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国际数据分析工作组:用于培养细胞定量糖组学的稳定同位素标记的代谢掺入。

IDAWG: Metabolic incorporation of stable isotope labels for quantitative glycomics of cultured cells.

作者信息

Orlando Ron, Lim Jae-Min, Atwood James A, Angel Peggi M, Fang Meng, Aoki Kazuhiro, Alvarez-Manilla Gerardo, Moremen Kelley W, York William S, Tiemeyer Michael, Pierce Michael, Dalton Stephen, Wells Lance

机构信息

Complex Carbohydrate Research Center, Department of Biochemistry and Molecular Biology, University of Georgia, Athens, 30602, USA.

出版信息

J Proteome Res. 2009 Aug;8(8):3816-23. doi: 10.1021/pr8010028.

Abstract

Robust quantification is an essential component of comparative -omic strategies. In this regard, glycomics lags behind proteomics. Although various isotope-tagging and direct quantification methods have recently enhanced comparative glycan analysis, a cell culture labeling strategy, that could provide for glycomics the advantages that SILAC provides for proteomics, has not been described. Here, we report the development of IDAWG, Isotopic Detection of Aminosugars With Glutamine, for the incorporation of differential mass tags into the glycans of cultured cells. In this method, culture media containing amide-(15)N-Gln is used to metabolically label cellular aminosugars with heavy nitrogen. Because the amide side chain of Gln is the sole source of nitrogen for the biosynthesis of GlcNAc, GalNAc, and sialic acid, we demonstrate that culturing mouse embryonic stems cells for 72 h in the presence of amide-(15)N-Gln media results in nearly complete incorporation of (15)N into N-linked and O-linked glycans. The isotopically heavy monosaccharide residues provide additional information for interpreting glycan fragmentation and also allow quantification in both full MS and MS/MS modes. Thus, IDAWG is a simple to implement, yet powerful quantitative tool for the glycomics toolbox.

摘要

可靠的定量分析是比较组学策略的重要组成部分。在这方面,糖组学落后于蛋白质组学。尽管最近各种同位素标记和直接定量方法增强了聚糖的比较分析,但尚未描述一种能为糖组学提供与SILAC为蛋白质组学所提供优势相同的细胞培养标记策略。在此,我们报告了IDAWG(谷氨酰胺介导的氨基糖同位素检测)的开发,用于将差异质量标签掺入培养细胞的聚糖中。在该方法中,含有酰胺 -(15)N - 谷氨酰胺的培养基用于用重氮代谢标记细胞氨基糖。由于谷氨酰胺的酰胺侧链是GlcNAc、GalNAc和唾液酸生物合成的唯一氮源,我们证明在酰胺 -(15)N - 谷氨酰胺培养基存在下培养小鼠胚胎干细胞72小时会导致(15)N几乎完全掺入N - 连接和O - 连接的聚糖中。同位素重的单糖残基为解释聚糖片段化提供了额外信息,并且还允许在全质谱和串联质谱模式下进行定量。因此,IDAWG是一种易于实施且功能强大的糖组学定量工具。

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