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Production and characterization of monoclonal anti-idiotypic antibodyexhibiting a catalytic activity similar to carboxypeptidase A

机译:具有与羧肽酶A相似的催化活性的单克隆抗独特型抗体的生产和表征

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摘要

A new approach for producing catalytic antiidiotypic antibody was developed. A monoclonal anti-idiotypic antibody which was induced against carboxypeptidase A (CPA) showed the catalytic activity similar to the original antigen. The activity of the catalytic antibody was in investigated. Rabbits were immunized by bovine pancreas carboxypeptidase A. The antiserum was purified and used as antigen to immunize BALB/c mice to induce monoclonal anti-idiotypic antibodies. Screened for enzymatic activities, the monoclonal antibody 32C3 showed esterase activity. The hydrolysis of hippuryl-DL-phenyllactic acid by McAb 32C3 followed the enzymatic kinetics. In our experimental system, K-cat value was 0.0123 min(-1) and K(m)( )was 0.04 M. The acceleration rate was 1750 times compared to the rate of self-hydrolysis of the substrate.This hydrolysis reaction can be competitively inhibited by hydrocinnamic acid. This method could be effective to obtain catalytic antibodies with the characters close to natural enzymes.
机译:开发了一种生产催化抗独特型抗体的新方法。针对羧肽酶A(CPA)诱导的单克隆抗独特型抗体显示出与原始抗原相似的催化活性。研究了催化抗体的活性。用牛胰腺羧肽酶A对家兔进行免疫。纯化抗血清并将其用作抗原以免疫BALB / c小鼠以诱导单克隆抗独特型抗体。筛选酶活性,单克隆抗体32C3显示酯酶活性。 McAb 32C3对马尿酰-DL-苯基乳酸的水解遵循酶动力学。在我们的实验系统中,K-cat值为0.0123 min(-1),K(m)()为0.04 M.与底物的自水解速率相比,加速速率为1750倍。氢肉桂酸竞争性抑制。该方法可能有效地获得具有接近天然酶特征的催化抗体。

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