双特异性抗体
抗体
化学
免疫球蛋白Fab片段
表位
细胞毒性
重组DNA
分子生物学
CD16
免疫系统
计算生物学
单克隆抗体
生物
免疫学
生物化学
互补决定区
CD3型
体外
CD8型
基因
作者
Yanlan Wang,Jiayu Liu,Haitao Pan,Jieyu Xing,Xiaoqiong Wu,Qing Li,Zhong Wang
摘要
This protocol describes the construction and functional studies of a bispecific antibody (bsAb), GPC3-S-Fab. bsAbs can recognize two different epitopes through their two different arms. bsAbs have been actively studied for their ability to directly recruit immune cells to kill tumor cells. Currently, the majority of bsAbs are produced in the form of recombinant proteins, either as Fc-containing bsAbs or as smaller bsAb derivatives without the Fc region. In this study, GPC3-S-Fab, an antibody fragment (Fab) based bispecific antibody, was designed by linking the Fab of anti-GPC3 antibody GC33 with an anti-CD16 single domain antibody. The GPC3-S-Fab can be expressed in Escherichia coli and purified by two affinity chromatographies. The purified GPC3-S-Fab can specifically bind to and kill GPC3 positive liver cancer cells by recruiting natural killer cells, suggesting a potential application of GPC3-S-Fab in liver cancer therapy.
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