Journal
TALANTA
Volume 221, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.talanta.2020.121382
Keywords
Purification; Two-dimensional liquid chromatography; Natural N-Glycan; Negative ion fragmentation; Glycan microarray
Categories
Funding
- National High Technology Research and Development Program of China [2012AA020203]
- National Natural Science Foundation of China [21135005]
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A purification strategy based on two-dimensional hydrophilic interaction liquid chromatography and porous graphitized carbon chromatography was established to obtain neutral N-glycan standards from natural sources. The purified N-glycans with defined structures, purity, and amounts were successfully assembled on glass slides, demonstrating the potential of the strategy in glycan library expansion and functional glycomics. The detailed structures of the N-glycan compounds were verified through negative ion tandem MS analysis, allowing for identification of isomeric and terminal fine structures.
Glycan microarray for studying carbohydrate-protein interactions requires diverse classes of well-defined glycan standards. In this study, a purification strategy was established based on two-dimensional hydrophilic interaction liquid chromatography and porous graphitized carbon chromatography (HILIC x PGC) for the acquisition of neutral N-glycan standards from natural source. A total of thirty-one N-glycan compounds including seven pairs of isomers with the amounts from 0.7 to 230.0 nmol were isolated from ovalbumin as the model glycoconjugate. The purified N-glycans covered high-mannose, hybrid as well as multi-antenna asymmetric complex types. The purity of majority of these N-glycans was higher than 90%. Detailed structures of the N-glycan compounds were verified via negative ion tandem MS analysis, in which specific diagnostic ions including D- and E -ions were used to identify isomeric and terminal fine structures. The tag-free glycan compounds with well-defined structures, purity and amounts were finally assembled on the glass slide through neoglycolipid technology. Micmarray binding assay of purified glycans with WGA lectin indicated the potential of the established strategy in glycan library expansion and functional glycomics.
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