Akiba Hiroki, Takayanagi Kensuke, Kusano-Arai Osamu, Iwanari Hiroko, Hamakubo Takao, Tsumoto Kouhei
Center for Drug Design Research, National Institutes of Biomedical Innovation, Health and Nutrition, 7-6-8 Saito-Asagi, Ibaraki, Osaka, 567-0085, Japan.
Department of Bioengineering, School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8656, Japan.
Biotechnol Rep (Amst). 2020 Jan 11;25:e00418. doi: 10.1016/j.btre.2020.e00418. eCollection 2020 Mar.
Biparatopic fragment antibodies can overcome deficiencies in avidity of conventional antibody fragments. Here, we describe a technology for generating biparatopic antibodies through two-step targeting using a pair of polypeptides, SpyTag and SpyCatcher, that spontaneously react to form a covalent bond between antibody fragments. In this method, two antibody fragments, each targeting different epitopes of the antigen, are fused to SpyTag and to SpyCatcher. When the two polypeptides are serially added to the antigen, their proximity on the antigen results in covalent bond formation and generation of a biparatopic antibody. We validated the system with purified recombinant antigen. Results in antigen-overexpressing cells were promising although further optimization will be required. Because this strategy results in high-affinity targeting with a bipartite molecule that has considerably lower molecular weight than an antibody, this technology is potentially useful for diverse applications.
双表位片段抗体可以克服传统抗体片段亲和力不足的问题。在此,我们描述了一种通过两步靶向生成双表位抗体的技术,该技术使用一对多肽SpyTag和SpyCatcher,它们可自发反应在抗体片段之间形成共价键。在这种方法中,两个分别靶向抗原不同表位的抗体片段,分别与SpyTag和SpyCatcher融合。当将这两种多肽依次添加到抗原中时,它们在抗原上的接近会导致共价键形成并产生双表位抗体。我们用纯化的重组抗原验证了该系统。在抗原过表达细胞中的结果很有前景,不过仍需要进一步优化。由于该策略通过一种分子量比抗体低得多的双分子实现高亲和力靶向,因此该技术在多种应用中可能具有实用性。