Chambers Jacob R, Sauer Karin
Department of Biological Sciences, Binghamton Biofilm Research Center, Binghamton University, 2219 Biotechnology Building, 85 Murray Hill Rd., Binghamton, NY, 13902, USA.
Department of Biological Sciences, Binghamton Biofilm Research Center (BBRC), Binghamton University, 2401 ITC Building, 85 Murray Hill Road, Binghamton, NY, 13902, USA.
Methods Mol Biol. 2017;1657:293-302. doi: 10.1007/978-1-4939-7240-1_23.
Modulation of signal transduction via binding of the secondary messenger molecule cyclic di-GMP to effector proteins is a near universal regulatory schema in bacteria. In particular, direct binding of c-di-GMP to transcriptional regulators has been shown to alter gene expression of a variety of processes. Here, we illustrate a pull-down-based DNA:protein binding reaction to determine the relative importance of c-di-GMP in the binding affinity of a target protein to specific DNA sequences. Specifically, the pull-down-based assay enables DNA binding to be analyzed with differing concentrations of c-di-GMP in the absence/presence of specific and nonspecific competitors.
通过第二信使分子环二鸟苷酸(c-di-GMP)与效应蛋白结合来调节信号转导,是细菌中一种几乎普遍存在的调控模式。特别是,已表明c-di-GMP与转录调节因子的直接结合会改变多种过程的基因表达。在此,我们展示了一种基于下拉实验的DNA:蛋白质结合反应,以确定c-di-GMP在靶蛋白与特定DNA序列结合亲和力中的相对重要性。具体而言,基于下拉实验的分析方法能够在存在/不存在特异性和非特异性竞争者的情况下,用不同浓度的c-di-GMP来分析DNA结合情况。