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Polymeric hydrophilic ionic liquids used to modify magnetic nanoparticles for the highly selective enrichment of N-linked glycopeptides
The low abundance of glycopeptides in biological samples makes it necessary to enrich them before further analysis. In this study, the polymeric hydrophilic ionic liquid-modified magnetic (Fe(3)O(4)@MPS@PMAC) nanoparticles were synthesized via a one-step reflux-precipitation polymerization. Owing to...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5539331/ https://www.ncbi.nlm.nih.gov/pubmed/28765562 http://dx.doi.org/10.1038/s41598-017-07516-x |
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author | Jiao, Fenglong Gao, Fangyuan Wang, Heping Deng, Yulin Zhang, Yangjun Qian, Xiaohong Zhang, Yukui |
author_facet | Jiao, Fenglong Gao, Fangyuan Wang, Heping Deng, Yulin Zhang, Yangjun Qian, Xiaohong Zhang, Yukui |
author_sort | Jiao, Fenglong |
collection | PubMed |
description | The low abundance of glycopeptides in biological samples makes it necessary to enrich them before further analysis. In this study, the polymeric hydrophilic ionic liquid-modified magnetic (Fe(3)O(4)@MPS@PMAC) nanoparticles were synthesized via a one-step reflux-precipitation polymerization. Owing to the excellent hydrophilicity and strong electrostatic interaction toward glycopeptides of the polymerized hydrophilic ionic liquid, [2-(methacryloyloxy) ethyl] trimethylammonium chloride (MAC), the synthesized Fe(3)O(4)@MPS@PMAC nanoparticles exhibited outstanding performance in glycopeptide enrichment with high detection sensitivity (10 fmol), large binding capacity (100 μg mg(−1)) and satisfied enrichment recovery (approximately 82%). Furthermore, the newly developed Fe(3)O(4)@MPS@PMAC nanoparticles were applied for the glycopeptide enrichment of HeLa exosome proteins. A total of 1274 glycopeptides from 536 glycoproteins were identified in three replicate analyses of 50 μg of HeLa exosome proteins. These results demonstrate the potential of Fe(3)O(4)@MPS@PMAC nanoparticles for both glycoproteomic analysis and exosome research. |
format | Online Article Text |
id | pubmed-5539331 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55393312017-08-07 Polymeric hydrophilic ionic liquids used to modify magnetic nanoparticles for the highly selective enrichment of N-linked glycopeptides Jiao, Fenglong Gao, Fangyuan Wang, Heping Deng, Yulin Zhang, Yangjun Qian, Xiaohong Zhang, Yukui Sci Rep Article The low abundance of glycopeptides in biological samples makes it necessary to enrich them before further analysis. In this study, the polymeric hydrophilic ionic liquid-modified magnetic (Fe(3)O(4)@MPS@PMAC) nanoparticles were synthesized via a one-step reflux-precipitation polymerization. Owing to the excellent hydrophilicity and strong electrostatic interaction toward glycopeptides of the polymerized hydrophilic ionic liquid, [2-(methacryloyloxy) ethyl] trimethylammonium chloride (MAC), the synthesized Fe(3)O(4)@MPS@PMAC nanoparticles exhibited outstanding performance in glycopeptide enrichment with high detection sensitivity (10 fmol), large binding capacity (100 μg mg(−1)) and satisfied enrichment recovery (approximately 82%). Furthermore, the newly developed Fe(3)O(4)@MPS@PMAC nanoparticles were applied for the glycopeptide enrichment of HeLa exosome proteins. A total of 1274 glycopeptides from 536 glycoproteins were identified in three replicate analyses of 50 μg of HeLa exosome proteins. These results demonstrate the potential of Fe(3)O(4)@MPS@PMAC nanoparticles for both glycoproteomic analysis and exosome research. Nature Publishing Group UK 2017-08-01 /pmc/articles/PMC5539331/ /pubmed/28765562 http://dx.doi.org/10.1038/s41598-017-07516-x Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Jiao, Fenglong Gao, Fangyuan Wang, Heping Deng, Yulin Zhang, Yangjun Qian, Xiaohong Zhang, Yukui Polymeric hydrophilic ionic liquids used to modify magnetic nanoparticles for the highly selective enrichment of N-linked glycopeptides |
title | Polymeric hydrophilic ionic liquids used to modify magnetic nanoparticles for the highly selective enrichment of N-linked glycopeptides |
title_full | Polymeric hydrophilic ionic liquids used to modify magnetic nanoparticles for the highly selective enrichment of N-linked glycopeptides |
title_fullStr | Polymeric hydrophilic ionic liquids used to modify magnetic nanoparticles for the highly selective enrichment of N-linked glycopeptides |
title_full_unstemmed | Polymeric hydrophilic ionic liquids used to modify magnetic nanoparticles for the highly selective enrichment of N-linked glycopeptides |
title_short | Polymeric hydrophilic ionic liquids used to modify magnetic nanoparticles for the highly selective enrichment of N-linked glycopeptides |
title_sort | polymeric hydrophilic ionic liquids used to modify magnetic nanoparticles for the highly selective enrichment of n-linked glycopeptides |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5539331/ https://www.ncbi.nlm.nih.gov/pubmed/28765562 http://dx.doi.org/10.1038/s41598-017-07516-x |
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