Identification of Isomeric N-Glycans by Conformer Distribution Fingerprinting using Ion Mobility Mass Spectrometry

被引:18
作者
Torano, Javier Sastre [1 ]
Aizpurua-Olaizola, Oier [1 ,5 ]
Wei, Na [2 ]
Li, Tiehai [2 ]
Unione, Luca [1 ]
Jimenez-Oses, Gonzalo [3 ]
Corzana, Francisco [4 ]
Somovilla, Victor J. [1 ]
Falcon-Perez, Juan M. [5 ]
Boons, Geert-Jan [1 ,2 ]
机构
[1] Univ Utrecht, Utrecht Inst Pharmaceut Sci, Dept Chem Biol & Drug Discovery, Utrecht, Netherlands
[2] Univ Georgia, Complex Carbohydrate Res Ctr, Athens, GA 30602 USA
[3] Basque Res & Technol Alliance BRTA, Ctr Cooperat Res Biosci CIC BioGUNE, Bizkaia Technol Pk,Bldg 801A, Derio 48160, Spain
[4] Univ La Rioja, Ctr Invest Sintesis Quim, Dept Quim, Logrono 26006, Spain
[5] CIBERehd, Exosomes Lab, CIC BioGUNE, Derio, Spain
关键词
carbohydrates; chemo-enzymatic synthesis; conformations; ion mobility spectrometry; mass spectrometry; molecular dynamics; COLLISION CROSS-SECTIONS; CHEMOENZYMATIC SYNTHESIS; GLYCOSYLATION; SIALYLGLYCOPEPTIDE; OLIGOSACCHARIDES;
D O I
10.1002/chem.202004522
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Glycans possess unparalleled structural complexity arising from chemically similar monosaccharide building blocks, configurations of anomeric linkages and different branching patterns, potentially giving rise to many isomers. This level of complexity is one of the main reasons that identification of exact glycan structures in biological samples still lags behind that of other biomolecules. Here, we introduce a methodology to identify isomeric N-glycans by determining gas phase conformer distributions (CDs) by measuring arrival time distributions (ATDs) using drift-tube ion mobility spectrometry-mass spectrometry. Key to the approach is the use of a range of well-defined synthetic glycans that made it possible to investigate conformer distributions in the gas phase of isomeric glycans in a systematic manner. In addition, we have computed CD fingerprints by molecular dynamics (MD) simulation, which compared well with experimentally determined CDs. It supports that ATDs resemble conformational populations in the gas phase and offer the prospect that such an approach can contribute to generating a library of CCS distributions (CCSDs) for structure identification.
引用
收藏
页码:2149 / 2154
页数:6
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