Hammer Elke, Darm Katrin, Völker Uwe
Abteilung für Funktionelle Genomforschung, Interfakultäres Institut für Genetik und Funktionelle Genomforschung, Universitätsmedizin Greifswald, Greifswald, Germany.
Methods Mol Biol. 2013;1005:67-76. doi: 10.1007/978-1-62703-386-2_6.
Proteomic profiling of heart tissue might help to discover the molecular events related to or even causing cardiovascular diseases in human. However, this material is rare and only available from biopsies taken for diagnostics, e.g., assessment of inflammatory events or virus persistence. Within this chapter, we describe a workflow for the quantitative proteome analysis of heart biopsies. Starting with 1-2 mg of tissue material, crude protein extracts were prepared, digested with LysC and trypsin, and then analyzed by LC-ESI-tandem mass spectrometry. Due to the low technical variance, the method can be used for label-free quantitation of disease-specific alterations in the human heart. Methods discussed include homogenization of biopsy tissue, sample preparation, proteolytic digestion, as well as data analysis for label-free quantitation.
心脏组织的蛋白质组分析可能有助于发现与人类心血管疾病相关甚至导致心血管疾病的分子事件。然而,这种材料很罕见,仅可从用于诊断的活检样本中获得,例如评估炎症事件或病毒持续性。在本章中,我们描述了一种用于心脏活检定量蛋白质组分析的工作流程。从1-2毫克组织材料开始,制备粗蛋白提取物,用LysC和胰蛋白酶消化,然后通过液相色谱-电喷雾串联质谱进行分析。由于技术差异小,该方法可用于对人类心脏中疾病特异性改变进行无标记定量。讨论的方法包括活检组织的匀浆、样品制备、蛋白水解消化以及无标记定量的数据分析。