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.
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Authors | R Laine, C C Sweeley, Y T Li, A Kisic, M M Rapport |
Journal | Journal of lipid research
(J Lipid Res)
Vol. 13
Issue 4
Pg. 519-24
(Jul 1972)
ISSN: 0022-2275 [Print] United States |
PMID | 5068000
(Publication Type: Journal Article)
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Chemical References |
- Cerebrosides
- Haptens
- Galactosamine
- Galactosidases
- Hexosaminidases
- Galactose
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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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