Clarke Paul, Cuív Páraic O, O'Connell Michael
School of Biotechnology, Dublin City University Glasnevin, Dublin 9, Ireland.
Nucleic Acids Res. 2005 Feb 1;33(2):e18. doi: 10.1093/nar/gni011.
Since its initial description, the yeast two-hybrid (Y2H) system has been widely used for the detection and analysis of protein-protein interactions. Mating-based strategies have been developed permitting its application for automated proteomic interaction mapping projects using both exhaustive and high-throughput strategies. More recently, a number of prokaryotic two-hybrid (P2H) systems have been developed but, despite the many advantages such Escherichia coli-based systems have over the Y2H system, they have not yet been widely implemented for proteomic interaction mapping. This may be largely due to the fact that high-throughput strategies employing bacterial transformation are not as amenable to automation as Y2H mating-based strategies. Here, we describe the construction of novel conjugative P2H system vectors. These vectors carry a mobilization element of the IncPalpha group plasmid RP4 and can therefore be mobilized with high efficiency from an E.coli donor strain encoding all of the required transport functions in trans. We demonstrate how these vectors permit the exploitation of bacterial conjugation for technically simplified and automated proteomic interaction mapping strategies in E.coli, analogous to the mating-based strategies developed for the Y2H system.
自首次被描述以来,酵母双杂交(Y2H)系统已被广泛用于蛋白质-蛋白质相互作用的检测和分析。基于交配的策略已得到发展,使其能够应用于使用穷举法和高通量策略的自动化蛋白质组相互作用图谱绘制项目。最近,已经开发了许多原核双杂交(P2H)系统,但是,尽管基于大肠杆菌的系统相对于Y2H系统有许多优点,但它们尚未广泛应用于蛋白质组相互作用图谱绘制。这可能主要是因为采用细菌转化的高通量策略不如基于Y2H交配的策略那样易于自动化。在这里,我们描述了新型接合P2H系统载体的构建。这些载体携带IncPα组质粒RP4的转移元件,因此可以从反式编码所有所需转运功能的大肠杆菌供体菌株中高效转移。我们展示了这些载体如何利用细菌接合在大肠杆菌中实现技术上简化和自动化的蛋白质组相互作用图谱绘制策略,这类似于为Y2H系统开发的基于交配的策略。