Ultracentrifugation versus kit exosome isolation: nanoLC–MS and other tools reveal similar performance biomarkers, but also contaminations

Author:

Skottvoll Frøydis Sved1,Berg Henriette Engen1,Bjørseth Kamilla1,Lund Kaja2,Roos Norbert3,Bekhradnia Sara1,Thiede Bernd3,Sandberg Cecilie4,Vik-Mo Einar Osland45,Roberg-Larsen Hanne1,Nyström Bo1,Lundanes Elsa1,Wilson Steven Ray1

Affiliation:

1. Department of Chemistry, University of Oslo, Post Box 1033, Blindern, NO-0315 Oslo, Norway

2. Department of Microbiology, Unit Cell Signaling, Oslo University Hospital, Gaustadalleen 34, NO-0372 Oslo, Norway

3. Department of Biosciences, University of Oslo, Post Box 1066, Blindern, NO-0316 Oslo, Norway

4. Institute for Surgical Research & Department of Neurosurgery, Vilhelm Magnus Laboratory of Neurosurgical Research, Oslo University Hospital, 4950 Nydalen, NO-0424 Oslo, Norway

5. Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Post Box 1171, Blindern, 0318 Oslo, Norway

Abstract

Aim: For isolation of exosomes, differential ultracentrifugation and an isolation kit from a major vendor were compared. Materials & methods: ‘Case study’ exosomes isolated from patient-derived cells from glioblastoma multiforme and a breast cancer cell line were analyzed. Results: Transmission electron microscopy, dynamic light scattering, western blotting, and so forth, revealed comparable performance. Potential protein biomarkers for both diseases were also identified in the isolates using nanoLC–MS. Western blotting and nanoLC–MS also revealed negative exosome markers regarding both isolation approaches. Conclusion: The two isolation methods had an overall similar performance, but we hesitate to use the term ‘exosome isolation’ as impurities may be present with both isolation methods. NanoLC–MS can detect disease biomarkers in exosomes and is useful for critical assessment of exosome enrichment procedures.

Publisher

Future Science Ltd

Subject

Biotechnology

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