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Transient expression of a tumor-specific single-chain fragment and a chimeric antibody in tobacco leaves

机译:烟叶中肿瘤特异性单链片段和嵌合抗体的瞬时表达

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摘要

To evaluate the expression of different forms of a tumor-specific antibody in plants, we adapted a recently described Agrobacterium-mediated transient expression system. A recombinant single-chain Fv antibody (scFvT84.66) and a full-size mouse/human chimeric antibody (cT84.66) derived from the parental murine mAb T84.66 specific for the human carcinoembryonic antigen were engineered into a plant expression vector. Chimeric T84.66 heavy and light chain genes were constructed by exchanging the mouse light and heavy chain constant domain sequences with their human counterparts and cloned into two independent plant expression vectors. In vivo assembly of full-size cT84.66 was achieved by simultaneous expression of the light and heavy chains after vacuum infiltration of tobacco leaves with two populations of recombinant Agrobacterium. Upscaling the transient system permitted purification of functional recombinant antibodies from tobacco leaf extracts within a week. His6-tagged scFvT84.66 was purified by immobilized metal affinity chromatography and cT84.66 by protein A affinity chromatography. Sufficient amounts of recombinant antibodies were recovered for detailed characterization by SDS/PAGE, Western blotting, and ELISA.
机译:为了评估植物中不同形式的肿瘤特异性抗体的表达,我们采用了最近描述的农杆菌介导的瞬时表达系统。将重组人单链Fv抗体(scFvT84.66)和衍生自对人癌胚抗原具有特异性的亲本鼠mAb T84.66的全尺寸小鼠/人嵌合抗体(cT84.66)工程化为植物表达载体。嵌合的T84.66重链和轻链基因是通过将小鼠轻链和重链恒定域序列与其人类对应物交换而构建的,并克隆到两个独立的植物表达载体中。通过在烟草叶与两个重组农杆菌种群进行真空浸润后同时表达轻链和重链,可以实现全尺寸cT84.66的体内组装。过渡系统的升级允许在一周内从烟叶提取物中纯化功能重组抗体。通过固定的金属亲和色谱纯化带有His6标签的scFvT84.66,通过蛋白A亲和色谱纯化cT84.66。回收了足够数量的重组抗体,以通过SDS / PAGE,Western印迹和ELISA进行详细表征。

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