Lihon Michelle V, Tuchscherer Nathan A, Tao W Andy
Department of Biochemistry, Purdue University, West Lafayette, IN, USA.
Department of Chemistry, Purdue University, West Lafayette, IN, USA.
Methods Mol Biol. 2025;2884:225-239. doi: 10.1007/978-1-0716-4298-6_15.
Extracellular vesicles (EVs) are small membrane-bound structures that play important roles in intercellular communication and the transfer of biomolecules between cells. EVs have become a topic of interest for research in translational proteomics for disease biomarker discovery due to their ability to reflect changes in the cellular proteome, including diseases affecting the brain. Utilizing the proteome analysis of EVs to its fullest potential requires proper isolation and purity. In this chapter, we describe a detailed method for the isolation and identification of brain tissue EVs for translational proteomics using our in-house chemical affinity magnetic bead-based (non-antibody) method, the EVtrap. We also discuss various methods for quantification, characterization, and functional analysis of isolated brain tissue EVs, including western blotting, and proteomic profiling of post-translational modifications (PTMs) involved in neurodegenerative diseases, such as protein N-terminal acetylation. This protocol provides a valuable resource for studies conducted on brain tissue EVs and their potential as biomarkers and therapeutic targets for neurological diseases.
细胞外囊泡(EVs)是小的膜结合结构,在细胞间通讯以及细胞间生物分子的传递中发挥重要作用。由于EVs能够反映细胞蛋白质组的变化,包括影响大脑的疾病,因此它们已成为转化蛋白质组学中用于疾病生物标志物发现研究的一个热门话题。要充分发挥EVs蛋白质组分析的潜力,需要进行适当的分离并保证纯度。在本章中,我们描述了一种详细的方法,即使用我们内部基于化学亲和磁珠(非抗体)的方法EVtrap,用于分离和鉴定用于转化蛋白质组学的脑组织EVs。我们还讨论了对分离出的脑组织EVs进行定量、表征和功能分析的各种方法,包括蛋白质免疫印迹,以及对神经退行性疾病中涉及的翻译后修饰(PTMs)进行蛋白质组分析,如蛋白质N端乙酰化。该方案为关于脑组织EVs及其作为神经疾病生物标志物和治疗靶点潜力的研究提供了宝贵资源。