Synthesis of the branched form of erythroglycan by Friend GM 979 erythroleukemic cells

T. Kaizu, S. J. Turco, J. S. Rush, R. A. Laine

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8 Scopus citations


Mouse GM979 erythroleukemic cells were found to synthesize the branched form of erythroglycan, a large polylactosamine structure known to be attached to band 3 and possibly to other proteins on human erythrocytes. Total protein-derived oligosaccharides from GM979 cells, labeled metabolically with [3H]glucosamine, [3H]mannose, or [3H]galactose, were prepared by hydrazinolysis after extracting the lipids. The 3H-labeled oligosaccharides were fractionated on Sephadex G-50 revealing 10-25% of each labeled product as a high molecular weight fraction (M(r)=10,000). Digestion of this [3H]glucosamine fraction with endo-β-galactosidase from Escherichia freundii, specific for the repeating structure of Galβ(1→4)GlcNAcβ(1→3), resulted in the following four products upon Bio-Gel P-2 Gel filtration; 1) a disaccharide with the structure GlcNAcβ(1→3)Gal,2) a trisaccharide with the structure Galβ(1→4)GlcNAcβ(1→3)βGal,3) a tetrasaccharide with the sequence Fucα(1 → 2)Galβ(1 → 4)GlcNacβ(1→3)Gal, and 4) a large complex fragment which contained mannose, glucosamine, galactose, and fucose (presumably the protein linkage region). Methylation linkage analysis of the large complex fraction shows mainly the presence of 4-substituted and terminal N-acetylglucosamine; 3,6-substituted, 6-substituted, 2-substituted, and 2,3-substituted galactose. The GM979 cell erythroglycan is only 30% susceptible to endo-β-galactosidase degradation probably because of the branched galactose residues, whereas the linear form of erythroglycan from human K562 cells is 60% susceptible. The branched residues in GM979 cell saccharides indicate that this mouse cell line bears an arborized erythroglycan-like glycopeptide similar to those found on human adult erythrocytes, and thus may be a source for the enzyme which transfers an N-acetylglucosamine residue to a 3-linked galactose to form a 3,6-disubstituted galactose.

Original languageEnglish
Pages (from-to)8272-8276
Number of pages5
JournalJournal of Biological Chemistry
Issue number14
StatePublished - 1982

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology


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