Abstract
Conjugates consisting of methyl 2( p-azobenzamido)2-deoxy-α- d-glucopyranoside and methyl 2( p-azobenzamido)-2-β- d-glucopyranoside coupled to bovine serum albumin were used as synthetic antigens. Rabbits immunized with artificial antigen provided specific anti-methyl α-glucosaminide or anti-methyl β-glucosaminide anti-hapten sera. Quantitative hapten inhibition was employed to elucidate the specificity of anti-hapten combining sites and to evaluate some structural and configurational features contributing to the immunochemical interaction with the antibody. It is shown that the configuration at the anomeric carbon atom makes a major contribution to the immunochemical specificity of the anti-hapten antibodies against α- and β-methyl glycosides.
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