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On the structure of cytolipin R, a ceramide tetrahexoside hapten from rat lymphosarcoma.

Abstract
Cytolipin R, a ceramide tetrahexoside isolated from rat lymphosarcoma, was studied by sequential hydrolysis with specific glycosidases which revealed the anomeric configurations of the glycosidic bonds. Sugar linkages were established by combined gas-liquid chromatography and mass spectrometry of the partially methylated alditol acetates prepared after permethylation and hydrolysis of the intact lipid. Results indicated the structure of cytolipin R to be N-acetylgalactosaminyl(beta1-->3)galactosyl(alpha1-->3) galactosyl(beta1-->4)glucosyl ceramide. Cytolipin K (globoside I) differs in having a -galactosyl(alpha1-->4)galactosyl- internal linkage, and this difference must account for the immunological differences between cytolipin K and cytolipin R.
AuthorsR Laine, C C Sweeley, Y T Li, A Kisic, M M Rapport
JournalJournal of lipid research (J Lipid Res) Vol. 13 Issue 4 Pg. 519-24 (Jul 1972) ISSN: 0022-2275 [Print] United States
PMID5068000 (Publication Type: Journal Article)
Chemical References
  • Cerebrosides
  • Haptens
  • Galactosamine
  • Galactosidases
  • Hexosaminidases
  • Galactose
Topics
  • Alkylation
  • Animals
  • Cerebrosides (analysis, isolation & purification)
  • Chemical Phenomena
  • Chemistry
  • Chromatography, Gas
  • Computers
  • Galactosamine (analysis)
  • Galactose (analysis)
  • Galactosidases
  • Haptens
  • Hexosaminidases
  • Isomerism
  • Lymphoma, Non-Hodgkin (immunology)
  • Mass Spectrometry
  • Plants (enzymology)
  • Rats
  • Sarcoma, Experimental (immunology)
  • Structure-Activity Relationship

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