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Method | Open Access

Phenylboronic acid-functionalized magnetic nanoparticles for one-step saccharides enrichment and mass spectrometry analysis

Xiangdong Xue1Yuanyuan Zhao1Xu Zhang1Chunqiu Zhang1Anil Kumar1Xiaoning Zhang2Guozhang Zou1( )Paul C. Wang4Jinchao Zhang3Xing-Jie Liang1 ( )
CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety, National Center for Nanoscience and Technology, Beijing 100190, China
Laboratory of Pharmaceutics, School of Medicine, Tsinghua University, Beijing 100084, China
College of Chemistry & Environmental Science, Chemical Biology Key Laboratory of Hebei Province, Hebei University, Baoding 071002, China
Fu Jen Catholic University, Taipei 24205, China

Xiangdong Xue and Yuanyuan Zhao have contributed equally to this work.

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Abstract

In this work, 2-(2-aminoethoxy) ethanol-blocked phenylboronic acid-functionalized magnetic nanoparticles (blocked PMNPs) were fabricated for selective enrichment of different types of saccharides. The phenylboronic acid was designed for capturing the cis-diols moieties on saccharides molecules, and the 2-(2-aminoethoxy) ethanol can deplete the nonspecific absorption of peptides and proteins which always coexisted with saccharides. For mass spectrometry analysis, the PMNPs bound saccharides can be directly applied onto the MALDI plate with matrix without removing the PMNPs. By PMNPs, the simple saccharide (glucose) could be detected in pmol level. The complex saccharides can also be reliably purified and analyzed; 16 different N-glycans were successfully identified from ovalbumin, and the high-abundance N-glycans can be detected even when the ovalbumin was in very low concentration (2 μg). In human milk, ten different oligosaccharides were identified, and the lactose can still be detected when the human milk concentration was low to 0.01 μL.

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Biophysics Reports
Pages 61-70

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Cite this article:
Xue X, Zhao Y, Zhang X, et al. Phenylboronic acid-functionalized magnetic nanoparticles for one-step saccharides enrichment and mass spectrometry analysis. Biophysics Reports, 2015, 1(2): 61-70. https://doi.org/10.1007/s41048-015-0002-3

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Received: 18 January 2015
Accepted: 01 April 2015
Published: 14 July 2015
© The Author(s) 2015

This 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.