Capillary Electrophoresis-Electrospray Ionization-Mass Spectrometry for Quantitative Analysis of Glycans Labeled with Multiplex Carbonyl-Reactive Tandem Mass Tags

被引:76
|
作者
Zhong, Xuefei [1 ]
Chen, Zhengwei [2 ]
Snovida, Sergei [3 ]
Liu, Yan [4 ]
Rogers, John C. [3 ]
Li, Lingjun [1 ,2 ]
机构
[1] Univ Wisconsin, Sch Pharm, Madison, WI 53705 USA
[2] Univ Wisconsin, Dept Chem, Madison, WI 53706 USA
[3] Thermo Fisher Sci, Thermo Sci Pierce Prot Res, Rockford, IL 61105 USA
[4] Xiamen Univ, Sch Chem & Chem Engn, Xiamen 361005, Peoples R China
关键词
N-LINKED GLYCANS; PROTEIN GLYCOSYLATION; LIQUID-CHROMATOGRAPHY; HIGH-SENSITIVITY; STRUCTURAL-CHARACTERIZATION; INDUCED FLUORESCENCE; ION MOBILITY; GLYCOMICS; QUANTIFICATION; IDENTIFICATION;
D O I
10.1021/acs.analchem.5b01835
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Recently developed carbonyl-reactive aminoxy tandem mass tag (aminoxyTMT) reagents enable multiplexed characterization and quantitative comparison of structurally complex glycans between different biological samples. Compared to some previously reported isotopic labeling strategies for glycans, the use of the aminoxyTMT method features a simple labeling procedure, excellent labeling efficiency, and reduced spectral complexity at the MS' level. Presence of the tertiary amine functionality in the reporter region of the aminoxyTMT labels leads to increased ionization efficiency of the labeled glycans thus improving electrospray ionization (ESI)-mass spectrometry (MS) detection sensitivity. The use of the labeling reagent also makes electrophoretic separation of the labeled neutral and acidic glycans feasible. In this work, we characterized the ESI and collision induced dissociation (CID) behavior of the aminoxyTMT-labeled neutral and sialylated glycans. For the high-mannose N-glycans and small sialylated oligosaccharides, CID fragmentation of [M + Na + H](2+) provides the most informative MS2 spectra for both quantitative and qualitative analysis. For complex N-glycans, MS3 of the protonated Y-1(H) ion can be used for relative quantification without interference from the HexNAc fragments. Online capillary electrophoresis (CE)-ESI-MS/MS analyses of multiplexed aminoxyTMT-labeled human milk oligosaccharides (HMOs) and different types of N-glycans released from glycoprotein standards were demonstrated. Improved resolution and quantification accuracy of the labeled HMO isomers was achieved by coupling CE with traveling wave ion mobility (TWIM)-CID-MS/MS. N-Glycans released from human serum protein digests were labeled with six-plex aminoxyTMT and subjected to CE-ESI-MS/pseudo-MS3 analysis, which demonstrated the potential utility of this glycan relative quantification platform for more complex biological samples.
引用
收藏
页码:6527 / 6534
页数:8
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