[Construction and identification of nanobody phage display library targeting Middle East respiratory syndrome coronavirus].

噬菌体展示 抗体 病毒学 重组DNA 肽库 生物 分子生物学 冠状病毒 外周血单个核细胞 中东呼吸综合征冠状病毒 基因 2019年冠状病毒病(COVID-19) 免疫学 医学 肽序列 遗传学 体外 传染病(医学专业) 病理 疾病
作者
Lihua He,Jiangfan Li,Shuo Ren,Shihui Sun,Yan Guo,Hongjie Qiu,Yuanxiang Liao,Kaiyuan Ji,Ruiwen Fan,Guangyu Zhao,Yusen Zhou
出处
期刊:PubMed 卷期号:33 (12): 1662-1668 被引量:3
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Objective To construct a phage display library of specific nano-antibodies against the Middle East respiratory syndrome coronavirus (MERS-CoV) and apply it to the screening of neutralizing nano-antibodies. Methods MERS-CoV receptor-binding domain (RBD) recombinant protein was used to immunize alpaca. After the last immunization, peripheral blood mononuclear cells (PBMCs) were isolated from the whole blood and total RNA was extracted. The VHH gene was amplified by PCR and used to construct recombinant phages. TG1 Escherichia coli was transformed by these recombinant phages. A phage display library of specific nano-antibodies against the MERS-CoV were obtained and used to screen and characterize the nano-antibodies. Results The volume of this library of nano-antibodies was 1.31×108 and its abundance rate was 5.65×1010/mL. The ratio of VHH insertion in the constructed library reached 96%. There was a rich diversity of nano-antibodies in this library. Nano-antibodies with neutralizing activity were identified and expressed from this library. Conclusion We successfully constructed a library of phages which could be effectively applied to the screening of nano-antibodies against MERS-CoV virus.

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