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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.
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页码:738 / 745
页数:8
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