Confounding factors of ultrafiltration and protein analysis in extracellular vesicle research

Abstract Identification and validation of extracellular vesicle (EV)-associated biomarkers requires robust isolation and characterization protocols. We assessed the impact of some commonly implemented pre-analytical, analytical and post-analytical variables in EV research. Centrifugal filters with d...

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Autores principales: Glenn Vergauwen, Bert Dhondt, Jan Van Deun, Eva De Smedt, Geert Berx, Evy Timmerman, Kris Gevaert, Ilkka Miinalainen, Véronique Cocquyt, Geert Braems, Rudy Van den Broecke, Hannelore Denys, Olivier De Wever, An Hendrix
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Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/73e31ea4b0ec498d9cc6ac7a74bf4799
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spelling oai:doaj.org-article:73e31ea4b0ec498d9cc6ac7a74bf47992021-12-02T11:40:21ZConfounding factors of ultrafiltration and protein analysis in extracellular vesicle research10.1038/s41598-017-02599-y2045-2322https://doaj.org/article/73e31ea4b0ec498d9cc6ac7a74bf47992017-06-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-02599-yhttps://doaj.org/toc/2045-2322Abstract Identification and validation of extracellular vesicle (EV)-associated biomarkers requires robust isolation and characterization protocols. We assessed the impact of some commonly implemented pre-analytical, analytical and post-analytical variables in EV research. Centrifugal filters with different membrane types and pore sizes are used to reduce large volume biofluids prior to EV isolation or to concentrate EVs. We compared five commonly reported filters for their efficiency when using plasma, urine and EV-spiked PBS. Regenerated cellulose membranes with pore size of 10 kDa recovered EVs the most efficient. Less than 40% recovery was achieved with other filters. Next, we analyzed the effect of the type of protein assays to measure EV protein in colorimetric and fluorometric kits. The fluorometric assay Qubit measured low concentration EV and BSA samples the most accurately with the lowest variation among technical and biological replicates. Lastly, we quantified Optiprep remnants in EV samples from density gradient ultracentrifugation and demonstrate that size-exclusion chromatography efficiently removes Optiprep from EVs. In conclusion, choice of centrifugal filters and protein assays confound EV analysis and should be carefully considered to increase efficiency towards biomarker discovery. SEC-based removal of Optiprep remnants from EVs can be considered for downstream applications.Glenn VergauwenBert DhondtJan Van DeunEva De SmedtGeert BerxEvy TimmermanKris GevaertIlkka MiinalainenVéronique CocquytGeert BraemsRudy Van den BroeckeHannelore DenysOlivier De WeverAn HendrixNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-12 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Glenn Vergauwen
Bert Dhondt
Jan Van Deun
Eva De Smedt
Geert Berx
Evy Timmerman
Kris Gevaert
Ilkka Miinalainen
Véronique Cocquyt
Geert Braems
Rudy Van den Broecke
Hannelore Denys
Olivier De Wever
An Hendrix
Confounding factors of ultrafiltration and protein analysis in extracellular vesicle research
description Abstract Identification and validation of extracellular vesicle (EV)-associated biomarkers requires robust isolation and characterization protocols. We assessed the impact of some commonly implemented pre-analytical, analytical and post-analytical variables in EV research. Centrifugal filters with different membrane types and pore sizes are used to reduce large volume biofluids prior to EV isolation or to concentrate EVs. We compared five commonly reported filters for their efficiency when using plasma, urine and EV-spiked PBS. Regenerated cellulose membranes with pore size of 10 kDa recovered EVs the most efficient. Less than 40% recovery was achieved with other filters. Next, we analyzed the effect of the type of protein assays to measure EV protein in colorimetric and fluorometric kits. The fluorometric assay Qubit measured low concentration EV and BSA samples the most accurately with the lowest variation among technical and biological replicates. Lastly, we quantified Optiprep remnants in EV samples from density gradient ultracentrifugation and demonstrate that size-exclusion chromatography efficiently removes Optiprep from EVs. In conclusion, choice of centrifugal filters and protein assays confound EV analysis and should be carefully considered to increase efficiency towards biomarker discovery. SEC-based removal of Optiprep remnants from EVs can be considered for downstream applications.
format article
author Glenn Vergauwen
Bert Dhondt
Jan Van Deun
Eva De Smedt
Geert Berx
Evy Timmerman
Kris Gevaert
Ilkka Miinalainen
Véronique Cocquyt
Geert Braems
Rudy Van den Broecke
Hannelore Denys
Olivier De Wever
An Hendrix
author_facet Glenn Vergauwen
Bert Dhondt
Jan Van Deun
Eva De Smedt
Geert Berx
Evy Timmerman
Kris Gevaert
Ilkka Miinalainen
Véronique Cocquyt
Geert Braems
Rudy Van den Broecke
Hannelore Denys
Olivier De Wever
An Hendrix
author_sort Glenn Vergauwen
title Confounding factors of ultrafiltration and protein analysis in extracellular vesicle research
title_short Confounding factors of ultrafiltration and protein analysis in extracellular vesicle research
title_full Confounding factors of ultrafiltration and protein analysis in extracellular vesicle research
title_fullStr Confounding factors of ultrafiltration and protein analysis in extracellular vesicle research
title_full_unstemmed Confounding factors of ultrafiltration and protein analysis in extracellular vesicle research
title_sort confounding factors of ultrafiltration and protein analysis in extracellular vesicle research
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/73e31ea4b0ec498d9cc6ac7a74bf4799
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