Bioinformatics Institute, Agency for Science, Technology and Research (ASTAR), Singapore, Singapore.
p53 Laboratory, Agency for Science, Technology and Research (ASTAR), Singapore, Singapore.
Front Immunol. 2018 Mar 12;9:469. doi: 10.3389/fimmu.2018.00469. eCollection 2018.
Many therapeutic antibodies are humanized from animal sources. In the humanization process, complementarity determining region grafting is tedious and highly prone to failure. With seven known VH families, and up to six known κ VL families, there are choices aplenty. However, the functions of these families remain largely enigmatic. To study the role of these V-region families, we made 84 recombinant combinations of the various VH and VL family whole IgG1 variants of both Trastuzumab and Pertuzumab. We managed to purify 66 of these to investigate the biophysical characteristics: recombinant protein production, and both Her2 and FcγIIA binding. Our findings revealed combinations that showed improved recombinant antibody production and both antigen and receptor binding kinetics. These findings show the need to rethink antibodies as a whole protein, relooking of the functions of the antibody domains, and the need to include immunoglobulin receptor investigations for effective antibody therapeutics development.
许多治疗性抗体是从动物来源中进行人源化改造的。在人源化过程中,互补决定区的移植是繁琐的,并且非常容易失败。已知有七个 VH 家族,多达六个已知的 κ VL 家族,选择很多。然而,这些家族的功能在很大程度上仍然是神秘的。为了研究这些 V 区家族的作用,我们构建了 84 种重组组合,这些组合是曲妥珠单抗和帕妥珠单抗的各种 VH 和 VL 家族全 IgG1 变体。我们设法纯化了其中的 66 种,以研究其生物物理特性:重组蛋白的产生,以及 Her2 和 FcγIIA 的结合。我们的研究结果显示,一些组合显示出了改进的重组抗体生产能力,以及抗原和受体结合动力学。这些发现表明,需要重新思考整个蛋白质作为抗体,重新审视抗体结构域的功能,以及需要包括免疫球蛋白受体的研究,以有效开发抗体治疗药物。