Isolation and Identification of Brain Tissue Extracellular Vesicles for Translational Proteomics

Methods Mol Biol. 2025:2884:225-239. doi: 10.1007/978-1-0716-4298-6_15.

Abstract

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.

Keywords: Brain tissue; DDA; EVtrap; Exosomes; Extracellular vesicles (EVs); Label-free proteomics; Mass spectrometry; Relative quantitative proteomics; Tissue.

MeSH terms

  • Animals
  • Biomarkers / metabolism
  • Brain* / cytology
  • Brain* / metabolism
  • Extracellular Vesicles* / metabolism
  • Humans
  • Protein Processing, Post-Translational*
  • Proteome / metabolism
  • Proteomics* / methods

Substances

  • Proteome
  • Biomarkers