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N-glycans released from glycoproteins using a commercial kit and comprehensively analyzed with a hypothetical database

机译:使用商业试剂盒从糖蛋白释放的N-聚糖并通过假设数据库进行全面分析

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摘要

The glycosylation of proteins is responsible for their structural and functional roles in many cellular activities. This work describes a strategy that combines an efficient release, labeling and liquid chromatography-mass spectral analysis with the use of a comprehensive database to analyze N-glycans. The analytical method described relies on a recently commercialized kit in which quick deglycosylation is followed by rapid labeling and cleanup of labeled glycans. This greatly improves the separation, mass spectrometry (MS) analysis and fluorescence detection of N-glycans. A hypothetical database, constructed using GlycResoft, provides all compositional possibilities of N-glycans based on the common sugar residues found in N-glycans. In the initial version this database contains >8,700 N-glycans, and is compatible with MS instrument software and expandable. N-glycans from four different well-studied glycoproteins were analyzed by this strategy. The results provided much more accurate and comprehensive data than had been previously reported. This strategy was then used to analyze the N-glycans present on the membrane glycoproteins of gastric carcinoma cells with different degrees of differentiation. Accurate and comprehensive N-glycan data from those cells was obtained efficiently and their differences compared corresponding to their differentiation states. Thus, the novel strategy developed greatly improves accuracy, efficiency and comprehensiveness of N-glycan analysis.
机译:蛋白质的糖基化负责其在许多细胞活动中的结构和功能作用。这项工作描述了一种策略,该策略结合了有效的释放,标记和液相色谱-质谱分析以及使用综合数据库来分析N-聚糖的方法。所描述的分析方法依赖于最近商业化的试剂盒,其中快速去糖基化之后是快速标记和纯化标记的聚糖。这极大地改善了N-聚糖的分离,质谱(MS)分析和荧光检测。使用GlycResoft构建的假设数据库可根据N-聚糖中常见的糖残基提供N-聚糖的所有组成可能性。在初始版本中,该数据库包含> 8,700个N-聚糖,并且与MS仪器软件兼容并且可扩展。通过这种策略分析了来自四种研究充分的糖蛋白的N-聚糖。结果提供的数据比以前报告的更加准确和全面。然后将该策略用于分析存在不同分化程度的胃癌细胞膜糖蛋白上存在的N-聚糖。有效地获得了来自那些细胞的准确和全面的N-聚糖数据,并将它们的差异与它们的分化状态相对应。因此,开发出的新策略极大地提高了N-聚糖分析的准确性,效率和综合性。

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