Hampshire Andrew J, Rusling David A, Broughton-Head Victoria J, Fox Keith R
School of Biological Sciences, University of Southampton, Bassett Crescent East, Southampton SO16 7PX, UK.
Methods. 2007 Jun;42(2):128-40. doi: 10.1016/j.ymeth.2007.01.002.
Footprinting is a simple method for assessing the sequence selectivity of DNA-binding ligands. The method is based on the ability of the ligand to protect DNA from cleavage at its binding site. This review describes the use of DNase I and hydroxyl radicals, the most commonly used footprinting probes, in footprinting experiments. The success of a footprinting experiment depends on using an appropriate DNA substrate and we describe how these can best be chosen or designed. Although footprinting was originally developed for assessing a ligand's sequence selectivity, it can also be employed to estimate the binding strength (quantitative footprinting) and to assess the association and dissociation rate constants for slow binding reactions.
足迹法是一种评估DNA结合配体序列选择性的简单方法。该方法基于配体保护DNA在其结合位点不被切割的能力。本综述描述了在足迹实验中最常用的足迹探针——DNase I和羟基自由基的使用。足迹实验的成功取决于使用合适的DNA底物,我们将描述如何最好地选择或设计这些底物。尽管足迹法最初是为评估配体的序列选择性而开发的,但它也可用于估计结合强度(定量足迹法)以及评估慢结合反应的缔合和解离速率常数。