Kerppola Tom K
Cold Spring Harb Protoc. 2013 Aug 1;2013(8):714-8. doi: 10.1101/pdb.top076489.
Bimolecular fluorescence complementation (BiFC) analysis enables direct visualization of protein interactions 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. As discussed in more detail here, BiFC analysis requires careful consideration of the design and expression of the fusion proteins for the results to be interpretable.
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。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促进结合。活性复合物的固有荧光能够以高灵敏度、良好的空间分辨率和对细胞的最小扰动检测蛋白质相互作用。如本文更详细讨论的,BiFC分析需要仔细考虑融合蛋白的设计和表达,以便结果能够被解释。