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Novel data analysis tool for semiquantitative LC-MS-MS~2 profiling of N-glycans

机译:用于N-聚糖半定量LC-MS-MS〜2分析的新型数据分析工具

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Despite recent technical advances in glycan analysis, the rapidly growing field of glycomics still lacks methods that are high throughput and robust, and yet allow detailed and reliable identification of different glycans. LC-MS-MS~2 methods have a large potential for glycan analysis as they enable separation and identification of different glycans, including structural isomers. The major drawback is the complexity of the data with different charge states and adduct combinations. In practice, manual data analysis, still largely used for MALDI-TOF data, is no more achievable for LC-MS-MS~2 data. To solve the problem, we developed a glycan analysis software GlycanID for the analysis of LC-MS-MS~2 data to identify and profile glycan compositions in combination with existing proteomic software. IgG was used as an example of an individual glycoprotein and extracted cell surface proteins of human fibroblasts as a more complex sample to demonstrate the power of the novel data analysis approach. N-glycans were isolated from the samples and analyzed as permethylated sugar alditols by LC-MS-MS~2, permitting semiquantitative glycan profiling. The data analysis consisted of five steps: 1) extraction of LC-MS features and MS~2 spectra, 2) mapping potential glycans based on feature distribution, 3) matching the feature masses with a glycan composition database and de novo generated compositions, 4) scoring MS~2 spectra with theoretical glycan fragments, and 5) composing the glycan profile for the identified glycan compositions. The resulting N-glycan profile of IgG revealed 28 glycan compositions and was in good correlation with the published IgG profile. More than 50 glycan compositions were reliably identified from the cell surface N-glycan profile of human fibroblasts. Use of the GlycanID software made relatively rapid analysis of complex glycan LC-MS-MS~2 data feasible. The results demonstrate that the complexity of glycan LC-MS-MS~2 data can be used as an asset to increase the reliability of the identifications.
机译:尽管在聚糖分析方面有最新的技术进步,但是快速增长的糖组学领​​域仍缺乏高通量和鲁棒性的方法,但仍可以对不同的聚糖进行详细而可靠的鉴定。 LC-MS-MS〜2方法具有广泛的聚糖分析潜力,因为它们能够分离和鉴定包括结构异构体在内的不同聚糖。主要缺点是具有不同电荷状态和加合物组合的数据的复杂性。在实践中,对于LC-MS-MS〜2数据而言,手动数据分析仍然广泛用于MALDI-TOF数据。为了解决该问题,我们开发了一种聚糖分析软件GlycanID来分析LC-MS-MS〜2数据,结合现有的蛋白质组学软件来识别和分析聚糖成分。 IgG用作单个糖蛋白的实例,人成纤维细胞的提取细胞表面蛋白作为更复杂的样品来证明这种新型数据分析方法的强大功能。从样品中分离出N-聚糖,并通过LC-MS-MS〜2分析为过甲基化糖醛糖醇,可进行半定量聚糖分析。数据分析包括五个步骤:1)提取LC-MS特征和MS〜2光谱,2)根据特征分布绘制潜在的聚糖,3)将特征质量与聚糖成分数据库匹配并从头产生的成分,4 )用理论上的聚糖片段对MS〜2光谱评分,以及5)组成已鉴定出的聚糖成分的聚糖谱。 IgG的所得N-聚糖谱显示28种聚糖成分,并与已发表的IgG谱良好相关。从人成纤维细胞的细胞表面N-聚糖谱可靠地鉴定出超过50种聚糖组合物。使用GlycanID软件可以相对快速地分析复杂的聚糖LC-MS-MS〜2数据。结果表明,聚糖LC-MS-MS〜2数据的复杂性可以作为资产来提高识别的可靠性。

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