Ozyhar A, Kiltz H H
Lehrstuhl für Biochemie, Fakultät Chemie, Ruhr Universität Bochum, Germany.
J Chromatogr. 1991 Nov 29;587(1):11-7. doi: 10.1016/0021-9673(91)85192-i.
The mobility shift assay is a well established method for proving binding of protein to DNA. However, this method depends on the stability of the protein-DNA complex during the electrophoretic process. Ecdysteroid receptor shows a strong tendency to aggregate under low-salt conditions of electrophoresis to a non DNA-binding form. We have developed a high-resolution gel filtration method which allows the interaction of ecdysteroid receptor with specific DNA sequences to be studied. The method seems to be generally applicable. It does not depend on the availability of a purified protein. Crude preparations could be used to characterize the stoichiometry and the molecular parameters of the complexes formed between DNA and DNA-binding proteins.
迁移率变动分析是一种用于证明蛋白质与DNA结合的成熟方法。然而,该方法依赖于蛋白质-DNA复合物在电泳过程中的稳定性。蜕皮甾类受体在低盐电泳条件下有强烈的聚集倾向,形成非DNA结合形式。我们开发了一种高分辨率凝胶过滤方法,可用于研究蜕皮甾类受体与特定DNA序列的相互作用。该方法似乎具有普遍适用性。它不依赖于纯化蛋白质的可得性。粗制制剂可用于表征DNA与DNA结合蛋白之间形成的复合物的化学计量和分子参数。