N-azidoacetylmannosamine-mediated chemical tagging of gangliosides

J Lipid Res. 2007 Jun;48(6):1417-21. doi: 10.1194/jlr.C700006-JLR200. Epub 2007 Mar 27.

Abstract

Peracetylated N-alpha-azidoacetylmannosamine (Ac(4)ManNAz) is metabolized by cells to CMP-azidosialic acid. It has been demonstrated previously that in this way azidosialic acid-containing glycoproteins are formed that can be labeled on the cell surface by a modified Staudinger ligation. Here, we first demonstrate that the same procedure also results in the formation of azidosialic acid-containing gangliosides. Deoxymannojirimycin, an inhibitor of N-glycan processing in proteins, decreases the total cell surface labeling in Jurkat cells by approximately 25%. Inhibition of ganglioside biosynthesis with N-[5-(adamantan-1-yl-methoxy)-pentyl]1-deoxynojirimycin reduces cell surface labeling by approximately 75%. In conclusion, exposure of cells to Ac(4)ManNAz allows in vivo chemical tagging of gangliosides.

MeSH terms

  • 1-Deoxynojirimycin / pharmacology
  • Azides / chemistry
  • Azides / metabolism*
  • Carbohydrate Metabolism / drug effects
  • Gangliosides / chemistry
  • Gangliosides / metabolism*
  • Glycoproteins / chemistry
  • Glycoproteins / metabolism
  • Hexosamines / chemistry
  • Hexosamines / metabolism*
  • Humans
  • Jurkat Cells
  • Oligosaccharides / chemistry
  • Oligosaccharides / metabolism

Substances

  • Azides
  • Gangliosides
  • Glycoproteins
  • Hexosamines
  • N-azidoacetylmannosamine
  • Oligosaccharides
  • 1-Deoxynojirimycin