Kofoed Eric M, Vance Russell E
Division of Immunology and Pathogenesis, Department of Molecular and Cell Biology, University of California, Berkeley, CA, USA.
Methods Mol Biol. 2013;1040:169-83. doi: 10.1007/978-1-62703-523-1_13.
Inflammasomes are large cytosolic multi-protein complexes that form in response to infection and other stimuli, and play an important role in the innate immune response. Traditional methods for assaying inflammasome activation have relied on detection of autoproteolysis of the cysteine protease caspase-1, or proteolytic processing of its substrate, the inflammatory cytokine IL-1β. These measurements report on the final output of inflammasome activation, but do not assess inflammasome assembly and composition. Here we describe the application of blue native gel electrophoresis as a tool for investigating stimulus-dependent inflammasome assembly and for identification of individual components within the multi-protein complex.
炎性小体是大型胞质多蛋白复合物,在受到感染和其他刺激时形成,并在先天免疫反应中发挥重要作用。传统的炎性小体激活检测方法依赖于检测半胱氨酸蛋白酶caspase-1的自蛋白水解,或其底物炎性细胞因子IL-1β的蛋白水解加工。这些测量报告了炎性小体激活的最终结果,但没有评估炎性小体的组装和组成。在这里,我们描述了蓝色原胶电泳作为一种工具的应用,用于研究刺激依赖性炎性小体组装以及鉴定多蛋白复合物中的单个成分。