Biomolecular fluorescence complementation (BiFC) analysis as a probe of protein interactions in living cells

被引:482
作者
Kerppola, Tom K. [1 ,2 ]
机构
[1] Univ Michigan, Sch Med, Howard Hughes Med Inst, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Dept Biol Chem, Ann Arbor, MI 48109 USA
关键词
fluorescence imaging; subcellular localization; visualization of molecular complexes; multicolor BiFC analysis;
D O I
10.1146/annurev.biophys.37.032807.125842
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Protein interactions are a fundamental mechanism for the generation of biological regulatory specificity. The study of protein interactions in living cells is of particular significance because the interactions that occur in a particular cell depend on the full complement of proteins present in the cell and the external stimuli that influence the cell. Bimolecular fluorescence complementation (BiFC),analysis enables direct visualization of protein interactions in living cells. The BiFC assay is based on the association between two nonfluorescent fragments of a fluorescent protein when they are brought in proximity to each other by an interaction between proteins fused to the fragments. Numerous protein interactions have been visualized using the BiFC assay in many different cell types and organisms. The BiFC assay is technically straightforward and can be performed using standard molecular biology and cell culture reagents and a regular fluorescence microscope or flow cytometer.
引用
收藏
页码:465 / 487
页数:23
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