LC-MS/MS of isomeric N-and O-glycopeptides on mesoporous graphitized carbon column

糖肽 化学 色谱法 胎球蛋白 聚糖 糖基化 洗脱 糖蛋白 生物化学 抗生素
作者
Oluwatosin Emmanuel Daramola,Sakshi Gautam,Cristian D. Gutierrez Reyes,Mojibola Fowowe,Sherifdeen Bamidele Onigbinde,Judith Ijeoma Nwaiwu,Yehia S. Mechref
出处
期刊:Analytica Chimica Acta [Elsevier BV]
卷期号:1317: 342907-342907 被引量:12
标识
DOI:10.1016/j.aca.2024.342907
摘要

The study of glycopeptides is associated with challenges regarding the microheterogeneity of different isomeric glycans occupying the same glycosylation sites in glycoproteins. It is immensely valuable to perform both qualitative and quantitative site-specific glycosylation analysis of glycopeptide isomers due to their link to several diseases. Achieving isomeric separation of glycopeptides is particularly challenging due to the low abundance of glycopeptides as well as inefficient ionization. Although some methods have demonstrated the isomeric separation of glycopeptides, a more efficient nanoflow-based stationary phase is needed for the isomeric separation of both N- and O-glycopeptides. In this study, the separation of N- and O-glycopeptide isomers at 75°C was achieved with an in-house packed 1cm long mesoporous graphitized carbon (MGC) column. Different gradient compositions of the optimized mobile phase for the separating permethylated glycans on MGC column were tested, and we observed efficient separation of N- and O-glycopeptide isomers at a gradient elution time of 120 min. After achieving the isomeric separation of sialylated glycopeptides from model glycoproteins derived from bovine fetuin, the separation of isomeric glycopeptides derived from asialofetuin, α-1 glycoprotein and human blood serum were also demonstrated. Furthermore, the developed method for the separation of isomeric N- and O-glycopeptide on MGC column showed high reproducibility over three months. We observed an average retention time shift of 1 min and consistent resolution of separated peaks throughout three months. MGC column can serve as an efficient tool for obtaining the isomeric separation of N- and O-glycopeptide from complex biological samples in future studies. This will enable a more profound understanding of the roles played by isomeric N- and O-glycopeptide in important biological processes and their correlations to various disease progressions.
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