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Facile synthesis of hydrophilic magnetic graphene nanocomposites via dopamine self-polymerization and Michael addition for selective enrichment of N-linked glycopeptides

The development of methods to effectively capture N-glycopeptides from the complex biological samples is crucial to N-glycoproteome profiling. Herein, the hydrophilic chitosan–functionalized magnetic graphene nanocomposites (denoted as Fe(3)O(4)-GO@PDA-Chitosan) were designed and synthesized via a s...

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Autores principales: Bi, Changfen, Yuan, Ye, Tu, Yuran, Wu, Jiahui, Liang, Yulu, Li, Yiliang, He, Xiwen, Chen, Langxing, Zhang, Yukui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6952460/
https://www.ncbi.nlm.nih.gov/pubmed/31919391
http://dx.doi.org/10.1038/s41598-019-56944-4
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author Bi, Changfen
Yuan, Ye
Tu, Yuran
Wu, Jiahui
Liang, Yulu
Li, Yiliang
He, Xiwen
Chen, Langxing
Zhang, Yukui
author_facet Bi, Changfen
Yuan, Ye
Tu, Yuran
Wu, Jiahui
Liang, Yulu
Li, Yiliang
He, Xiwen
Chen, Langxing
Zhang, Yukui
author_sort Bi, Changfen
collection PubMed
description The development of methods to effectively capture N-glycopeptides from the complex biological samples is crucial to N-glycoproteome profiling. Herein, the hydrophilic chitosan–functionalized magnetic graphene nanocomposites (denoted as Fe(3)O(4)-GO@PDA-Chitosan) were designed and synthesized via a simple two-step modification (dopamine self-polymerization and Michael addition). The Fe(3)O(4)-GO@PDA-Chitosan nanocomposites exhibited good performances with low detection limit (0.4 fmol·μL(−1)), good selectivity (mixture of bovine serum albumin and horseradish peroxidase tryptic digests at a molar ration of 10:1), good repeatability (4 times), high binding capacity (75 mg·g(−1)). Moreover, Fe(3)O(4)-GO@PDA-Chitosan nanocomposites were further utilized to selectively enrich glycopeptides from human renal mesangial cell (HRMC, 200 μg) tryptic digest, and 393 N-linked glycopeptides, representing 195 different glycoproteins and 458 glycosylation sites were identified. This study provides a feasible strategy for the surface functionalized novel materials for isolation and enrichment of N-glycopeptides.
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spelling pubmed-69524602020-01-14 Facile synthesis of hydrophilic magnetic graphene nanocomposites via dopamine self-polymerization and Michael addition for selective enrichment of N-linked glycopeptides Bi, Changfen Yuan, Ye Tu, Yuran Wu, Jiahui Liang, Yulu Li, Yiliang He, Xiwen Chen, Langxing Zhang, Yukui Sci Rep Article The development of methods to effectively capture N-glycopeptides from the complex biological samples is crucial to N-glycoproteome profiling. Herein, the hydrophilic chitosan–functionalized magnetic graphene nanocomposites (denoted as Fe(3)O(4)-GO@PDA-Chitosan) were designed and synthesized via a simple two-step modification (dopamine self-polymerization and Michael addition). The Fe(3)O(4)-GO@PDA-Chitosan nanocomposites exhibited good performances with low detection limit (0.4 fmol·μL(−1)), good selectivity (mixture of bovine serum albumin and horseradish peroxidase tryptic digests at a molar ration of 10:1), good repeatability (4 times), high binding capacity (75 mg·g(−1)). Moreover, Fe(3)O(4)-GO@PDA-Chitosan nanocomposites were further utilized to selectively enrich glycopeptides from human renal mesangial cell (HRMC, 200 μg) tryptic digest, and 393 N-linked glycopeptides, representing 195 different glycoproteins and 458 glycosylation sites were identified. This study provides a feasible strategy for the surface functionalized novel materials for isolation and enrichment of N-glycopeptides. Nature Publishing Group UK 2020-01-09 /pmc/articles/PMC6952460/ /pubmed/31919391 http://dx.doi.org/10.1038/s41598-019-56944-4 Text en © The Author(s) 2020 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
Bi, Changfen
Yuan, Ye
Tu, Yuran
Wu, Jiahui
Liang, Yulu
Li, Yiliang
He, Xiwen
Chen, Langxing
Zhang, Yukui
Facile synthesis of hydrophilic magnetic graphene nanocomposites via dopamine self-polymerization and Michael addition for selective enrichment of N-linked glycopeptides
title Facile synthesis of hydrophilic magnetic graphene nanocomposites via dopamine self-polymerization and Michael addition for selective enrichment of N-linked glycopeptides
title_full Facile synthesis of hydrophilic magnetic graphene nanocomposites via dopamine self-polymerization and Michael addition for selective enrichment of N-linked glycopeptides
title_fullStr Facile synthesis of hydrophilic magnetic graphene nanocomposites via dopamine self-polymerization and Michael addition for selective enrichment of N-linked glycopeptides
title_full_unstemmed Facile synthesis of hydrophilic magnetic graphene nanocomposites via dopamine self-polymerization and Michael addition for selective enrichment of N-linked glycopeptides
title_short Facile synthesis of hydrophilic magnetic graphene nanocomposites via dopamine self-polymerization and Michael addition for selective enrichment of N-linked glycopeptides
title_sort facile synthesis of hydrophilic magnetic graphene nanocomposites via dopamine self-polymerization and michael addition for selective enrichment of n-linked glycopeptides
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6952460/
https://www.ncbi.nlm.nih.gov/pubmed/31919391
http://dx.doi.org/10.1038/s41598-019-56944-4
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