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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Co-Action Publishing
2015
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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. |
format | Online Article Text |
id | pubmed-4376847 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Co-Action Publishing |
record_format | MEDLINE/PubMed |
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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