| Literature DB >> 18622019 |
Kourosh Zolghadr1, Oliver Mortusewicz, Ulrich Rothbauer, Regina Kleinhans, Heike Goehler, Erich E Wanker, M Cristina Cardoso, Heinrich Leonhardt.
Abstract
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.Mesh:
Substances:
Year: 2008 PMID: 18622019 DOI: 10.1074/mcp.M700548-MCP200
Source DB: PubMed Journal: Mol Cell Proteomics ISSN: 1535-9476 Impact factor: 5.911