表位
抗体
干瘪的
计算生物学
抗原
Wnt信号通路
生物
细胞生物学
免疫学
信号转导
作者
Qiangqiang Ge,Maikun Teng,Xu Li,Qiong Guo,Yuyong Tao
出处
期刊:Structure
[Elsevier]
日期:2023-01-01
卷期号:31 (1): 33-43.e5
被引量:5
标识
DOI:10.1016/j.str.2022.11.009
摘要
The lack of incorporating epitope information into the selection process makes the conventional antibody screening method less effective in identifying antibodies with desired functions. Here, we developed an epitope-directed antibody selection method by designing a directed library favoring the target epitope and a precise "counter" antigen for clearing irrelevant binders in the library. With this method, we successfully isolated an antibody, pF7_A5, that targets the less conserved region on the FZD2/7 CRD as designed. Guided by the structure of pF7_A5-FZD2CRD, a further round of evolution was conducted together with the "counter" antigen selection strategy, and ultimately, an FZD2-specific antibody and an FZD7-preferred antibody were obtained. Because of targeting the predefined functional site, all these antibodies exhibited the expected modulatory activity on the Wnt pathway. Together, the method developed here will be useful in antibody drug discovery, and the identified FZD antibodies will have clinical potential in FZD-related cancer therapy.
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