Choi Dong-Sic, Gho Yong Song
Department of Life Sciences, Pohang University of Science and Technology, 77 Cheongam-Ro, Nam-Gu, Pohang, Gyeongbuk, 790-784, Republic of Korea.
Methods Mol Biol. 2015;1295:167-77. doi: 10.1007/978-1-4939-2550-6_14.
Extracellular vesicles are nano-sized lipid bilayer vesicles released from most cells, including archaea, bacteria, and eukaryotic cells. These membrane vesicles play multiple roles in cell-to-cell communication, including immune modulation, angiogenesis, and transformation of cells by transferring genetic material and functional proteins. They contain specific subsets of proteins, DNA, RNA, and lipids that represent their cellular status. Furthermore, extracellular vesicles are enriched in cell type- or disease-specific vesicular proteins, especially plasma membrane proteins, which have pathophysiological functions; these vesicular proteins are considered novel diagnostic biomarkers as well as therapeutic targets. To profile the proteome, various purification methods of extracellular vesicles have been developed, but density gradient ultracentrifugation is considered the most promising. In this chapter, we describe the isolation of extracellular vesicles derived from SW480 cells and the preparation of tryptic peptides for mass-spectrometry-based proteomic analysis.
细胞外囊泡是从大多数细胞释放的纳米级脂质双层囊泡,这些细胞包括古细菌、细菌和真核细胞。这些膜囊泡在细胞间通讯中发挥多种作用,包括免疫调节、血管生成以及通过转移遗传物质和功能蛋白实现细胞转化。它们包含代表其细胞状态的特定蛋白质、DNA、RNA和脂质亚群。此外,细胞外囊泡富含具有病理生理功能的细胞类型或疾病特异性囊泡蛋白,尤其是质膜蛋白;这些囊泡蛋白被认为是新型诊断生物标志物以及治疗靶点。为了分析蛋白质组,已经开发了多种细胞外囊泡的纯化方法,但密度梯度超速离心被认为是最有前景的方法。在本章中,我们描述了从SW480细胞中分离细胞外囊泡以及制备用于基于质谱的蛋白质组分析的胰蛋白酶肽段的方法。