[Synthesis of N-glycoproteins with a native type of carbohydrate-peptide bond].

Autor: Likhosherstov LM, Piskarev VE, Derevitskaia VA, Kochetkov NK
Jazyk: ruština
Zdroj: Bioorganicheskaia khimiia [Bioorg Khim] 1990 Jan; Vol. 16 (1), pp. 124-6.
Abstrakt: Reaction of beta-oligoglycosylamines obtained from carbohydrate chains of N-glycoproteins (ovalbumin, ovomucoid, riboflavin-binding glycoprotein from hen egg white, and asialofetuin) with bovine serum albumin, lysozyme, and poly(L-Asp) in presence of water-soluble carbodiimide gave rise to a series of glycoconjugates, modelling natural N-glycoproteins. Carbohydrate-peptide bond was shown to be of N-glycosylamide type with participation of Asp and Glu residues. The method allows one to obtain synthetic N-glycoproteins from oligomannoside, complex and hybrid oligosaccharide chains, and may find application both in biochemistry and biotechnology for improvement of physico-chemical properties of unglycosylated proteins.
Databáze: MEDLINE