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Generation of scFv specific to human VEGFR-3 from the neutralizing mAb BDD073

机译:由中和单克隆抗体BDD073产生对人VEGFR-3特异的scFv

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In our previous study, we have produced a neutralizing mAb of vascular endothelial growth factor receptor 3 (VEGFR-3), specifically BDD073, which could inhibit angiogenesis in the CAM model. However, the clinical application of BDD073 is restricted due to its mouse origin, which might cause human anti-mouse antibody reactions. Herein, we generated functional recombinant single-chain variable fragments (scFv) from mAb BDD073 producing mouse hybridoma cells. The scFv gene containing variable regions of heavy and light chains of BDD073 was cloned into an expression vector with trx tag and expressed in Escherichia coli BL21 (DE3). The recombinant scFv was purified and refolded with Ni-NTA agarose metal affinity column. The bacterially expressed scFv showed moderate potency and specificity to the human VEGFR-3. It may serve as a potential candidate of anti-VEGFR3 treatment for biotechnological and therapeutic applications.
机译:在我们之前的研究中,我们产生了中和性的血管内皮生长因子受体3(VEGFR-3)mAb,特别是BDD073,它可以抑制CAM模型中的血管生成。但是,由于BDD073的小鼠来源,其临床应用受到了限制,这可能会引起人类抗小鼠抗体反应。本文中,我们从产生mAb BDD073的小鼠杂交瘤细胞中生成了功能重组单链可变片段(scFv)。将含有BDD073重链和轻链可变区的scFv基因克隆到带有trx标签的表达载体中,并在大肠杆菌BL21(DE3)中表达。纯化重组scFv,并用Ni-NTA琼脂糖金属亲和柱重折叠。细菌表达的scFv显示出对人VEGFR-3的中等效力和特异性。它可作为抗VEGFR3治疗生物技术和治疗应用的潜在候选者。

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