Department of Biochemical Engineering and Biotechnology, Indian Institute of Technology, New Delhi, India.
PLoS One. 2018 Aug 23;13(8):e0202602. doi: 10.1371/journal.pone.0202602. eCollection 2018.
Transcription of a gene can be regulated at many different levels. One such fundamental level is interaction between protein and DNA. Protein(s) binds to distinct sites on the DNA, which activate, enhance or repress transcription. Despite being such an important process, very few tools exist to identify the proteins that interact with chromosome, most of which are in vitro in nature. Here, we propose an in vivo based method for identification of DNA binding protein(s) in bacteria where the DNA-protein complex formed in vivo is crosslinked by formaldehyde. This complex is further isolated and the bound proteins are identified. The method was used to isolate promoter DNA binding proteins, which bind and regulate the dsz operon in Gordonia sp. IITR 100 responsible for biodesulfurization of organosulfurs. The promoter binding proteins were identified by MALDI ToF MS/MS and the binding was confirmed by gel shift assay. Unlike other reported in vivo methods, this improved method does not require sequence of the whole genome or a chip and can be scaled up to improve yields.
基因转录可以在多个不同水平上进行调控。其中一个基本的调控水平是蛋白质与 DNA 的相互作用。蛋白质(s)结合到 DNA 上的特定位点,这些位点可以激活、增强或抑制转录。尽管这是一个非常重要的过程,但目前很少有工具可以识别与染色体相互作用的蛋白质,其中大多数都是体外的。在这里,我们提出了一种基于体内的方法,用于鉴定细菌中的 DNA 结合蛋白,其中在体内形成的 DNA-蛋白质复合物通过甲醛交联。进一步分离这个复合物,并鉴定结合的蛋白质。该方法用于分离启动子 DNA 结合蛋白,这些蛋白结合并调节 Gordonia sp. IITR 100 中的 dsz 操纵子,该操纵子负责有机硫的生物脱硫。通过 MALDI ToF MS/MS 鉴定启动子结合蛋白,并通过凝胶迁移实验证实了结合。与其他报道的体内方法不同,这种改进的方法不需要整个基因组的序列或芯片,并且可以扩展以提高产量。