Carter B G, Harris T N
Immunology. 1967 Jan;12(1):75-88.
Anti-azo benzene sulphonate antibodies were isolated from rabbit serum using two different methods in succession: first specific precipitation, and then specific absorption to a solid immunoadsorbent. The two purified preparations of antibody differed considerably in their ability to precipitate with antigen. It was found, however, that the non-precipitating antibody could largely be coprecipitated with antigen when mixed with precipitating antibody. Hapten binding experiments carried out on both preparations of antibody indicated that the κ values were of the same order of magnitude. The difference in method of preparation used was shown to have negligible effect on the hapten binding properties of the two antibodies. The important differences between the non-precipitating and precipitating antibodies were: (1) electrophoretic mobility, and (2) antigenic specificity. The precipitating antibody was identified as a γG-globulin, the non-precipitating variety as probably a γA-globulin. These results are compatible with the presence of a greater number of ionizable groups, i.e. potentially hydrophilic groups, on the non-precipitating antibody. The consequent higher molecular charge of the non-precipitating antibody may be an important factor in the failure of this antibody to precipitate with antigen.
首先是特异性沉淀,然后是对固体免疫吸附剂的特异性吸附。两种纯化的抗体制剂在与抗原沉淀的能力上有很大差异。然而,发现当与沉淀抗体混合时,非沉淀抗体在很大程度上可以与抗原共沉淀。对两种抗体制剂进行的半抗原结合实验表明,κ值处于相同的数量级。所用制备方法的差异对两种抗体的半抗原结合特性影响可忽略不计。非沉淀抗体和沉淀抗体之间的重要差异在于:(1)电泳迁移率,以及(2)抗原特异性。沉淀抗体被鉴定为γG球蛋白,非沉淀型可能是γA球蛋白。这些结果与非沉淀抗体上存在更多可电离基团(即潜在的亲水基团)相符。非沉淀抗体随之而来的更高分子电荷可能是该抗体不能与抗原沉淀的一个重要因素。