Institute for Research Management, Oita University.
Research Center for GLOBAL/LOCAL Infectious Diseases, Oita University.
Proc Jpn Acad Ser B Phys Biol Sci. 2023;99(6):155-172. doi: 10.2183/pjab.99.010.
Catalytic antibodies possess unique features capable of both recognizing and enzymatically degrading antigens. Therefore, they are more beneficial than monoclonal antibodies (mAbs). Catalytic antibodies exhibit the ability to degrade peptides, antigenic proteins, DNA, and physiologically active molecules. However, they have a significant drawback in terms of their production. The production of a desired catalytic antibody has extensive costs, in terms of time and effort. We herein describe an evolutionary method to produce a desired catalytic antibody via conversion of a general antibody by the deletion of Pro95, which resides in complementarity-determining region-3. As over thousands of mAbs have been produced since 1975, using the novel technology discussed herein, the catalytic feature cleaving the antigen can be conferred to the mAb. In this review article, we discussed in detail not only the role of Pro95 but also the unique features of the converted catalytic antibodies. This technique will accelerate research on therapeutic application of catalytic antibodies.
催化抗体具有独特的特性,既能识别又能酶解抗原。因此,它们比单克隆抗体(mAbs)更有益。催化抗体具有降解肽、抗原蛋白、DNA 和生理活性分子的能力。然而,它们在生产方面存在一个显著的缺点。生产所需的催化抗体需要大量的时间和精力。我们在这里描述了一种通过删除位于互补决定区 3 中的 Pro95 来将普通抗体转化为所需催化抗体的进化方法。自 1975 年以来已经产生了数千种 mAbs,使用本文讨论的新技术,可以将切割抗原的催化特性赋予 mAb。在这篇综述文章中,我们不仅详细讨论了 Pro95 的作用,还讨论了转化后的催化抗体的独特特性。这项技术将加速催化抗体治疗应用的研究。