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双分子荧光互补(BiFC)分析作为活细胞中蛋白质相互作用的一种检测方法。

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

作者信息

Kerppola Tom K

机构信息

Howard Hughes Medical Institute and Department of Biological Chemistry, University of Michigan Medical School, Ann Arbor, Michigan 48109-0650, USA.

出版信息

Annu Rev Biophys. 2008;37:465-87. doi: 10.1146/annurev.biophys.37.032807.125842.

Abstract

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.

摘要

蛋白质相互作用是产生生物调节特异性的基本机制。对活细胞中蛋白质相互作用的研究具有特殊意义,因为特定细胞中发生的相互作用取决于细胞中存在的全部蛋白质以及影响该细胞的外部刺激。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。BiFC检测基于荧光蛋白的两个非荧光片段之间的关联,当它们通过与片段融合的蛋白质之间的相互作用彼此靠近时。使用BiFC检测已经在许多不同的细胞类型和生物体中观察到了大量的蛋白质相互作用。BiFC检测在技术上很简单,可以使用标准的分子生物学和细胞培养试剂以及常规的荧光显微镜或流式细胞仪进行。

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