, PG ;
Cesareni, G .
JOURNAL OF MOLECULAR BIOLOGY, 1997, 269 (05) :694-703
[10]   Total alanine-scanning mutagenesis of insulin-like growth factor I (IGF-I) identifies differential binding epitopes for IGFBP-1 and IGFBP-3 [J].
Dubaquié, Y ;
Lowman, HB .
BIOCHEMISTRY, 1999, 38 (20) :6386-6396