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Automated interpretation of tandem mass spectra of N-linked oligosaccharides obtained from matrix-assisted laser desorption/ionization.

机译:自动解释从基质辅助激光解吸/电离获得的N-连接寡糖的串联质谱。

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摘要

Oligosaccharides associated with proteins are known to give these molecules specific conformations and functions. The analysis of proteins would thus not be complete without studying glycans. However, high-throughput techniques in proteomics will soon overwhelm the current capacity of methods if no automation is incorporated into glycomics. The StrOligo (for structure of oligosaccharides) algorithm developed for this purpose will be discussed here.; Simulated tandem mass spectra were used to define the limits of the algorithm. Experimental tandem mass spectra were then acquired to validate the algorithm using a hybrid quadrupole-time-of-flight (QqTOF) instrument with a matrix-assisted laser desorption ionization (MALDI) source. The samples were composed of N-linked oligosaccharides from monoclonal antibody IgG, recombinant beta interferon, bovine fetuin and human integrin. Glycans were detached by enzymatic deglycosylation and labelled at the reducing end.; The algorithm first builds a relationship tree, explaining each observed loss of monosaccharide moiety and relating corresponding peaks to one another. The algorithm then analyzes the tree and proposes possible compositions and structures from combinations of adduct and fragment ion types. A score, which reflects agreement with experimental results, is then given to each proposed structure. The program then shows the structures found and the score they obtained and labels relevant peaks in the experimental mass spectrum using a modified nomenclature for the structure with the highest score.; The usefulness of the algorithm has been demonstrated by assigning structures to glycan populations of several glycoproteins. The algorithm has also been used to assign glycan populations to a specific glycosylation site of integrin. Analyses were completed in less than two minutes for the most complex structures, which is a substantial improvement over manual interpretation, which can take a few hours. StrOligo is thus a good step in the direction of high-throughput glycomics.
机译:已知与蛋白质相关的寡糖赋予这些分子特定的构象和功能。因此,如果不研究聚糖,蛋白质的分析将是不完整的。但是,如果没有将自动化技术整合到糖组学中,蛋白质组学中的高通量技术将很快使现有方法的能力不堪重负。在此将讨论为此目的开发的StrOligo(用于寡糖的结构)算法。模拟串联质谱用于定义算法的限制。然后获取实验串联质谱图,以使用带有矩阵辅助激光解吸电离(MALDI)源的混合四极杆飞行时间(QqTOF)仪器验证算法。样品由单克隆抗体IgG,重组β干扰素,牛胎球蛋白和人整联蛋白的N-连接寡糖组成。通过酶促去糖基化分离聚糖并在还原端标记。该算法首先建立关系树,解释每个观察到的单糖部分的损失,并将相应的峰相互关联。然后,该算法对树进行分析,并根据加合物和碎片离子类型的组合提出可能的成分和结构。然后为每个建议的结构提供一个分数,该分数反映了与实验结果的一致性。然后,程序将显示找到的结构及其获得的分数,并使用具有最高分数的结构的修改名称来标记实验质谱中的相关峰。通过将结构分配给几种糖蛋白的聚糖种群,已经证明了该算法的有效性。该算法也已用于将聚糖群体分配给整联蛋白的特定糖基化位点。对于最复杂的结构,分析可以在不到两分钟的时间内完成,这比人工解释要花费数小时的时间有了实质性的改进。因此,StrOligo是朝着高通量糖组学方向迈出的重要一步。

著录项

  • 作者

    Ethier, Martin.;

  • 作者单位

    University of Manitoba (Canada).;

  • 授予单位 University of Manitoba (Canada).;
  • 学科 Chemistry Analytical.
  • 学位 Ph.D.
  • 年度 2005
  • 页码 133 p.
  • 总页数 133
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

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