首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Designed synthesis of ultra-hydrophilic sulfo-functionalized metal-organic frameworks with a magnetic core for highly efficient enrichment of the N-linked glycopeptides
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Designed synthesis of ultra-hydrophilic sulfo-functionalized metal-organic frameworks with a magnetic core for highly efficient enrichment of the N-linked glycopeptides

机译:设计了具有磁芯的超亲水磺官能化金属 - 有机框架的合成,用于高效富集N键合糖肽

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Highly efficient extraction and enrichment of the N-linked glycopeptides from complex biological samples before mass spectrometry analysis remains important but challenging, due to the low abundance and suppression by proteins and salts. Herein, a facile route to an ultra-hydrophilic metal-organic frameworks (MOFs)-functionalized magnetic nanoparticle (Fe3O4@PDA@Zr-SO3H) was proposed. The as-prepared MOFs was endowed with excellent and unique properties, such as excellent hydrophilicity, ultrahigh surface area, and strong magnetic responsiveness. By virtue of these properties and based on hydrophilic interaction, Fe3O4@PDA@Zr-SO3H exhibited outstanding sensitivity and selectivity, remarkable recyclability and stability towards N-linked glycopeptide enrichment. In deep, a total of 177 N-linked glycopeptides, assigned to 85 different glycoproteins, were identified from the healthy human serum after treated with the Fe3O4@PDA@Zr-SO3H. These results confirmed that our strategy offered a promising platform for preparing hydrophilic metal-organic framework-functionalized magnetic nanoparticles for glycosylation analysis by mass spectrometry analysis. (C) 2017 Elsevier B.V. All rights reserved.
机译:在质谱分析之前,从复杂的生物样品中高效提取和富集来自复杂的生物样品,仍然是重要的,但由于蛋白质和盐的较低和抑制而苛刻。这里,提出了一种用于超亲水金属 - 有机骨架(MOF) - 官能化磁性纳米粒子(Fe3O4 @ PDA Zr-So3H)的容易途径。制备的制造MOF是具有优异和独特的性质,例如优异的亲水性,超高表面积和强磁反应性。借助于这些性质并基于亲水性相互作用,Fe3O4 @ PDA @ Zr-SO3H表现出出色的敏感性和选择性,显着的再循环性和朝向N-连接的糖肽富集的稳定性。在用Fe3O4 @ PDA Zr-So3H处理后,在健康的人血清中鉴定出总共177个N型连接的糖肽,分配给85种不同的糖蛋白。这些结果证实,我们的策略为通过质谱分析进行了用于制备用于糖基化分析的亲水金属 - 有机骨架官能化磁性纳米粒子的有希望的平台。 (c)2017年Elsevier B.V.保留所有权利。

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