Identification and Relative-Quantification of Glycans by Matrix-Assisted Laser Desorption/Ionization In-Source Decay with Hydrogen Abstraction

被引:17
作者
Asakawa, Daiki [1 ,2 ,3 ]
Smargiasso, Nicolas [1 ,2 ]
De Pauw, Edwin [1 ,2 ]
机构
[1] Univ Liege, Dept Chem, B-4000 Liege, Belgium
[2] Univ Liege, Mass Spectrometry Lab, GIGA R, B-4000 Liege, Belgium
[3] Yokohama City Univ, Mass Spectrometry Lab, Grad Sch Nanobiosci, Kanazawa Ku, Yokohama, Kanagawa 232, Japan
基金
日本学术振兴会;
关键词
COLLISION-INDUCED DISSOCIATION; NEGATIVE-ION MODE; UV-MALDI-TOF; C-ALPHA-C; MASS-SPECTROMETRY; POSTSOURCE DECAY; FRAGMENTATION; OLIGOSACCHARIDES; MS; PEPTIDES;
D O I
10.1021/ac3014737
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The use of specific matrixes allows enhancing the scope of in-source decay (ISD) applications in matrix-assisted laser desorption/ionization (MALDI) thanks to the specificity of analyte-matrix chemistry. The use of an oxidizing matrix, 5-nitrosalicylic acid (5-NSA), for MALDI-ISD of glycans is shown to promote fragmentation pathways involving radical precursors. Both glycosidic and cross-ring cleavages are promoted by hydrogen abstraction from hydroxyl group of glycans by 5-NSA molecules. Cross-ring cleavage ions are potentially useful in linkage analysis, one of the most critical steps of glycan characterization. Moreover, we show here that isobaric glycans could be distinguished by structure specific ISD ions and that the molar ratio of glycan isomers in the mixture can be estimated from their fragment ions abundance. The use of 5-NSA also opens the possibility to perform pseudo-MS3 analysis of glycans. Therefore, MALDI-ISD with 5-NSA is a useful method for identification of glycans and semiquantitative analysis of mixture of glycan isomers.
引用
收藏
页码:7463 / 7468
页数:6
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