Sui Hongyan, Chen Qian, Imamichi Tomozumi
Laboratory of Human Retrovirology and Immunoinformatics, Frederick National Laboratory for Cancer Research, Bldg. 550, Rm 126,1050 Boyles Street, Frederick, MD 21702 United States.
MethodsX. 2020 Apr 13;7:100890. doi: 10.1016/j.mex.2020.100890. eCollection 2020.
Innate immune response is insisted upon detection of foreign intracellular DNA or RNA derived from viruses and bacteria. This reaction is important to initiate an effective protective response for the host cells. This crucial step is induced by cytosolic nucleic acids sensors/binding proteins, which triggers the production of type I or type III interferons (IFNs) and proinflammatory cytokines such as Interleukin 6 (IL-6). The identification of these cytosolic DNA or RNA sensors is a key step in understanding the signaling pathways triggered by those pathogens. Here we describe an effective approach to identify potential known/novel DNA or RNA sensors: a pull-down assay using DNA/RNA-conjugated beads with a customized competition strategy, which conferred a more effective and efficient way to determine the interaction between DNA/RNA and the sensor protein(s), therefore greatly improves the progress to investigate potential novel cytosolic DNA or RNA sensors/ binding proteins •The customized method makes the traditional pull-down assays more effective and efficient to identify DNA/RNA binding protein(s).•With the competitor of your choice, the method provides specific information about the competitive binding between DNA/RNA and binding proteins.
天然免疫反应依赖于对源自病毒和细菌的胞内异源DNA或RNA的检测。这种反应对于启动宿主细胞的有效保护反应很重要。这一关键步骤由胞质核酸传感器/结合蛋白诱导,其触发I型或III型干扰素(IFN)以及促炎细胞因子如白细胞介素6(IL-6)的产生。识别这些胞质DNA或RNA传感器是理解由这些病原体触发的信号通路的关键一步。在此,我们描述一种识别潜在已知/新型DNA或RNA传感器的有效方法:使用DNA/RNA偶联磁珠并采用定制竞争策略的下拉实验,该策略提供了一种更有效且高效的方式来确定DNA/RNA与传感器蛋白之间的相互作用,从而极大地推进了对潜在新型胞质DNA或RNA传感器/结合蛋白的研究进程。•定制方法使传统下拉实验在识别DNA/RNA结合蛋白方面更有效且高效。•借助您选择的竞争者,该方法可提供有关DNA/RNA与结合蛋白之间竞争性结合的具体信息。