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通过电子激发解离进行详细的聚糖结构表征。

Detailed glycan structural characterization by electronic excitation dissociation.

机构信息

Department of Biochemistry, Boston University , 670 Albany St. Suite 504, Boston, Massachusetts 02118, United States.

出版信息

Anal Chem. 2013 Nov 5;85(21):10017-21. doi: 10.1021/ac402886q. Epub 2013 Oct 9.

Abstract

The structural complexity and diversity of glycans parallel their multilateral functions in living systems. To better understand the vital roles glycans play in biological processes, it is imperative to develop analytical tools that can provide detailed glycan structural information. This was conventionally achieved by multistage tandem mass spectrometry (MS(n)) analysis using collision-induced dissociation (CID) as the fragmentation method. However, the MS(n) approach lacks the sensitivity and throughput needed to analyze complex glycan mixtures from biological sources, often available in limited quantities. We define herein the critical parameters for a recently developed fragmentation technique, electronic excitation dissociation (EED), which can yield rich structurally informative fragment ions during liquid chromatographic (LC)-MS/MS analysis of glycans. We further demonstrate that permethylation, reducing end labeling and judicious selection of the metal charge carrier, can greatly facilitate spectral interpretation. With its high sensitivity, throughput, and compatibility with online chromatographic separation techniques, EED appears to hold great promise for large-scale glycomics studies.

摘要

糖链在生命系统中的功能多样,其结构也复杂多样。为了更好地理解糖链在生物过程中所起的重要作用,开发能够提供详细糖链结构信息的分析工具势在必行。传统上,这是通过多级串联质谱(MS(n))分析,采用碰撞诱导解离(CID)作为碎片化方法来实现的。然而,MS(n) 方法缺乏分析生物来源的复杂糖混合物所需的灵敏度和通量,而这些混合物通常数量有限。我们在此定义了一种最近开发的碎片化技术——电子激发解离(EED)的关键参数,该技术在糖链的液相色谱-质谱/质谱(LC-MS/MS)分析中可以产生丰富的结构信息碎片离子。我们还进一步证明,通过全甲基化、还原末端标记和明智地选择金属电荷载体,可以极大地促进谱图解析。EED 具有高灵敏度、高通量以及与在线色谱分离技术的兼容性,因此在大规模糖组学研究中似乎具有广阔的前景。

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