Department of Immunology, Genetics & Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
JSPS Overseas Research Fellow, Japan Society for the Promotion of Science, Tokyo, Japan.
Commun Biol. 2022 Dec 22;5(1):1402. doi: 10.1038/s42003-022-04349-x.
Extracellular vesicles (EVs) are mediators of intercellular communication and a promising class of biomarkers. Surface proteins of EVs play decisive roles in establishing a connection with recipient cells, and they are putative targets for diagnostic assays. Analysis of the surface proteins can thus both illuminate the biological functions of EVs and help identify potential biomarkers. We developed a strategy combining high-resolution mass spectrometry (HRMS) and proximity ligation assays (PLA) to first identify and then validate surface proteins discovered on EVs. We applied our workflow to investigate surface proteins of small EVs found in seminal fluid (SF-sEV). We identified 1,014 surface proteins and verified the presence of a subset of these on the surface of SF-sEVs. Our work demonstrates a general strategy for deep analysis of EVs' surface proteins across patients and pathological conditions, proceeding from unbiased screening by HRMS to ultra-sensitive targeted analyses via PLA.
细胞外囊泡(EVs)是细胞间通讯的介质,也是一类很有前途的生物标志物。EVs 的表面蛋白在与受体细胞建立连接方面起着决定性作用,它们是诊断检测的潜在靶点。因此,分析表面蛋白既能阐明 EVs 的生物学功能,又有助于鉴定潜在的生物标志物。我们开发了一种结合高分辨率质谱(HRMS)和邻近连接分析(PLA)的策略,首先鉴定然后验证 EV 表面发现的蛋白。我们将我们的工作流程应用于研究精液(SF-sEV)中小 EV 表面的蛋白。我们鉴定了 1014 种表面蛋白,并验证了其中一部分存在于 SF-sEV 的表面。我们的工作展示了一种针对患者和病理状况下 EV 表面蛋白进行深入分析的通用策略,从 HRMS 的无偏筛选到通过 PLA 进行超灵敏靶向分析。