New technologies for high-throughput screening

被引:101
作者
Burbaum, JJ [1 ]
Sigal, NH [1 ]
机构
[1] Pharmacopeia Inc, Princeton, NJ 08540 USA
关键词
D O I
10.1016/S1367-5931(97)80111-1
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
To screen efficiently the millions of compounds that are synthesized using combinatorial and automated methods, dramatically improved assay technologies are currently needed. In 96-well microtiter plates, nonradioactive techniques (primarily fluorimetric) and cell-based functional methods have moved to the cutting edge, while clever assays that extract information from large bead-based combinatorial libraries have begun to show considerable promise. In the future, miniaturized assays that break out of the 96-well format will be enabled by innovative technologies for high-throughput screening.
引用
收藏
页码:72 / 78
页数:7
相关论文
共 40 条
[1]   Simultaneous quantitation of diphtheria and tetanus antibodies by double antigen, time-resolved fluorescence immunoassay [J].
Aggerbeck, H ;
NorgaardPedersen, B ;
Heron, I .
JOURNAL OF IMMUNOLOGICAL METHODS, 1996, 190 (02) :171-183
[2]  
Akong M., 1995, Society for Neuroscience Abstracts, V21, P577
[3]  
BRAN MR, 1996, J BIOMOL SCREEN, V1, P43
[4]  
BRAYNEROSBORNE H, 1995, EUR J PHARMACOL, V296, P93
[5]  
Broach JR, 1996, NATURE, V384, P14
[6]  
BRONSTEIN I, 1990, BIOTECHNIQUES, V8, P310
[7]  
Bronstein I, 1996, CLIN CHEM, V42, P1542
[8]  
Cantor C., 1980, BIOPHYSICAL CHEM, P451
[9]   A NEW NONISOTOPIC DETECTION SYSTEM FOR IMMUNOASSAYS [J].
DEAVER, DR .
NATURE, 1995, 377 (6551) :758-760
[10]   Enzyme-triggered formation of electrochemiluminescent ruthenium complexes [J].
Dong, LW ;
Martin, MT .
ANALYTICAL BIOCHEMISTRY, 1996, 236 (02) :344-347