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Fluorescence Recovery Assay for the Detection of Protein-DNA Binding

机译:荧光恢复测定法检测蛋白质-DNA结合

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We report a novel and straightforward fluorescence recovery assay which enables the detection of protein-DNA interactions and simultaneously determines relative binding affinities of sequence-specific DNA-binding proteins for a variety of DNA sequences in a multiplexed format. The detection of protein-DNA binding is accomplished by monitoring fluorescence recovery during exonuclease digestion of DNA sequences that are modified with fluorophore-quencher pairs. Retardation of fluorescence recovery occurs with binding of the protein to the putative DNA binding element, which arrests exonuclease digestion. The assay detects protein-DNA binding in a homogeneous solution simply, quickly, and reliably without using radioisotopes. Multiplexing is possible by labeling different DNA sequences with spectrally distinct dyes, allowing simultaneous analysis of experimental and control binding reactions in the same mixture.
机译:我们报告了一种新颖而直接的荧光回收检测方法,该检测方法能够检测蛋白质-DNA相互作用,并同时确定多种DNA序列的多重形式的序列特异性DNA结合蛋白的相对结合亲和力。蛋白质-DNA结合的检测是通过监测核酸外切酶消化被荧光团-猝灭剂对修饰的DNA序列的荧光恢复来完成的。蛋白质与假定的DNA结合元件的结合会导致荧光恢复的延迟,这会阻止核酸外切酶的消化。该方法无需使用放射性同位素即可简单,快速且可靠地检测均质溶液中的蛋白质-DNA结合。通过用光谱不同的染料标记不同的DNA序列,可以实现多重分析,从而可以同时分析同一混合物中的实验和对照结合反应。

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