Berger M
Biochemistry. 1975 Jun 3;14(11):2338-42. doi: 10.1021/bi00682a010.
Methods were developed for the coupling of biotin to bovine serum albumin and bovine gamma-globulin using a water-soluble carbodimide. The use of [14-C]biotin as a tracer allowed quantitation of the incorporation of biotin into the conjugates: 2.55 mol of biotin was incorporated per mol of gamma-globulin and 7-9 mol of biotin was incorporated per mol of serum albumin in different preparations. These conjugates were highly immunogenic in the rabbit and anti-bodies reactive with the biotinyl group itself could be detected by their ability to precipitate the heterologous biotinated carrier but not the unmodified heterologous carrier. There antisera rapidly inactivated transcarboxylase and pyruvate carboxylase and this inactivation could be blocked by pretreatment of the antisera with biotin or biocytin. Using enzyme inhibition to detect free antibody, the binding constant for biotin was found to be 5.0 x 10- minus 8 M and that for biocytin 3.5 x 10- minus 8 M.
已开发出使用水溶性碳二亚胺将生物素与牛血清白蛋白和牛γ球蛋白偶联的方法。使用[14-C]生物素作为示踪剂可对生物素掺入缀合物的情况进行定量:在不同制剂中,每摩尔γ球蛋白掺入2.55摩尔生物素,每摩尔血清白蛋白掺入7 - 9摩尔生物素。这些缀合物在兔体内具有高度免疫原性,并且通过它们沉淀异源生物素化载体而非未修饰异源载体的能力,可以检测到与生物素基团本身反应的抗体。这些抗血清能迅速使转羧酶和丙酮酸羧化酶失活,并且这种失活可以通过用生物素或生物胞素预处理抗血清来阻断。利用酶抑制来检测游离抗体,发现生物素的结合常数为5.0×10⁻⁸ M,生物胞素的结合常数为3.5×10⁻⁸ M。