Selection by phage display of nanobodies directed against hypoxia inducible factor-1α (HIF-1α)

被引:8
|
作者
Li, Min [1 ,2 ,3 ]
Fan, Xiaodan [1 ,2 ,3 ]
Liu, Jing [1 ,2 ,3 ]
Hu, Yaozhong [1 ,2 ,3 ]
Huang, He [1 ,2 ,3 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Dept Biochem Engn, Tianjin 300072, Peoples R China
[2] Tianjin Univ, Minist Educ, Key Lab Syst Bioengn, Tianjin 300072, Peoples R China
[3] Collaborat Innovat Ctr Chem Sci & Engn, Tianjin, Peoples R China
关键词
anti-HIF-1; alpha; PAS-B; nanobodies; ELISA; phage display technology; DOMAIN ANTIBODY FRAGMENTS; OXYGEN HOMEOSTASIS; SINGLE; HIF-1; EXPRESSION; CYTOPLASM; TUMORS;
D O I
10.1002/bab.1340
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hypoxia, which promotes tumor invasion and metastasis, is a common phenomenon in solid tumors. Hypoxia generally leads to a higher expression level of hypoxia inducible factor-1 (HIF-1) in tumors (cells) relative to normal tissues (cells). Given the unique expression of HIF-1 in human cancers and its vital importance in mediating hypoxic adaptation, we have identified 20 different HIF-1-specific nanobodies by using a llama-derived nonimmune phage display library. PAS-B domain of HIF-1 (HIF-1-PAS-B) has been used as an antigen. Nanobody (VHH16) was selected from these 20 nanobodies by phage enzyme-linked immunosorbent assay. The preliminary analysis of biological activity demonstrates that VHH16 can specifically bind to HIF-1 with high affinity. VHH16 is the first nanobody that specifically binds to HIF-1-PAS-B as well. We suggest here that VHH16 is useful in disease diagnosis and also has potential in medical applications. (C) 2014 International Union of Biochemistry and Molecular Biology, Inc.
引用
收藏
页码:738 / 745
页数:8
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