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Localization of Multiple <i>O</i>-Linked Glycans Exhibited in Isomeric Glycopeptides by Hot Electron Capture Dissociation

Takashi Baba, Zoe Zhang, Suya Liu, Lyle Burton, Pavel Ryumin, J. Leblanc

2022Journal of Proteome Research33 citationsDOI

Abstract

We describe a method to obtain a comprehensive profile of multiple glycosylations in glycopeptide isoforms. We detected a wide range of abundances of various O-glycoforms in isomeric glycopeptides using hot electron capture dissociation (hot ECD) in liquid chromatography–tandem mass spectrometry. To capture low abundant glycosylated species, a prototype of a ZenoTOF 7600 system incorporating an efficient electron-activated dissociation device to perform hot ECD was operated in targeted or scheduled high-resolution multiple reaction monitoring workflows. In addition, Zeno trap pulsing was activated to enhance the sensitivity of the time-of-flight mass spectrometer. Sixty-nine O-glycopeptides of the long O-glycopeptides in tryptic bovine fetuin digest were obtained with a relative abundance range from 100 to 0.2%, which included sialylated glycans with Neu5Ac and Neu5Gc.

Topics & Concepts

GlycopeptideGlycanChemistryDissociation (chemistry)ChromatographyBiochemistryOrganic chemistryGlycoproteinAntibioticsGlycosylation and Glycoproteins ResearchCarbohydrate Chemistry and SynthesisRNA and protein synthesis mechanisms
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