4.8 Article

Effective Assignment of alpha 2,3/alpha 2,6-Sialic Acid Isomers by LC-MS/MS-Based Glycoproteomics

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 57, Issue 30, Pages 9320-9324

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201803540

Keywords

glycopeptides; glycosylation; isomers; mass spectrometry; sialic acids

Funding

  1. Inga-Britt and Arne Lundberg research foundation
  2. Knut and Alice Wallenberg foundation
  3. Swedish research council [8266]
  4. Kempe foundation
  5. Deutsche Forschungsgemeinschaft (DFG) [WE 4751/2-1]
  6. Fonds der Chemischen Industrie [Li 184/01]
  7. Ministerium fur Kultur und Wissenschaft des Landes Nordrhein-Westfalen
  8. Regierende Burgermeister von Berlininkl
  9. Sahlgrenska University Hospital

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Distinct structural changes of the alpha 2,3/alpha 2,6-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.

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