Maltose-Functionalized Hydrophilic Magnetic Nanoparticles with Polymer Brushes for Highly Selective Enrichment of N-Linked Glycopeptides
Author(s) -
Changfen Bi,
Yulu Liang,
Lijin Shen,
Shanshan Tian,
Kai Zhang,
Yiliang Li,
Xiwen He,
Langxing Chen,
Yukui Zhang
Publication year - 2018
Publication title -
acs omega
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.779
H-Index - 40
ISSN - 2470-1343
DOI - 10.1021/acsomega.7b01788
Subject(s) - polyethylenimine , chemistry , chromatography , glycoproteomics , detection limit , selectivity , polymer , glycopeptide , magnetic nanoparticles , bovine serum albumin , combinatorial chemistry , nanoparticle , nanotechnology , biochemistry , materials science , organic chemistry , transfection , catalysis , gene , antibiotics
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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