CURRENT TRENDS IN MOLECULAR RECOGNITION AND BIOSEPARATION

被引:52
作者
JONES, C
PATEL, A
GRIFFIN, S
MARTIN, J
YOUNG, P
ODONNELL, K
SILVERMAN, C
PORTER, T
CHAIKEN, I
机构
[1] SMITHKLINE BEECHAM PHARMACEUT,DEPT MOLEC IMMUNOL,KING OF PRUSSIA,PA 19406
[2] SMITHKLINE BEECHAM PHARMACEUT,DEPT PROT BIOCHEM,KING OF PRUSSIA,PA 19406
关键词
D O I
10.1016/0021-9673(95)00466-Z
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Molecular recognition guides the selective interaction of macromolecules with each other in essentially all biological processes. Perhaps the most impactful use of biomolecular recognition in separation science has been in affinity chromatography. The results of the last 26 years, since Cuatrecases, Wilchek and Anfinsen first reported the purification of staphylococcal nuclease, have validated the power of biomolecular specificity for purification. This power has stimulated an explosion of solid-phase ligand designs and affinity chromatographic applications. An ongoing case in point is the purification of recombinant proteins, which has been aided by engineering the proteins to contain Affinity-Tag sequences, such as hexa-histidine for metal-chelate separation and epitope sequence for separation by an immobilized monoclonal antibody. Tag technology can be adapted for plate assays and other solid-phase techniques. The advance of affinity chromatography also has stimulated immobilized ligand-based methods to characterize macromolecular recognition, including both chromatographic and optical biosensor methods. And, new methods such as phage display and other diversity library approaches continue to emerge to identify new recognition molecules of potential use as affinity ligands. Overall, it is tantalizing to envision a continued evolution of new affinity technologies which use the selectivity built into biomolecular recognition as a vehicle for purification, analysis, screening and other applications in separation sciences.
引用
收藏
页码:3 / 22
页数:20
相关论文
共 96 条
[41]   A RATIONAL APPROACH IN THE SEARCH FOR POTENT INHIBITORS AGAINST HIV PROTEINASE [J].
HUI, KY ;
MANETTA, JV ;
GYGI, T ;
BOWDON, BJ ;
KEITH, KA ;
SHANNON, WM ;
LAI, MHT .
FASEB JOURNAL, 1991, 5 (11) :2606-2610
[42]  
IIZUKA K, 1990, CHEM PHARM BULL, V38, P2487
[43]  
IMAI T, 1993, J BIOL CHEM, V268, P19681
[44]  
ISHI S, 1980, METHOD ENZYMOL, V80, P842
[45]  
JACKSON JR, 1995, J IMMUNOL, V154, P3310
[46]   GUIDING THE SELECTION OF HUMAN-ANTIBODIES FROM PHAGE DISPLAY REPERTOIRES TO A SINGLE EPITOPE OF AN ANTIGEN [J].
JESPERS, LS ;
ROBERTS, A ;
MAHLER, SM ;
WINTER, G ;
HOOGENBOOM, HR .
BIO-TECHNOLOGY, 1994, 12 (09) :899-903
[47]  
JOHANSON K, 1995, IN PRESS J BIOL CHEM
[48]   IMMOBILIZATION OF PROTEINS TO A CARBOXYMETHYLDEXTRAN-MODIFIED GOLD SURFACE FOR BIOSPECIFIC INTERACTION ANALYSIS IN SURFACE-PLASMON RESONANCE SENSORS [J].
JOHNSSON, B ;
LOFAS, S ;
LINDQUIST, G .
ANALYTICAL BIOCHEMISTRY, 1991, 198 (02) :268-277
[49]  
JONSSON U, 1991, BIOTECHNIQUES, V11, P620
[50]  
KASAI K, 1975, J BIOCHEM-TOKYO, V77, P261