4.5 Article

Exosome enrichment of human serum using multiple cycles of centrifugation

Journal

ELECTROPHORESIS
Volume 36, Issue 17, Pages 2017-2026

Publisher

WILEY
DOI: 10.1002/elps.201500131

Keywords

Centrifugation; Exosomes; Human serum; Mass spectrometry; Ultracentrifugation

Funding

  1. National Institutes of Health [R01GM49500]
  2. National Cancer Institute [R21CA189775]
  3. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education, Science and Technology [2010-0010776]
  4. National Research Foundation of Korea [2010-0010776] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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In this work, we compared the use of repeated cycles of centrifugation at conventional speeds for enrichment of exosomes from human serum compared to the use of ultracentrifugation (UC). After removal of cells and cell debris, a speed of 110000 x g or 40000 x g was used for the UC or centrifugation enrichment process, respectively. The enriched exosomes were analyzed using the bicinchoninic acid assay, 1D gel separation, transmission electron microscopy, Western blotting, and high-resolution LC-MS/MS analysis. It was found that a five-cycle repetition of UC or centrifugation is necessary for successful removal of nonexosomal proteins in the enrichment of exosomes from human serum. More significantly, 5x centrifugation enrichment was found to provide similar or better performance than 5x UC enrichment in terms of enriched exosome protein amount, Western blot band intensity for detection of CD-63, and numbers of identified exosome-related proteins and cluster of differentiation (CD) proteins. A total of 478 proteins were identified in the LC-MS/MS analyses of exosome proteins obtained from 5x UCs and 5x centrifugations including many important CD membrane proteins. The presence of previously reported exosome-related proteins including key exosome protein markers demonstrates the utility of this method for analysis of proteins in human serum.

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