Barnard Emma, McFerran Neil V, Trudgett Alan, Nelson John, Timson David J
School of Biological Sciences, Queen's University Belfast, Medical Biology Centre, 97 Lisburn Road, Belfast BT9 7BL, Northern Ireland, UK.
Biochem Soc Trans. 2008 Jun;36(Pt 3):479-82. doi: 10.1042/BST0360479.
BiFC (bimolecular fluorescence complementation) is a tool for investigating interactions between proteins. Non-fluorescent fragments of, for example, GFP (green fluorescent protein) are fused to the interacting partners. The interaction brings the fragments together, which then fold, reassemble and fluoresce. This process can be carried out in living cells and provides information both on the interaction and its subcellular location. We have developed a split-GFP-based BiFC assay for use in the budding yeast Saccharomyces cerevisiae in which the modifications are carried out at the genomic level, thus resulting in the tagged yeast proteins being expressed at wild-type levels. The system is capable of detecting interactions in all subcellular compartments tested (the cytoplasm, mitochondria and nucleus) and makes a valuable addition to techniques for the investigation of protein-protein interactions in this model organism.
双分子荧光互补(BiFC)是一种用于研究蛋白质之间相互作用的工具。例如,绿色荧光蛋白(GFP)的非荧光片段与相互作用的伙伴融合。相互作用使片段聚集在一起,然后折叠、重新组装并发出荧光。这个过程可以在活细胞中进行,并提供有关相互作用及其亚细胞定位的信息。我们开发了一种基于分裂型GFP的BiFC检测方法,用于酿酒酵母中,其中修饰是在基因组水平上进行的,从而使标记的酵母蛋白以野生型水平表达。该系统能够检测所有测试的亚细胞区室(细胞质、线粒体和细胞核)中的相互作用,为研究这种模式生物中蛋白质-蛋白质相互作用的技术增添了有价值的内容。