Cho W, Hu Y, Baek K, Kim H
University of Illinois at Chicago, Chicago, IL, United States; Kyung Hee University, Yongin, South Korea.
University of Illinois at Chicago, Chicago, IL, United States.
Methods Enzymol. 2017;583:1-18. doi: 10.1016/bs.mie.2016.09.004. Epub 2016 Oct 21.
An increasing number of intracellular and extracellular proteins are shown to interact with membrane lipids under physiological conditions. For rapid and robust quantitative measurement of lipid-protein interaction, we developed a sensitive fluorescence quenching-based assay that is universally applicable to all proteins and lipids. The assay employs fluorescence protein (FP)-tagged proteins whose fluorescence emission intensity is decreased when they bind vesicles containing quenching lipids. This simple assay can be performed with a fluorescence plate reader or a spectrofluorometer and optimized for different proteins with various combinations of FPs and quenching lipids. The assay allows a rapid, sensitive, and accurate determination of lipid specificity and affinity for various lipid-binding proteins, and high-throughput screening of molecules that modulate their membrane binding.
越来越多的细胞内和细胞外蛋白质在生理条件下被证明能与膜脂相互作用。为了对脂-蛋白相互作用进行快速且可靠的定量测量,我们开发了一种基于荧光猝灭的灵敏检测方法,该方法普遍适用于所有蛋白质和脂质。该检测方法使用荧光蛋白(FP)标记的蛋白质,当它们与含有猝灭脂质的囊泡结合时,其荧光发射强度会降低。这种简单的检测可以用荧光酶标仪或荧光分光光度计进行,并针对不同的蛋白质,通过FP和猝灭脂质的各种组合进行优化。该检测方法能够快速、灵敏且准确地测定各种脂质结合蛋白的脂质特异性和亲和力,以及对调节其膜结合的分子进行高通量筛选。