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1.
Bioorg Khim ; 24(6): 412-21, 1998 Jun.
Article in Russian | MEDLINE | ID: mdl-9702351

ABSTRACT

Surface-enhanced Raman scattering (SERS) spectroscopy was used to study the structure of carbohydrate chains in glycosylated forms of alpha 1-acid glycoprotein (AGP) and in pseudoglycoproteins obtained by transferring the carbohydrate chains of AGP to a polyacrylamide carrier. It was found that AGP-D glycoform and pseudoglycoproteins containing three or more glycans per molecule, which possess high immunomodulating activity, have a specific spatial organization of carbohydrate chains. This organization is maintained by the interaction of neighboring glycans with each other and does not depend on the nature of the carrier (whether it is polypeptide or polyacrylamide).


Subject(s)
Adjuvants, Immunologic/chemistry , Carbohydrates/chemistry , Orosomucoid/chemistry , Acrylic Resins/chemistry , Carbohydrate Sequence , Humans , Molecular Sequence Data , Peptides/chemistry , Protein Conformation , Spectrum Analysis, Raman/methods , Structure-Activity Relationship
2.
Bioorg Khim ; 23(11): 910-8, 1997 Nov.
Article in Russian | MEDLINE | ID: mdl-9518432

ABSTRACT

Neoglycoconjugates based on polyacrylamide and sialic acid with N-acetylneuraminic acid or sialooligosaccharides as side chains were studied by surface-enhanced Raman scattering (SERS) spectroscopy. It had previously been found that these polymers can effectively inhibit influenza virus adhesion. This study revealed the possibility to evaluate, based on the intensity of SERS signals, the overall availability for interaction and the conformational freedom of sialic acid residues in glycoconjugates. The dependence of these two factors on the structure and density of sialylated side chains was studied. The uniformity of distribution of sialylated side chains in conjugates was shown. Comparison of the results of the SERS spectroscopic study of the conjugates and the data on their inhibitory effect on the adhesion of specific strains of influenza virus allowed the identification of the conjugates for which the availability and conformational freedom of sialic acid are the main factors determining their inhibitory properties. A conclusion was also reached about the predominance of one of the mechanisms (competitive inhibition or steric stabilization) in the inhibitory properties of the specific conjugates.


Subject(s)
Glycoconjugates/chemistry , N-Acetylneuraminic Acid/chemistry , Oligosaccharides/chemistry , Acrylic Resins/chemistry , Glycoconjugates/pharmacology , Influenza A virus/drug effects , N-Acetylneuraminic Acid/pharmacology , Oligosaccharides/pharmacology , Spectrum Analysis, Raman , Structure-Activity Relationship
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