双分子荧光互补
荧光
生物
荧光蛋白
多蛋白复合物
蛋白质-蛋白质相互作用
绿色荧光蛋白
互补
费斯特共振能量转移
黄色荧光蛋白
蛋白质片段互补分析
生物物理学
细胞生物学
植物细胞
生物化学
基因
物理
表型
量子力学
作者
Dan Weinthal,Tzvi Tzfira
标识
DOI:10.1016/j.tplants.2008.11.002
摘要
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.
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