Permethylation and tandem mass spectrometry of oligosaccharides having free hexosamine: analysis of the glycoinositol phospholipid anchor glycan from the scrapie prion protein

Anal Biochem. 1990 Nov 15;191(1):174-82. doi: 10.1016/0003-2697(90)90405-x.

Abstract

Permethylation of the glycan isolated from the glycoinositol phospholipid (GPI) anchor of the scrapie prion protein (PrPSc) trimethylates a free hexosamine to form a quarternary ammonium salt, substantially increasing the sensitivity for analysis by mass spectrometry. This derivatization induces specific fragmentation reactions in collision-induced dissociation spectra obtained on a four-sector tandem mass spectrometer, identifying the branching pattern of the PrPSc GPI glycan.

Publication types

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

MeSH terms

  • Glycolipids / analysis*
  • Glycosylphosphatidylinositols
  • Hexosamines / chemistry*
  • Methylation
  • Molecular Structure
  • Oligosaccharides / chemistry*
  • Phosphatidylinositols / analysis*
  • PrPSc Proteins
  • Prions / analysis*
  • Spectrum Analysis
  • Viral Proteins / analysis*
  • Viral Proteins / chemistry

Substances

  • Glycolipids
  • Glycosylphosphatidylinositols
  • Hexosamines
  • Oligosaccharides
  • Phosphatidylinositols
  • PrPSc Proteins
  • Prions
  • Viral Proteins