Zolghadr Kourosh, Mortusewicz Oliver, Rothbauer Ulrich, Kleinhans Regina, Goehler Heike, Wanker Erich E, Cardoso M Cristina, Leonhardt Heinrich
Munich Center for Integrated Protein Science (CiPSM) and Department of Biology, Ludwig Maximilians University Munich, 82152 Planegg-Martinsried, Germany.
Mol Cell Proteomics. 2008 Nov;7(11):2279-87. doi: 10.1074/mcp.M700548-MCP200. Epub 2008 Jul 12.
Genetic high throughput screens have yielded large sets of potential protein-protein interactions now to be verified and further investigated. Here we present a simple assay to directly visualize protein-protein interactions in single living cells. Using a modified lac repressor system, we tethered a fluorescent bait at a chromosomal lac operator array and assayed for co-localization of fluorescent prey fusion proteins. With this fluorescent two-hybrid assay we successfully investigated the interaction of proteins from different subcellular compartments including nucleus, cytoplasm, and mitochondria. In combination with an S phase marker we also studied the cell cycle dependence of protein-protein interactions. These results indicate that the fluorescent two-hybrid assay is a powerful tool to investigate protein-protein interactions within their cellular environment and to monitor the response to external stimuli in real time.
基因高通量筛选已经产生了大量有待验证和进一步研究的潜在蛋白质-蛋白质相互作用。在此,我们展示了一种简单的检测方法,可直接在单个活细胞中可视化蛋白质-蛋白质相互作用。利用改良的乳糖阻遏物系统,我们将一种荧光诱饵拴系在染色体乳糖操纵子阵列上,并检测荧光猎物融合蛋白的共定位情况。通过这种荧光双杂交检测法,我们成功研究了来自不同亚细胞区室(包括细胞核、细胞质和线粒体)的蛋白质之间的相互作用。结合S期标记物,我们还研究了蛋白质-蛋白质相互作用对细胞周期的依赖性。这些结果表明,荧光双杂交检测法是一种强大的工具,可用于在细胞环境中研究蛋白质-蛋白质相互作用,并实时监测对外部刺激的反应。