β galactosidase complementation:: A cell-based luminescent assay platform for drug discovery

被引:58
作者
Olson, Keith R. [1 ]
Eglen, Richard M. [1 ]
机构
[1] DicoveRx Corp, Fremont, CA USA
关键词
D O I
10.1089/adt.2006.052
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Many cell-based assays interrogating cell pathway activation employ protocols that require microscopic imaging techniques. However, such assays are not in general widely adopted for primary screening. Protein complementation, particularly of enzymes, provides an alternative approach for cell pathway analysis, with a principal advantage that is amenable to high throughput screening using microtiter plate protocols. Notably, alpha complementation of the enzyme beta-galactosidase has been exploited as a technology in this regard, using substrates that generates luminescent signals. This review describes the various uses of this flexible technology to cell-based assay development.
引用
收藏
页码:137 / 144
页数:8
相关论文
共 46 条
[1]   α-Complemented β-galactosidase.: An in vivo model substrate for the molecular chaperone heat-shock protein 90 in yeast [J].
Abbas-Terki, T ;
Picard, D .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1999, 266 (02) :517-523
[2]   Epidermal growth factor receptor dimerization monitored in live cells [J].
Blakely, BT ;
Rossi, FMV ;
Tillotson, B ;
Palmer, M ;
Estelles, A ;
Blau, HM .
NATURE BIOTECHNOLOGY, 2000, 18 (02) :218-222
[3]   Evaluation of the InteraX™ System technology in a high-throughput screening environment [J].
Büttner, FH ;
Kumpf, R ;
Menzel, S ;
Reulle, D ;
Valler, MJ .
JOURNAL OF BIOMOLECULAR SCREENING, 2005, 10 (05) :485-494
[4]  
COTY WA, 1994, J CLIN IMMUNOASSAY, V17, P144
[5]  
Cregger M, 2006, ARCH PATHOL LAB MED, V130, P1026
[6]   Enzyme fragment complementation: A flexible high throughput screening assay technology [J].
Eglen, RM .
ASSAY AND DRUG DEVELOPMENT TECHNOLOGIES, 2002, 1 (01) :97-104
[7]  
EGLEN RM, 2003, COMBIN CHEM HTS, V6, P313
[8]   A homogeneous cell-based assay to measure nuclear translocation using β-galactosidase enzyme fragment complementation [J].
Fung, P. ;
Peng, K. ;
Kobel, P. ;
Dotimas, H. ;
Kauffman, L. ;
Olson, K. ;
Eglen, R. M. .
ASSAY AND DRUG DEVELOPMENT TECHNOLOGIES, 2006, 4 (03) :263-272
[9]   Advances in high content screening for drug discovery [J].
Giuliano, KA ;
Haskins, JR ;
Taylor, DL .
ASSAY AND DRUG DEVELOPMENT TECHNOLOGIES, 2003, 1 (04) :565-577
[10]   A homogeneous enzyme fragment complementation cyclic AMP screen for GPCR agonists [J].
Golla, R ;
Seethala, R .
JOURNAL OF BIOMOLECULAR SCREENING, 2002, 7 (06) :515-525