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Structure of the O-Glycosidically Linked Carbohydrate Units of Fetuin
Open accessAbstract
Fetuin isolated from fetal calf serum was shown to contam 3 carbohydrate units which are attached to serine and threonine residues on the peptide chain and are distinct from the 3 asparagine-linked heteropolysaccharides previously reported to occur in this protein.The 0-glycosidically linked saccharide units were obtained as reduced oligosaccharides after alkaline borohydride treatment of fetuin and as glycopeptides subsequent to pronase digestion of this protein.Gel filtration and Dowex 1 chromatography of the oligosaccharides resulted in the isolation of a tri-and a tetrasaccharide which were made up of sialic acid, galactose, and N-acetylgalactosaminitol residues and could be converted after selective removal of the sialic acid to the same disaccharide (galactosyl-N-acetylgalactosaminitol).Studies employing periodate oxidation and glycosidase digestion indicated that the structure of the tetrasaccharide was N-acetylneuraminyl-(2 -+3) -P-D -galactopyranosyl-(l -+3)[N-acetylneuraminyl-(2 -+6)]-N-acetylgalactosaminiitol and that the trisaccharide differed only by the absence of the sialyl residue linked to the N-acetylgalactosaminitol.Glycopeptides containing the alkali-labile carbohydrate units were purified on Sephadex and diethylaminoethylcellulose columns.In this manner peptides distinguished by a high proline content and containing 1 tetrasaccharide, 1 trisaccharide, or 2 trisaccharides were obtained.Alkaline sulfite treatment of these glycopeptides indicated that 2 serine and 1 threonine residue in each fetuin molecule is involved in the attachment of carbohydrate units.The tetrasaccharide was found to be linked only to serine while attachment of trisaccharide units involved a serine and a threonine residue which were located in close proximity in the peptide chain.Smith periodate degradation of sialic acid-free glycopeptides resulted in removal of the galactose and yielded a product from which complete release of N-acetylgalactosamine
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Cited by
The purification, composition, and specificity of the anti-T lectin from peanut (Arachis hypogaea).
Lotan, R., Skutelsky, E., Danon, D., & Sharon, N. (1975) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)40790-4 · Cited by 939
Structural determinants of Ricinus communis agglutinin and toxin specificity for oligosaccharides
Baenziger, J. U., & Fiete, D. (1979) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)83586-x · Cited by 476
Parkos, C. A., Allen, R. A., Cochrane, C. G., & Jesaitis, A. J. (1987) · Journal of Clinical Investigation · doi:10.1172/jci113128 · Cited by 455
Wang, W. C., & Cummings, R. D. (1988) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)68821-0 · Cited by 451
Influence of the Carbohydrate Moiety on the Stability of Glycoproteins
Wang, C., Eufemi, M., Turano, C., & Giartosio, A. (1996) · Biochemistry · doi:10.1021/bi9517704 · Cited by 344
Metadata
- Authors
- Spiro, R. G., & Bhoyroo, V. D.
- Venue
- Journal of Biological Chemistry
- Publisher
- Elsevier BV
- Published
- 1974-09
- Volume
- 249
- Issue
- 18
- Pages
- 5704-5717
- ISSN
- 0021-9258 (ISSN-L)
- OpenAlex
- W1897055678
- Cited by
- 631
- References
- 0
- FWCI
- 8.62
- Type
- journal article
- Language
- en
- Open access
- hybrid
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- Spiro, R. G., & Bhoyroo, V. D. (1974). Structure of the O-Glycosidically Linked Carbohydrate Units of Fetuin. Journal of Biological Chemistry. https://doi.org/10.1016/s0021-9258(20)79875-3
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