Isomer-Specific LC/MS and LC/MS/MS Profiling of the Mouse Serum N-Glycome Revealing a Number of Novel Sialylated N-Glycans

被引:47
作者
Hua, Serenus [1 ,2 ]
Jeong, Ha Neul [1 ]
Dimapasoc, Lauren M. [3 ]
Kang, Inae [1 ]
Han, Chanyoung [1 ]
Choi, Jong-Soon [1 ,4 ]
Lebrilla, Carlito B. [3 ]
An, Hyun Joo [1 ,2 ]
机构
[1] Chungnam Natl Univ, Grad Sch Analyt Sci & Technol, Taejon, South Korea
[2] Chungnam Natl Univ, Canc Res Inst, Taejon, South Korea
[3] Univ Calif Davis, Dept Chem, Davis, CA 95616 USA
[4] Korea Basic Sci Inst, Div Life Sci, Taejon, South Korea
基金
新加坡国家研究基金会;
关键词
MASS-SPECTROMETRY; SIALIC-ACID; STRUCTURAL-ANALYSIS; IDENTIFICATION; MODEL; ANNOTATION; EXPRESSION; PROTEOMICS;
D O I
10.1021/ac400195h
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Mice are the premier mammalian models for studies of human physiology and disease, bearing extensive biological similarity to humans with far fewer ethical, economic, or logistic complications To facilitate glycornic studies based on the mouse model, we comprehensively profiled the mouse serum N-glycome using isomer specific nano-LC/MS and -LC/MS/MS. N-Glycans were identified by accurate mass MS and structurally elucidated by MS/MS. Porous graphitized carbon nano-LC was able to separate out nearly 300 N-linked glycan compounds (including isomers) from just over 100 distinct N-linked glycan compositions. Additional MS/MS structural analysis was performed on a number of novel N-glycans, revealing the structural characteristics of modifications such as dehydration, O-acetylation, and lactylation. Experimental findings were combined with known glycobiology to generate a theoretical library of all biologically possible mouse serum N-glycan compositions. The library may be used for automated identification of complex mixtures of mouse N-glycans, with possible applications to a wide range of mouse-related research endeavors, including pharmaceutical drug development and biomarker discovery.
引用
收藏
页码:4636 / 4643
页数:8
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