Effective Assignment of α2,3/α2,6-Sialic Acid Isomers by LC-MS/MS-Based Glycoproteomics

Angew Chem Int Ed Engl. 2018 Jul 20;57(30):9320-9324. doi: 10.1002/anie.201803540. Epub 2018 Jun 20.

Abstract

Distinct structural changes of the α2,3/α2,6-sialic acid glycosidic linkages on glycoproteins are of importance in cancer biology, inflammatory diseases, and virus tropism. Current glycoproteomic methodologies are, however, not amenable toward high-throughput characterization of sialic acid isomers. To enable such assignments, a mass spectrometry method utilizing synthetic model glycopeptides for the analysis of oxonium ion intensity ratios was developed. This method was successfully applied in large-scale glycoproteomics, thus allowing the site-specific structural characterization of sialic acid isomers.

Keywords: glycopeptides; glycosylation; isomers; mass spectrometry; sialic acids.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carbohydrate Conformation
  • Chromatography, Liquid
  • Proteomics*
  • Sialic Acids / chemistry*
  • Stereoisomerism
  • Tandem Mass Spectrometry

Substances

  • Sialic Acids