Diakun K R, Yazawa S, Valenzuela L, Abbas S A, Matta K L
Immunol Invest. 1987 Apr;16(2):151-63. doi: 10.3109/08820138709030572.
Antibody to the carbohydrate moiety of T antigen was developed. The synthetic antigen (Gal beta 1----3 GalNAc alpha 1----OC6H4N = N-BSA) was prepared by coupling the diazonium salt of the disaccharide derivative Gal beta 1----3 GalNAc alpha 1----OC6H4NH2 (o) with bovine serum albumin. Specificity of the antibody produced was examined with structurally related synthetic saccharides using the enzyme immunoassay technique. The presence of a glycosyl group at 0-6 of either the Gal or the GalNAc residue of the disaccharide Gal beta 1----3 GalNAc did not prevent binding of the antisera to the saccharide moiety. However, the antisera did not bind either the trisaccharide moiety NeuAc2----3 Gal beta 1----3 GalNAc alpha 1----OC6H4NO2 (o) or GlcNAc beta 1----3 Gal beta 1----3 GalNAc alpha OBn. These observations indicate that antibody approach to the antigen is to the 0-3 side of the terminal galactose in the disaccharide Gal beta 1----3 GalNAc. We have also observed that the antibody prefers Gal beta 1----3 GalNAc alpha 1----to Gal beta 1----3 GalNAc beta 1----disaccharide derivatives in its binding capacity. The antibody was found to bind natural T antigen present on neuraminidase-treated red blood cells and, by immunohistochemical analysis, it was found to bind to naturally occurring T antigen on breast tumor cells.
制备了针对T抗原碳水化合物部分的抗体。通过将二糖衍生物Galβ1----3GalNAcα1----OC6H4NH2(邻位)的重氮盐与牛血清白蛋白偶联,制备了合成抗原(Galβ1----3GalNAcα1----OC6H4N = N-BSA)。使用酶免疫测定技术,用结构相关的合成糖类检测所产生抗体的特异性。二糖Galβ1----3GalNAc的Gal或GalNAc残基的0-6位存在糖基并不妨碍抗血清与糖类部分的结合。然而,抗血清既不与三糖部分NeuAc2----3Galβ1----3GalNAcα1----OC6H4NO2(邻位)也不与GlcNAcβ1----3Galβ1----3GalNAcαOBn结合。这些观察结果表明,抗体与抗原结合的部位是二糖Galβ1----3GalNAc中末端半乳糖的0-3侧。我们还观察到,抗体在结合能力上更倾向于Galβ1----3GalNAcα1----而非Galβ1----3GalNAcβ1----二糖衍生物。发现该抗体能与神经氨酸酶处理的红细胞上存在的天然T抗原结合,并且通过免疫组织化学分析发现,它能与乳腺肿瘤细胞上天然存在的T抗原结合。