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Recovery, overloading, and protein interactions in asymmetrical flow field-flow fractionation
In asymmetrical flow field-flow fractionation (AF4), similar to other separation techniques, mass recovery and overloading require special attention in order to obtain quantitative results. We conducted a systematic study with five globular proteins of different molecular weight (36.7–669 kDa) and i...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6459789/ https://www.ncbi.nlm.nih.gov/pubmed/30790023 http://dx.doi.org/10.1007/s00216-019-01673-w |
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author | Marioli, Maria Kok, Wim Th. |
author_facet | Marioli, Maria Kok, Wim Th. |
author_sort | Marioli, Maria |
collection | PubMed |
description | In asymmetrical flow field-flow fractionation (AF4), similar to other separation techniques, mass recovery and overloading require special attention in order to obtain quantitative results. We conducted a systematic study with five globular proteins of different molecular weight (36.7–669 kDa) and isoelectric point (4.0–6.5), and ultrafiltration membranes that are commonly used in aqueous AF4, regenerated cellulose (RC) and polyethersulfone (PES). Phosphate-buffered saline (PBS) with ionic strength 0.15 M and pH 7.2 was used as the carrier liquid in this study. The actual molecular weight cutoff (MWCO) was found to be higher than the nominal value and varied between membranes of different chemistry but the same nominal MWCO. Adsorption on the membrane was found to be dependent on the membrane chemistry (RC had lower adsorption compared to PES), and independent of the protein standard for the examined proteins. On the other hand, the mass overloading effects (i.e., higher retention times, peak broadening, and fronting peaks) were significantly more pronounced for γ-globulin than for the other proteins. The overloading effects could be rationalized with the increase of the local viscosity close to the membrane, depending on the properties of the proteins, and we derived theoretical equations that related the dependency of the migration velocity on the protein concentration through this non-ideal viscosity effect. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00216-019-01673-w) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6459789 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-64597892019-05-03 Recovery, overloading, and protein interactions in asymmetrical flow field-flow fractionation Marioli, Maria Kok, Wim Th. Anal Bioanal Chem Research Paper In asymmetrical flow field-flow fractionation (AF4), similar to other separation techniques, mass recovery and overloading require special attention in order to obtain quantitative results. We conducted a systematic study with five globular proteins of different molecular weight (36.7–669 kDa) and isoelectric point (4.0–6.5), and ultrafiltration membranes that are commonly used in aqueous AF4, regenerated cellulose (RC) and polyethersulfone (PES). Phosphate-buffered saline (PBS) with ionic strength 0.15 M and pH 7.2 was used as the carrier liquid in this study. The actual molecular weight cutoff (MWCO) was found to be higher than the nominal value and varied between membranes of different chemistry but the same nominal MWCO. Adsorption on the membrane was found to be dependent on the membrane chemistry (RC had lower adsorption compared to PES), and independent of the protein standard for the examined proteins. On the other hand, the mass overloading effects (i.e., higher retention times, peak broadening, and fronting peaks) were significantly more pronounced for γ-globulin than for the other proteins. The overloading effects could be rationalized with the increase of the local viscosity close to the membrane, depending on the properties of the proteins, and we derived theoretical equations that related the dependency of the migration velocity on the protein concentration through this non-ideal viscosity effect. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00216-019-01673-w) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2019-02-21 2019 /pmc/articles/PMC6459789/ /pubmed/30790023 http://dx.doi.org/10.1007/s00216-019-01673-w Text en © The Author(s) 2019 OpenAccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Research Paper Marioli, Maria Kok, Wim Th. Recovery, overloading, and protein interactions in asymmetrical flow field-flow fractionation |
title | Recovery, overloading, and protein interactions in asymmetrical flow field-flow fractionation |
title_full | Recovery, overloading, and protein interactions in asymmetrical flow field-flow fractionation |
title_fullStr | Recovery, overloading, and protein interactions in asymmetrical flow field-flow fractionation |
title_full_unstemmed | Recovery, overloading, and protein interactions in asymmetrical flow field-flow fractionation |
title_short | Recovery, overloading, and protein interactions in asymmetrical flow field-flow fractionation |
title_sort | recovery, overloading, and protein interactions in asymmetrical flow field-flow fractionation |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6459789/ https://www.ncbi.nlm.nih.gov/pubmed/30790023 http://dx.doi.org/10.1007/s00216-019-01673-w |
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