ZIC-cHILIC-Based StageTip for Simultaneous Glycopeptide Enrichment and Fractionation toward Large-Scale N-Sialoglycoproteomics
Yi‐Ju Chen, Ta-Chi Yen, Yu‐Hsien Lin, Yanlin Chen, Kay‐Hooi Khoo, Yu‐Ju Chen
Abstract
and ZIC-HILIC, respectively. To the best of our knowledge, the result with 2742 sialoglycopeptides among 7367 unique glycopeptides and 166 glycans from 2434 N-glycosites of 1118 glycoproteins (Byonic score > 100) provides one of the deepest glycoproteomic profiles in single-cell type. Without the immunoprecipitation step, the large-scale glycoproteomic atlas also reveals site-specific glycosylation of many druggable receptor proteins, such as EGFR, MET, ERBB2, ERBB3, AXL, and IGF1R. The demonstrated high enrichment specificity and identification depth show that stepwise ZIC-cHILIC is an efficient method to explore the under-represented sialoglycoproteome.
Topics & Concepts
ChemistryGlycopeptideChromatographyGlycosylationFractionationGlycanHydrophilic interaction chromatographyElutionGlycoproteinBiochemistryHigh-performance liquid chromatographyAntibioticsGlycosylation and Glycoproteins ResearchGenomics and Phylogenetic StudiesCarbohydrate Chemistry and Synthesis