Pauillac S, Naar J, Branaa P, Chinain M
CNRS URA 359, Département d'Immunologie, Institut Pasteur, Paris, France.
J Immunol Methods. 1998 Nov 1;220(1-2):105-14. doi: 10.1016/s0022-1759(98)00148-3.
A rapid, simple and low cost procedure for preparing minute amount of hapten-protein conjugates was developed using 4-acetyl benzoic acid (ABA) and two other closely related small chromophoric haptens. The amide bond-generating mixed anhydride method of Erlanger was modified to promote conjugation to various proteins (bovine serum albumin, ovalbumin, casein and hemocyanin) or to a synthetic homopolymer (Poly-DL-lysine). The key process in this synthesis is the use of a reversed micellar medium allowing strong carrier haptenization as determined by spectrophotometric measurement at characteristic hapten absorption peaks. This coupling procedure is applicable to as little hapten material as 0.2 micromol and is disclosed to be most valuable for other rare lipid haptens which pose analytical problem in biological fluids and matrices. Specific mice polyclonal antibodies were produced following multiple intraperitoneal injections of (ABA)23-BSA conjugate as revealed by indirect and competitive ELISA. Calculated KD for the interaction of the antibodies with free ABA was found to be 5 X 10(-5)M.
利用4-乙酰苯甲酸(ABA)和其他两种密切相关的小发色半抗原,开发了一种快速、简单且低成本的制备微量半抗原-蛋白质缀合物的方法。对埃尔朗格生成酰胺键的混合酸酐法进行了改进,以促进与各种蛋白质(牛血清白蛋白、卵清蛋白、酪蛋白和血蓝蛋白)或合成均聚物(聚-DL-赖氨酸)的缀合。该合成中的关键步骤是使用反胶束介质,通过在特征性半抗原吸收峰处的分光光度测量确定,可实现强烈的载体半抗原化。这种偶联方法适用于低至0.2微摩尔的半抗原材料,并且对于在生物流体和基质中存在分析问题的其他稀有脂质半抗原而言具有极高价值。通过间接和竞争性ELISA发现,多次腹腔注射(ABA)23-BSA缀合物后产生了特异性小鼠多克隆抗体。计算得出抗体与游离ABA相互作用的解离常数(KD)为5×10(-5)M。