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J. Biol. Chem., Vol. 263, Issue 35, 18716-18725, 12, 1988
GK Ostrander, SB Levery, HL Eaton, ME Salyan, S Hakomori and EH Holmes
We have previously reported on carbohydrate structures of the major acidic
glycosphingolipids from the liver of the English sole, Parophrys vetulus
(Ostrander, G. K., Levery, S. B., Hakomori, S., and Holmes, E. H. (1988) J.
Biol. Chem. 263, 3103-3110). We have now isolated four major neutral
glycosphingolipids from English sole liver. They have been characterized by
1H nuclear magnetic resonance spectroscopy, methylation analysis, and by
fast atom bombardment-mass spectrometry. In addition to neutral
glycosphingolipids with known structures (CMH, lactosylceramide, and Gg3),
a major polar neutral glycosphingolipid was isolated and characterized as
having the following novel structure: (formula; see text) The compound
represents a novel hybrid of neolacto- , ganglio-, and iso-globo-series
glycosphingolipid structures, a combination not previously encountered.
Furthermore, the linkage Fuc alpha 1----3GalNac has not been previously
reported for a glycosphingolipid. The relationship of these structural
elements to known glycoconjugates is discussed.
Isolation and characterization of four major neutral glycosphingolipids from the liver of the English sole (Parophrys vetulus). Presence of a novel branched lacto-ganglio-iso-globo hybrid structure
Pacific Northwest Research Foundation, Seattle, Washington 98122.
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