荧光各向异性
核酸
化学
荧光
表位
肽
寡核苷酸
蛋白质-蛋白质相互作用
配体结合分析
小分子
生物化学
生物物理学
生物
抗原
DNA
受体
遗传学
量子力学
物理
膜
标识
DOI:10.1002/9780470559277.ch090102
摘要
Abstract The technique of fluorescence polarization (FP) is based on the observation that when a fluorescently labeled molecule is excited by polarized light, it emits light with a degree of polarization that is inversely proportional to the rate of molecular rotation. This property of fluorescence can be used to measure the interaction of a small labeled ligand with a larger protein and provides a basis for direct and competition binding assays. FP assays are readily adaptable to a high‐throughput format, have been used successfully in screens directed against a wide range of targets, and are particularly valuable in screening for inhibitors of protein‐protein and protein‐nucleic acid interactions when a small binding epitope can be identified for one of the partners. The protocols in this article describe a general procedure for development of FP assays to monitor binding of such a peptide or oligonucleotide to a protein of interest. Curr. Protoc. Chem Biol . 1:1‐15. © 2009 by John Wiley & Sons, Inc.
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