Division of Biomedical and Life Sciences, Faculty of Health and Medicine, Lancaster University, Lancaster, UK.
Methods Mol Biol. 2020;2116:125-137. doi: 10.1007/978-1-0716-0294-2_10.
Mass spectrometry based proteomics allows for the identification and quantification of protein and phosphorylation site abundance on a proteome wide scale. Here we describe the metabolic labeling of cultured Trypanosoma brucei cells in either the bloodstream or procyclic life cycle stage using stable isotope labeling of amino acids in cell culture (SILAC), and the production of samples suitable for analysis by liquid chromatography tandem mass spectrometry. The protocols require little specialist equipment, and they typically enable quantification of over 4500 proteins and 9000 phosphorylation sites.
基于质谱的蛋白质组学允许在蛋白质组范围内鉴定和定量蛋白质和磷酸化位点的丰度。在这里,我们描述了使用稳定同位素标记的细胞培养物中的氨基酸(SILAC)对培养的布氏锥虫细胞或前鞭毛体生活周期阶段进行代谢标记,并产生适合液相色谱串联质谱分析的样品。该方案需要很少的专业设备,通常可定量超过 4500 种蛋白质和 9000 个磷酸化位点。