Specific Identification of Glycoproteins Bearing the Tn Antigen in Human Cells

Angew Chem Int Ed Engl. 2017 Jun 12;56(25):7107-7111. doi: 10.1002/anie.201702191. Epub 2017 May 17.

Abstract

Glycoproteins contain a wealth of valuable information regarding the development and disease status of cells. In cancer cells, some glycans (such as the Tn antigen) are highly up-regulated, but this remains largely unknown for glycoproteins with a particular glycan. Herein, an innovative method combining enzymatic and chemical reactions was first designed to enrich glycoproteins with the Tn antigen. Using synthetic glycopeptides with O-GalNAc (the Tn antigen) or O-GlcNAc, we demonstrated that the method is selective for glycopeptides with O-GalNAc and can distinguish between these two modifications. The diagnostic ions from the tagged O-GalNAc further confirmed the effectiveness of the method and confidence in the identification of glycopeptides with the Tn antigen by mass spectrometry. Using this method, we identified 96 glycoproteins with the Tn antigen in Jurkat cells. The method can be extensively applied in biological and biomedical research.

Keywords: MS-based proteomics; Tn antigen; glycoproteins; hydrazide chemistry; specific identification.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Acetylgalactosamine / chemistry
  • Acylation
  • Antigens, Tumor-Associated, Carbohydrate / metabolism*
  • Glycopeptides / chemistry
  • Glycopeptides / metabolism*
  • Glycoproteins / chemistry
  • Glycoproteins / metabolism*
  • Glycosylation
  • Humans
  • Jurkat Cells
  • Mass Spectrometry / methods*

Substances

  • Antigens, Tumor-Associated, Carbohydrate
  • Glycopeptides
  • Glycoproteins
  • Tn antigen
  • Acetylgalactosamine