Park Sang-Hyun, Raines Ronald T
Department of Cellular and Molecular Pharmacology, University of California-San Francisco, San Francisco, CA, USA.
Methods Mol Biol. 2004;261:161-6. doi: 10.1385/1-59259-762-9:161.
A fluorescence polarization assay can be used to evaluate the strength of a protein-protein interaction. A green fluorescent protein variant is fused to one of the protein partners. The formation of a complex is then deduced from an increase in fluorescence polarization, and the equilibrium dissociation constant of the complex is determined in a homogeneous aqueous environment. The assay is demonstrated by using the interaction of the S-protein and S-peptide fragments of ribonuclease A as a case study.
荧光偏振测定法可用于评估蛋白质-蛋白质相互作用的强度。将绿色荧光蛋白变体与其中一个蛋白质伴侣融合。然后根据荧光偏振的增加推断复合物的形成,并在均匀的水性环境中测定复合物的平衡解离常数。以核糖核酸酶A的S蛋白和S肽片段的相互作用为例对该测定法进行了说明。