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Maltose-Functionalized Hydrophilic Magnetic Nanoparticles with Polymer Brushes for Highly Selective Enrichment of N-Linked Glycopeptides

[Image: see text] Efficient enrichment glycoproteins/glycopeptides from complex biological solutions are very important in the biomedical sciences, in particular biomarker research. In this work, the high hydrophilic polyethylenimine conjugated polymaltose polymer brushes functionalized magnetic Fe(...

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Autores principales: Bi, Changfen, Liang, Yulu, Shen, Lijin, Tian, Shanshan, Zhang, Kai, Li, Yiliang, He, Xiwen, Chen, Langxing, Zhang, Yukui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044954/
https://www.ncbi.nlm.nih.gov/pubmed/30023808
http://dx.doi.org/10.1021/acsomega.7b01788
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author Bi, Changfen
Liang, Yulu
Shen, Lijin
Tian, Shanshan
Zhang, Kai
Li, Yiliang
He, Xiwen
Chen, Langxing
Zhang, Yukui
author_facet Bi, Changfen
Liang, Yulu
Shen, Lijin
Tian, Shanshan
Zhang, Kai
Li, Yiliang
He, Xiwen
Chen, Langxing
Zhang, Yukui
author_sort Bi, Changfen
collection PubMed
description [Image: see text] Efficient enrichment glycoproteins/glycopeptides from complex biological solutions are very important in the biomedical sciences, in particular biomarker research. In this work, the high hydrophilic polyethylenimine conjugated polymaltose polymer brushes functionalized magnetic Fe(3)O(4) nanoparticles (NPs) denoted as Fe(3)O(4)–PEI–pMaltose were designed and synthesized via a simple two-step modification. The obtained superhydrophilic Fe(3)O(4)–PEI–pMaltose NPs displayed outstanding advantages in the enrichment of N-linked glycopeptides, including high selectivity (1:100, mass ratios of HRP and bovine serum albumin (BSA) digest), low detection limit (10 fmol), large binding capacity (200 mg/g), and high enrichment recovery (above 85%). The above-mentioned excellent performance of novel Fe(3)O(4)–PEI–pMaltose NPs was attributed to graft of maltose polymer brushes and efficient assembly strategy. Moreover, Fe(3)O(4)–PEI–pMaltose NPs were further utilized to selectively enrich glycopeptides from human renal mesangial cell (HRMC, 200 μg) tryptic digest, and 449 N-linked glycopeptides, representing 323 different glycoproteins and 476 glycosylation sites, were identified. It was expected that the as-synthesized Fe(3)O(4)–PEI–pMaltose NPs, possessing excellent performance (high binding capacity, good selectivity, low detection limit, high enrichment recovery, and easy magnetic separation) coupled to a facile preparation procedure, have a huge potential in N-glycosylation proteome analysis of complex biological samples.
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spelling pubmed-60449542018-07-16 Maltose-Functionalized Hydrophilic Magnetic Nanoparticles with Polymer Brushes for Highly Selective Enrichment of N-Linked Glycopeptides Bi, Changfen Liang, Yulu Shen, Lijin Tian, Shanshan Zhang, Kai Li, Yiliang He, Xiwen Chen, Langxing Zhang, Yukui ACS Omega [Image: see text] Efficient enrichment glycoproteins/glycopeptides from complex biological solutions are very important in the biomedical sciences, in particular biomarker research. In this work, the high hydrophilic polyethylenimine conjugated polymaltose polymer brushes functionalized magnetic Fe(3)O(4) nanoparticles (NPs) denoted as Fe(3)O(4)–PEI–pMaltose were designed and synthesized via a simple two-step modification. The obtained superhydrophilic Fe(3)O(4)–PEI–pMaltose NPs displayed outstanding advantages in the enrichment of N-linked glycopeptides, including high selectivity (1:100, mass ratios of HRP and bovine serum albumin (BSA) digest), low detection limit (10 fmol), large binding capacity (200 mg/g), and high enrichment recovery (above 85%). The above-mentioned excellent performance of novel Fe(3)O(4)–PEI–pMaltose NPs was attributed to graft of maltose polymer brushes and efficient assembly strategy. Moreover, Fe(3)O(4)–PEI–pMaltose NPs were further utilized to selectively enrich glycopeptides from human renal mesangial cell (HRMC, 200 μg) tryptic digest, and 449 N-linked glycopeptides, representing 323 different glycoproteins and 476 glycosylation sites, were identified. It was expected that the as-synthesized Fe(3)O(4)–PEI–pMaltose NPs, possessing excellent performance (high binding capacity, good selectivity, low detection limit, high enrichment recovery, and easy magnetic separation) coupled to a facile preparation procedure, have a huge potential in N-glycosylation proteome analysis of complex biological samples. American Chemical Society 2018-02-07 /pmc/articles/PMC6044954/ /pubmed/30023808 http://dx.doi.org/10.1021/acsomega.7b01788 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Bi, Changfen
Liang, Yulu
Shen, Lijin
Tian, Shanshan
Zhang, Kai
Li, Yiliang
He, Xiwen
Chen, Langxing
Zhang, Yukui
Maltose-Functionalized Hydrophilic Magnetic Nanoparticles with Polymer Brushes for Highly Selective Enrichment of N-Linked Glycopeptides
title Maltose-Functionalized Hydrophilic Magnetic Nanoparticles with Polymer Brushes for Highly Selective Enrichment of N-Linked Glycopeptides
title_full Maltose-Functionalized Hydrophilic Magnetic Nanoparticles with Polymer Brushes for Highly Selective Enrichment of N-Linked Glycopeptides
title_fullStr Maltose-Functionalized Hydrophilic Magnetic Nanoparticles with Polymer Brushes for Highly Selective Enrichment of N-Linked Glycopeptides
title_full_unstemmed Maltose-Functionalized Hydrophilic Magnetic Nanoparticles with Polymer Brushes for Highly Selective Enrichment of N-Linked Glycopeptides
title_short Maltose-Functionalized Hydrophilic Magnetic Nanoparticles with Polymer Brushes for Highly Selective Enrichment of N-Linked Glycopeptides
title_sort maltose-functionalized hydrophilic magnetic nanoparticles with polymer brushes for highly selective enrichment of n-linked glycopeptides
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044954/
https://www.ncbi.nlm.nih.gov/pubmed/30023808
http://dx.doi.org/10.1021/acsomega.7b01788
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