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The role of Antibody Vκ Framework 3 region towards Antigen binding: Effects on recombinant production and Protein L binding

机译:抗体Vκ框架的作用3区域朝向抗原结合:对重组生产和蛋白质L的作用

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摘要

Abstract Antibody research has traditionally focused on heavy chains, often neglecting the important complementary role of light chains in antibody formation and secretion. In the light chain, the complementarity-determining region 3 (VL-CDR3) is specifically implicated in disease states. By modulating VL-CDR3 exposure on the scaffold through deletions in the framework region 3 (VL-FWR3), we further investigated the effects on secretion in recombinant production and antigen binding kinetics. Our random deletions of two residues in the VL-FWR3 of a Trastuzumab model showed that the single deletions could impact recombinant production without significant effect on Her2 binding. When both the selected residues were deleted, antibody secretion was additively decreased, and so was Her2 binding kinetics. Interestingly, we also found allosteric effects on the Protein L binding site at VL-FWR1 elicited by these deletions in VL- FWR3. Together, these findings demonstrate the importance of light chain FWR3 in antigen binding, recombinant production, and antibody purification using Protein L.
机译:摘要抗体研究传统上集中在重链上,往往忽视轻链在抗体形成和分泌中的重要互补作用。在轻链中,互补确定区域3(VL-CDR3)特异性地涉及疾病状态。通过在框架区域3(VL-FWR3)中的缺失通过缺失调节VL-CDR3暴露,我们进一步研究了重组生产和抗原结合动力学中分泌的影响。我们在曲妥珠单抗模型的VL-FWR3中的两种残留的随机缺失表明,单次缺失可能会影响重组生产,而不会对HER2结合显着影响。当缺失两个所选残留物时,抗体分泌加剧降低,HER2结合动力学也是如此。有趣的是,我们还发现在VL-FWR3中引发的VL-FWR1蛋白L粘合位点对蛋白质L末端位点的构想作用。这些研究结果在一起证明了使用蛋白质L的抗原结合,重组生产和抗体纯化的轻链FWR3的重要性。

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