Fielding Lauren A, Deweese Joseph
Department of Biological, Physical, and Human Sciences, Freed-Hardeman University, Henderson, TN, USA.
Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN, USA.
Methods Mol Biol. 2025;2928:115-122. doi: 10.1007/978-1-0716-4550-5_11.
The topoisomerase II N-terminal ATPase clamp stabilization assay can determine the relative stability of the topoisomerase-DNA interaction. After allowing the protein and purified DNA to interact for a fixed amount of time, the protein:DNA complexes are then bound to a glass fiber filter where a series of washes of increasing stringency are applied. These washes can disrupt the protein:DNA interaction depending on the strength of the complex and whether the N-terminal domain, referred to here as the "clamp," has closed around the DNA. The DNA flow through from each step can be concentrated and then quantified using gel electrophoresis. This approach enables researchers to examine what conditions tend to stabilize the enzyme:DNA complexes.
拓扑异构酶II N端ATP酶钳夹稳定分析可确定拓扑异构酶与DNA相互作用的相对稳定性。使蛋白质与纯化的DNA相互作用一段固定时间后,将蛋白质:DNA复合物结合到玻璃纤维滤膜上,在此进行一系列严格程度递增的洗涤。这些洗涤可根据复合物的强度以及N端结构域(此处称为“钳夹”)是否已围绕DNA闭合来破坏蛋白质:DNA相互作用。每一步的DNA流出物可进行浓缩,然后使用凝胶电泳进行定量。这种方法使研究人员能够研究哪些条件倾向于稳定酶:DNA复合物。