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Ready-made chromatography columns for extracellular vesicle isolation from plasma

Proteomic studies of circulating vesicles are hampered by difficulties in purifying vesicles from plasma and serum. Isolations are contaminated with high-abundance blood proteins that may mask genuine vesicular-associated proteins and/or simply provide misleading data. In this brief report, we explo...

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Autores principales: Welton, Joanne Louise, Webber, Jason Paul, Botos, Laur-Alexandru, Jones, Michael, Clayton, Aled
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Co-Action Publishing 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4376847/
https://www.ncbi.nlm.nih.gov/pubmed/25819214
http://dx.doi.org/10.3402/jev.v4.27269
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author Welton, Joanne Louise
Webber, Jason Paul
Botos, Laur-Alexandru
Jones, Michael
Clayton, Aled
author_facet Welton, Joanne Louise
Webber, Jason Paul
Botos, Laur-Alexandru
Jones, Michael
Clayton, Aled
author_sort Welton, Joanne Louise
collection PubMed
description Proteomic studies of circulating vesicles are hampered by difficulties in purifying vesicles from plasma and serum. Isolations are contaminated with high-abundance blood proteins that may mask genuine vesicular-associated proteins and/or simply provide misleading data. In this brief report, we explored the potential utility of a commercially available size exclusion chromatography column for rapid vesicle purification. We evaluated the performance of the column, with cancer cell line conditioned medium or healthy donor plasma, in terms of removing non-vesicular protein and enriching for vesicles exhibiting exosome characteristics. Serial fractions revealed a peak for typical exosomal proteins (CD9, CD81 etc.) that preceded the peak for highly abundant proteins, including albumin, for either sample type, and harvesting only this peak would represent elimination of >95% of protein from the sample. The columns showed good reproducibility, and streamlining the workflow would allow the exosome-relevant material to be collected in less than 10 minutes. Surprisingly, however, subsequent post-column vesicle concentration steps whilst resulting in some protein loss also lead to low vesicle recoveries, with a net effect of reducing sample purity (assessed by the particle-to-protein ratio). The columns provide a convenient, reproducible and highly effective means of eliminating >95% of non-vesicular protein from biological fluid samples such as plasma.
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spelling pubmed-43768472015-04-02 Ready-made chromatography columns for extracellular vesicle isolation from plasma Welton, Joanne Louise Webber, Jason Paul Botos, Laur-Alexandru Jones, Michael Clayton, Aled J Extracell Vesicles Short Report Proteomic studies of circulating vesicles are hampered by difficulties in purifying vesicles from plasma and serum. Isolations are contaminated with high-abundance blood proteins that may mask genuine vesicular-associated proteins and/or simply provide misleading data. In this brief report, we explored the potential utility of a commercially available size exclusion chromatography column for rapid vesicle purification. We evaluated the performance of the column, with cancer cell line conditioned medium or healthy donor plasma, in terms of removing non-vesicular protein and enriching for vesicles exhibiting exosome characteristics. Serial fractions revealed a peak for typical exosomal proteins (CD9, CD81 etc.) that preceded the peak for highly abundant proteins, including albumin, for either sample type, and harvesting only this peak would represent elimination of >95% of protein from the sample. The columns showed good reproducibility, and streamlining the workflow would allow the exosome-relevant material to be collected in less than 10 minutes. Surprisingly, however, subsequent post-column vesicle concentration steps whilst resulting in some protein loss also lead to low vesicle recoveries, with a net effect of reducing sample purity (assessed by the particle-to-protein ratio). The columns provide a convenient, reproducible and highly effective means of eliminating >95% of non-vesicular protein from biological fluid samples such as plasma. Co-Action Publishing 2015-03-26 /pmc/articles/PMC4376847/ /pubmed/25819214 http://dx.doi.org/10.3402/jev.v4.27269 Text en © 2015 Joanne Louise Welton et al. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Report
Welton, Joanne Louise
Webber, Jason Paul
Botos, Laur-Alexandru
Jones, Michael
Clayton, Aled
Ready-made chromatography columns for extracellular vesicle isolation from plasma
title Ready-made chromatography columns for extracellular vesicle isolation from plasma
title_full Ready-made chromatography columns for extracellular vesicle isolation from plasma
title_fullStr Ready-made chromatography columns for extracellular vesicle isolation from plasma
title_full_unstemmed Ready-made chromatography columns for extracellular vesicle isolation from plasma
title_short Ready-made chromatography columns for extracellular vesicle isolation from plasma
title_sort ready-made chromatography columns for extracellular vesicle isolation from plasma
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4376847/
https://www.ncbi.nlm.nih.gov/pubmed/25819214
http://dx.doi.org/10.3402/jev.v4.27269
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