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• W2019296527 abstract "The coupling of the diazotization product of p-aminophenyl-β-d-galactopyranoside with the synthetic polypeptide antigen p(l-Glu, l-Tyr)-p-dl-Ala-p-l-Lys resulted in a conjugate which elicited in rabbits antibodies with galactose specificity. While the total amount of antibodies formed was much smaller than that formed by a similar galactose derivative of bovine serum albumin, the galactose specificity in the synthetic conjugate system was much higher than in the protein conjugate system. In order to avoid linkage of sugar derivatives to synthetic polypeptides through tyrosine, glucose was bound to p(l-Glu, l-Tyr)-p-dl-Ala-p-l-Lys and to the non-antigenic p-dl-Ala-p-l-Lys by making use of O-(tetra-O-acetyl-β-d-glucopyranosyl)-N-carboxy-l-serine anhydride. Antibodies with glucose specificity were obtained upon immunization with p-d-Glc-l-Ser-p(l-Glu, l-Tyr)-p-dl-Ala-p-l-Lys, but no immune response was detected in rabbits injected with two samples of p-d-Glc-l-Ser-p-dl-Ala-p-l-Lys. As was to be expected, a monosaccharide attached to protein contributes to serological specificity but it does not convert the non-antigenic p-dl-ALA-p-l-Lys into an immunogen." @default.
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• W2019296527 date "1966-03-01" @default.
• W2019296527 modified "2023-10-15" @default.
• W2019296527 title "Synthesis and antigenic properties of sugar-polypeptide conjugates" @default.
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• W2019296527 doi "https://doi.org/10.1016/0019-2791(66)90293-x" @default.
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