Hydrazide Functionalized Core–Shell Magnetic Nanocomposites for Highly Specific Enrichment of N-Glycopeptides

IF 8.2 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY
Liting Liu, Meng Yu, Ying Zhang, Changchun Wang*, Haojie Lu*
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引用次数: 111

Abstract

In view of the biological significance of glycosylation for human health, profiling of glycoproteome from complex biological samples is highly inclined toward the discovery of disease biomarkers and clinical diagnosis. Nevertheless, because of the existence of glycopeptides at relatively low abundances compared with nonglycosylated peptides and glycan microheterogeneity, glycopeptides need to be highly selectively enriched from complex biological samples for mass spectrometry analysis. Herein, a new type of hydrazide functionalized core–shell magnetic nanocomposite has been synthesized for highly specific enrichment of N-glycopeptides. The nanocomposites with both the magnetic core and the polymer shell hanging high density of hydrazide groups were prepared by first functionalization of the magnetic core with polymethacrylic acid by reflux precipitation polymerization to obtain the Fe3O4@poly(methacrylic acid) (Fe3O4@PMAA) and then modification of the surface of Fe3O4@PMAA with adipic acid dihydrazide (ADH) to obtain Fe3O4@poly(methacrylic hydrazide) (Fe3O4@PMAH). The abundant hydrazide groups toward highly specific enrichment of glycopeptides and the magnetic core make it suitable for large-scale, high-throughput, and automated sample processing. In addition, the hydrophilic polymer surface can provide low nonspecific adsorption of other peptides. Compared to commercially available hydrazide resin, Fe3O4@PMAH improved more than 5 times the signal-to-noise ratio of standard glycopeptides. Finally, this nanocomposite was applied in the profiling of N-glycoproteome from the colorectal cancer patient serum. In total, 175 unique glycopeptides and 181 glycosylation sites corresponding to 63 unique glycoproteins were identified in three repeated experiments, with the specificities of the enriched glycopeptides and corresponding glycoproteins of 69.6% and 80.9%, respectively. Because of all these attractive features, we believe that this novel hydrazide functionalized core–shell magnetic nanocomposite will shed new light on the profiling of N-glycoproteome from complex biological samples in high throughput.

Abstract Image

酰肼功能化核壳磁性纳米复合材料用于n -糖肽的高特异性富集
鉴于糖基化对人类健康的生物学意义,从复杂的生物样品中分析糖蛋白组非常倾向于发现疾病生物标志物和临床诊断。然而,由于与非糖基化肽相比,糖肽的丰度相对较低,而且多糖的微异质性,因此需要从复杂的生物样品中高度选择性地富集糖肽以进行质谱分析。本文合成了一种新型的酰肼功能化核壳磁性纳米复合材料,用于n -糖肽的高特异性富集。采用回流沉淀聚合的方法,先用聚甲基丙烯酸对磁性核进行功能化,得到Fe3O4@poly(甲基丙烯酸)(Fe3O4@PMAA),再用己二酸二肼(ADH)对Fe3O4@PMAA表面进行改性,得到Fe3O4@poly(甲基丙烯酸肼)(Fe3O4@PMAH),制备了磁性核和聚合物壳同时悬挂高密度肼基团的纳米复合材料。丰富的酰肼基团对糖肽和磁芯的高特异性富集使其适合大规模、高通量和自动化样品处理。此外,亲水性聚合物表面可以提供低非特异性吸附其他肽。与市售的肼树脂相比,Fe3O4@PMAH提高了标准糖肽的5倍以上的信噪比。最后,将该纳米复合材料应用于结直肠癌患者血清中n -糖蛋白组的分析。通过3次重复实验,共鉴定出175个独特的糖肽和对应63个独特糖蛋白的181个糖基化位点,富集的糖肽和对应糖蛋白的特异性分别为69.6%和80.9%。由于所有这些吸引人的特点,我们相信这种新型的酰肼功能化核壳磁性纳米复合材料将为复杂生物样品的n -糖蛋白组高通量分析提供新的思路。
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来源期刊
ACS Applied Materials & Interfaces
ACS Applied Materials & Interfaces 工程技术-材料科学:综合
CiteScore
16.00
自引率
6.30%
发文量
4978
审稿时长
1.8 months
期刊介绍: ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.
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