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Updated: Mar 28, 2026

Mass Spectrometric Analysis of Glycosphingolipid Antigens
Published on: April 16, 2013
Ethyl Esterification for MALDI-MS Analysis of Protein Glycosylation
Karli R Reiding1, Emanuela Lonardi1, Agnes L Hipgrave Ederveen1
1Center for Proteomics and Metabolomics, Leiden University Medical Center, Leiden, The Netherlands.
Abstract:
Ethyl esterification is a technique for the chemical modification of sialylated glycans, leading to enhanced stability when performing matrix-assisted laser desorption/ionization (MALDI)-mass spectrometry (MS), as well as allowing the efficient detection of both sialylated and non-sialylated glycans in positive ion mode. In addition, the method shows specific reaction products for α2,3- and α2,6-linked sialic acids, leading to an MS distinguishable mass difference. Here, we describe the ethyl esterification protocol for 96 glycan samples, including enzymatic N-glycan release, the aforementioned ethyl esterification, glycan enrichment, MALDI target preparation, and the MS(/MS) measurement.
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