Olorunniji Femi J, Rosser Susan J, Marshall Stark W
Institute of Molecular, Cell and Systems Biology, University of Glasgow, Bower Building, Glasgow, G12 8QQ, Scotland.
SynthSys-Synthetic and Systems Biology, School of Biological Sciences, University of Edinburgh, CH Waddington Building, The King's Buildings, Mayfield Road, Edinburgh, EH9 3JD, Scotland.
Methods Mol Biol. 2017;1642:229-245. doi: 10.1007/978-1-4939-7169-5_15.
Zinc finger recombinases (ZFRs) are designer site-specific recombinases that have been adapted for a variety of genome editing purposes. Due to their modular nature, ZFRs can be customized for targeted sequence recognition and recombination. There has been substantial research on the in vivo properties and applications of ZFRs; however, in order to fully understand and customize them, it will be necessary to study their properties in vitro. Experiments in vitro can allow us to optimize catalytic activities, improve target specificity, measure and minimize off-target activity, and characterize key steps in the recombination pathway that might be modified to improve performance. Here, we present a straightforward set of protocols for the expression and purification of ZFRs, an assay system for catalytic proficiency in vitro and bandshift assays for detection of sequence-specific DNA interactions.
锌指重组酶(ZFRs)是一种经过设计的位点特异性重组酶,已被应用于多种基因组编辑目的。由于其模块化性质,ZFRs可针对靶向序列识别和重组进行定制。目前已经对ZFRs的体内特性和应用进行了大量研究;然而,为了全面了解并对其进行定制,有必要在体外研究它们的特性。体外实验可以使我们优化催化活性、提高靶标特异性、测量并最小化脱靶活性,以及表征重组途径中可能被修饰以改善性能的关键步骤。在此,我们提供了一套简单的方案,用于ZFRs的表达和纯化、体外催化能力的检测系统以及用于检测序列特异性DNA相互作用的凝胶迁移实验。