Weinthal Dan, Tzfira Tzvi
Department of Molecular, Cellular and Developmental Biology, University of Michigan, Ann Arbor, MI 48109-1048, USA.
Trends Plant Sci. 2009 Feb;14(2):59-63. doi: 10.1016/j.tplants.2008.11.002. Epub 2009 Jan 15.
The bimolecular fluorescence complementation (BiFC) assay is based on the reconstruction of a fluorescent signal upon the interaction of two protein partners fused to two non-fluorescent fragments of an otherwise fluorescent protein. Interacting partners are typically tagged to fragments of the yellow fluorescent protein, but the use of other fluorescent proteins has been reported. By combining fragments of different types of fluorescent proteins, it is possible not only to detect pairwise protein-protein interaction but also to study the formation of multiprotein complexes in living cells. As we discuss here, a multicolor BiFC set of vectors has been recently deployed for visualizing the simultaneous formation of alternative protein kinase and calcium sensor complexes in living plant cells. This proof-of-concept report and the vectors that have been developed are an important addition to the sets of tools that are useful for analysing multiprotein complexes in plant cells.
双分子荧光互补(BiFC)分析基于以下原理:当两个与荧光蛋白的两个非荧光片段融合的蛋白质伴侣相互作用时,会重建荧光信号。相互作用的伴侣通常被标记为黄色荧光蛋白的片段,但也有使用其他荧光蛋白的报道。通过组合不同类型荧光蛋白的片段,不仅可以检测成对的蛋白质-蛋白质相互作用,还可以研究活细胞中多蛋白复合物的形成。正如我们在此讨论的,最近已部署了一组多色BiFC载体,用于可视化活植物细胞中替代蛋白激酶和钙传感器复合物的同时形成。这一概念验证报告以及所开发的载体是对用于分析植物细胞中多蛋白复合物的工具集的重要补充。