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J. Biol. Chem., Vol. 259, Issue 8, 4866-4877, 04, 1984
SR Hull, RA Laine, T Kaizu, I Rodriguez and KL Carraway
Structures of the principal O-glycosides from the major cell surface
sialoglycoprotein (ASGP-1) of the MAT-B1 and MAT-C1 ascites sublines of the
13762 rat mammary adenocarcinoma have been determined. Oligosaccharitols
were released by alkaline borohydride treatments of ASGP-1 and purified by
gel filtration, DEAE-Sephadex ion exchange chromatography, and high
performance liquid chromatography. On the basis of carbohydrate
composition, methylation analysis, periodate oxidation, and exoglycosidase
digestion, the five major oligosaccharides released by mild alkaline
borohydride were assigned the following structures: Component II-3: (NeuAc
alpha 2----3Gal beta 1- ---4GlcNAc beta 1----6)Ga 1 NAcOH(3----1 betaGa 1
3----2 alpha NeuAc) III-2a: (Ga 1 beta 1----4G1cNAc beta 1----6)Ga 1
NAcOH(3----1 beta Ga 1 3----2 alpha NeuAc) III-2c: (Ga 1 alpha 1----3Ga 1
beta 1----4G1cNAc beta 1----6) Ga 1 NAcOH(3----1 beta Ga 1 3----2 alpha
NeuAc) IV-1a: (Ga 1 beta 1----4G 1 cNAc beta 1----6)Ga 1 NAcOH(3----1 beta
Ga 1) IV-1c: (Ga 1 alpha 1----3Ga 1 beta 1----4G 1 cNAc beta 1----6) Ga 1
NAcOH(3---- 1 beta Ga 1) Fucosylated derivatives of III-2a, IV-1a, and
IV-1c were found in smaller amounts with the fucose tentatively assigned to
the 2- position of the lactosamine galactose. Components II-3, III-2a, and
the fucosylated derivative of III-2A were found in both MAT-B1 and MAT-C1
sublines. The alpha-galactosides were found in detectable quantities only
in subline MAT-B1. Oligosaccharides from MAT-C1 cells were enriched in
sialic acid when compared to those from MAT-B1 cells. These results suggest
that the 13762 ascites sublines, which bear different oligosaccharides,
will provide models useful for the investigation of mechanisms regulating
the expression of structures of the larger O- linked oligosaccharides.
Structures of the O-linked oligosaccharides of the major cell surface sialoglycoprotein of MAT-B1 and MAT-C1 ascites sublines of the 13762 rat mammary adenocarcinoma
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