A high-throughput system for two-hybrid screening based on growth curve analysis in microtiter plates

被引:18
作者
Diaz-Camino, C [1 ]
Risseeuw, EP [1 ]
Liu, E [1 ]
Crosby, WL [1 ]
机构
[1] Natl Res Council Canada, Inst Plant Biotechnol, Gene Express Grp, Saskatoon, SK S7N 0W9, Canada
基金
美国国家科学基金会;
关键词
two-hybrid screening; two-hybrid quantification; protein protein interactions; yeast; Saccharomyces cerevisiae;
D O I
10.1016/S0003-2697(02)00706-6
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The yeast two-hybrid system is a powerful tool for identifying novel protein-protein interactions. In general, biochemical marker genes such as lacZ are exploited for indirect quantification of the interaction, and commonly involve the conduct of rather laborious beta-galactosidase assays. This paper describes a simple alternative method based on growth curve analysis of yeast cultures that is amenable to microtiter plate format, and therefore allows the quantification of large numbers of yeast two-hybrid combinations. The analyzed results of yeast cultures grown in microtiter plates were compared with those obtained from the classical beta-galactosidase assay. We conclude that the method presented here is reproducible, of equal or greater sensitivity than the beta-galactosidase assay, and can be further adapted for application to the conduct of large-scale, automated yeast two-hybrid experiments. (C) 2003 Published by Elsevier Science (USA).
引用
收藏
页码:171 / 174
页数:4
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