Département Médicaments et Technologies pour la Santé (DMTS), Université Paris-Saclay, CEA, INRAE, SPI, Bagnols-sur-Cèze, France.
Methods Mol Biol. 2022;2452:167-182. doi: 10.1007/978-1-0716-2111-0_11.
A comprehensive cartography of viral and host proteins expressed during the different stages of SARS-CoV-2 infection is key to decipher the molecular mechanisms of pathogenesis. For the most detailed analysis, proteins should be first purified and then proteolyzed with trypsin in the presence of detergents. The resulting peptide mixtures are resolved by reverse phase ultrahigh pressure liquid chromatography and then identified by a high-resolution tandem mass spectrometer. The thousands of spectra acquired for each fraction can then be assigned to peptide sequences using a relevant protein sequence database, comprising viral and host proteins and potential contaminants from the growth medium or from the operator. The peptides are evidencing proteins and their intensities are used to infer the abundance of their corresponding proteins. Data analysis allows for highlighting the viral and host proteins dynamics. Here, we describe the sample preparation method adapted to profile SARS-CoV-2 -infected cell models, the shotgun proteomics pipeline to record experimental data, and the workflow for data interpretation to analyze infection-induced proteomic changes in a time-resolved manner.
对 SARS-CoV-2 感染不同阶段表达的病毒和宿主蛋白进行全面的图谱绘制,是解码发病机制分子机制的关键。为了进行最详细的分析,应首先将蛋白质纯化,然后在去污剂存在的情况下用胰蛋白酶进行蛋白水解。所得肽混合物通过反相超高压液相色谱法进行分离,然后用高分辨率串联质谱仪进行鉴定。然后,使用包含病毒和宿主蛋白以及来自生长培养基或操作人员的潜在污染物的相关蛋白质序列数据库,将每个馏分获得的数千个光谱分配给肽序列。肽是证明蛋白质存在的证据,其强度可用于推断其相应蛋白质的丰度。数据分析可突出病毒和宿主蛋白的动态变化。在这里,我们描述了适应分析 SARS-CoV-2 感染细胞模型的样品制备方法、记录实验数据的鸟枪法蛋白质组学管道,以及用于以时间分辨方式分析感染诱导的蛋白质组变化的工作流程。