Scientific Data (Nov 2023)

A proteomic meta-analysis refinement of plasma extracellular vesicles

  • Milene C. Vallejo,
  • Soumyadeep Sarkar,
  • Emily C. Elliott,
  • Hayden R. Henry,
  • Samantha M. Powell,
  • Ivo Diaz Ludovico,
  • Youngki You,
  • Fei Huang,
  • Samuel H. Payne,
  • Sasanka Ramanadham,
  • Emily K. Sims,
  • Thomas O. Metz,
  • Raghavendra G. Mirmira,
  • Ernesto S. Nakayasu

DOI
https://doi.org/10.1038/s41597-023-02748-1
Journal volume & issue
Vol. 10, no. 1
pp. 1 – 14

Abstract

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Abstract Extracellular vesicles play major roles in cell-to-cell communication and are excellent biomarker candidates. However, studying plasma extracellular vesicles is challenging due to contaminants. Here, we performed a proteomics meta-analysis of public data to refine the plasma EV composition by separating EV proteins and contaminants into different clusters. We obtained two clusters with a total of 1717 proteins that were depleted of known contaminants and enriched in EV markers with independently validated 71% true-positive. These clusters had 133 clusters of differentiation (CD) antigens and were enriched with proteins from cell-to-cell communication and signaling. We compared our data with the proteins deposited in PeptideAtlas, making our refined EV protein list a resource for mechanistic and biomarker studies. As a use case example for this resource, we validated the type 1 diabetes biomarker proplatelet basic protein in EVs and showed that it regulates apoptosis of β cells and macrophages, two key players in the disease development. Our approach provides a refinement of the EV composition and a resource for the scientific community.