Kerppola Tom K
Cold Spring Harb Protoc. 2013 Aug 1;2013(8):727-31. doi: 10.1101/pdb.prot076497.
Bimolecular fluorescence complementation (BiFC) analysis enables direct visualization of protein interactions and modifications in living cells. It is based on the facilitated association of two nonfluorescent fragments of a fluorescent protein fused to putative interaction partners. The intrinsic fluorescence of the active complex enables detection of protein interactions with high sensitivity, fine spatial resolution, and minimal perturbation of the cells. This protocol outlines methods to analyze protein interactions in cultured mammalian cells using BiFC, but can be readily adapted to any cell type or aerobically grown organism that can be genetically modified to express the fusion proteins.
双分子荧光互补(BiFC)分析能够直接观察活细胞中的蛋白质相互作用和修饰。它基于与假定相互作用伙伴融合的荧光蛋白的两个无荧光片段的易化结合。活性复合物的固有荧光能够以高灵敏度、良好的空间分辨率以及对细胞的最小扰动来检测蛋白质相互作用。本方案概述了使用BiFC分析培养的哺乳动物细胞中蛋白质相互作用的方法,但可以很容易地适用于任何能够进行基因改造以表达融合蛋白的细胞类型或需氧生长的生物体。