Identification of substituted sites on MUC5AC mucin motif peptides after enzymatic O-glycosylation combining beta-elimination and fixed-charge derivatization

Rapid Commun Mass Spectrom. 2002;16(1):27-34. doi: 10.1002/rcm.532.

Abstract

A strategy for determination of O-glycosylation site(s) in glycopeptides has been developed using model compounds obtained by enzymatic glycosylation (by human GaNTase-T2 isoform) on peptides derived from the human MUC5AC mucin tandem repeat motif. The beta-elimination-addition reaction (using dimethylamine and concomitantly ethanethiol) on the formerly glycosylated sites through a Michael-type condensation produced efficient deglycosylation with appropriate chemical modification. After N-terminal derivatization by a phosphonium group, peptide sequencing was then carried out by nanospray tandem mass spectrometry experiments. The highly predictable fragmentation pathways of these fixed-charge phosphonium derivatives enable straightforward recognition of glycosylation site(s) based on the mass increment of +44 Da for originally glycosylated threonine compared to the mass of fragments containing nonglycosylated residues.

MeSH terms

  • Amino Acid Sequence
  • Catalysis
  • Dimethylamines
  • Glycopeptides / analysis*
  • Glycosylation
  • Humans
  • Molecular Sequence Data
  • Mucins / chemistry*
  • Spectrometry, Mass, Electrospray Ionization
  • Tandem Repeat Sequences

Substances

  • Dimethylamines
  • Glycopeptides
  • Mucins
  • dimethylamine