Möckli Natalie, Deplazes Anna, Hassa Paul O, Zhang Zhaolei, Peter Matthias, Hottiger Michael O, Stagljar Igor, Auerbach Daniel
Dualsystems Biotech AG, Zürich, Switzerland.
Biotechniques. 2007 Jun;42(6):725-30. doi: 10.2144/000112455.
Interactions between proteins are central to most biological processes; consequently, understanding the latter requires identification of all possible protein interactions within a cell. To extend the range of existing assays for the detection of protein interactions, we present a novel genetic screening assay, the cytosolic yeast two-hybrid system (cytoY2H), which is based on the split-ubiquitin technique and detects protein-protein interactions in the cytoplasm. We show that the assay can be applied to a wide range of proteins that are difficult to study in the classical yeast two-hybrid (Y2H) system, including transcription factors such as p53 and members of the NF-kappaB complex. Furthermore, we applied the cytoY2H system to cDNA library screening and identified several new interaction partners of Uri1p, an uncharacterized yeast protein. The cytoY2H system extends existing methods for the detection of protein interactions by providing a convenient solution for screening a wide range of transcriptionally active proteins.
蛋白质之间的相互作用是大多数生物过程的核心;因此,要理解这些生物过程,就需要识别细胞内所有可能的蛋白质相互作用。为了扩展现有蛋白质相互作用检测方法的范围,我们提出了一种新型遗传筛选方法——胞质酵母双杂交系统(cytoY2H),该系统基于分裂泛素技术,可检测细胞质中的蛋白质-蛋白质相互作用。我们证明,该方法可应用于多种在经典酵母双杂交(Y2H)系统中难以研究的蛋白质,包括转录因子如p53和NF-κB复合物成员。此外,我们将cytoY2H系统应用于cDNA文库筛选,并鉴定出未表征的酵母蛋白Uri1p的几个新的相互作用伙伴。cytoY2H系统通过为筛选多种转录活性蛋白提供便捷的解决方案,扩展了现有的蛋白质相互作用检测方法。