Lee Andrea J, Warshaw David M, Wallace Susan S
Department of Microbiology and Molecular Genetics, The Markey Center for Molecular Genetics, The University of Vermont, 95 Carrigan Drive, Stafford Hall, Burlington, VT 05405-0084, USA.
Department of Molecular Physiology and Biophysics, The University of Vermont, Health Science Research Facility, 149 Beaumont Avenue, Burlington, VT 05405-0075, USA.
DNA Repair (Amst). 2014 Aug;20:23-31. doi: 10.1016/j.dnarep.2014.01.007. Epub 2014 Feb 20.
The first step of base excision repair utilizes glycosylase enzymes to find damage within a genome. A persistent question in the field of DNA repair is how glycosylases interact with DNA to specifically find and excise target damaged bases with high efficiency and specificity. Ensemble studies have indicated that glycosylase enzymes rely upon both sliding and distributive modes of search, but ensemble methods are limited in their ability to directly observe these modes. Here we review insights into glycosylase scanning behavior gathered through single-molecule fluorescence studies of enzyme interactions with DNA and provide a context for these results in relation to ensemble experiments.
碱基切除修复的第一步利用糖基化酶在基因组中寻找损伤。DNA修复领域一个长期存在的问题是糖基化酶如何与DNA相互作用,以高效且特异的方式特异性地找到并切除目标损伤碱基。整体研究表明,糖基化酶依靠滑动和分布搜索模式,但整体方法在直接观察这些模式的能力上存在局限。在此,我们回顾通过酶与DNA相互作用的单分子荧光研究获得的关于糖基化酶扫描行为的见解,并结合整体实验为这些结果提供背景。