Cloning, expression and biological activity identification of a cDNA encoding the extracellular region of human b7-2.
- Author:
Zhi-Hong YUAN
1
;
Yong-Zhi XI
;
Fan-Hua KONG
;
Hui-Li ZHANG
;
Liu NAN
;
Fei LIANG
Author Information
1. Department of Immunology, Hospital Affiliated to Academy of Military Medical Sciences, Laboratory of Immunoassay, National Center of Biomedical Analysis, Beijing 100039, China.
- Publication Type:Journal Article
- MeSH:
Antigens, CD;
biosynthesis;
genetics;
pharmacology;
B7-2 Antigen;
Blotting, Western;
Cloning, Molecular;
DNA, Complementary;
analysis;
Humans;
Membrane Glycoproteins;
biosynthesis;
genetics;
pharmacology;
Recombinant Proteins;
biosynthesis;
isolation & purification;
pharmacology
- From:
Journal of Experimental Hematology
2002;10(6):508-511
- CountryChina
- Language:Chinese
-
Abstract:
As one important member of B7/CD28/CTLA-4 costimulatory signal pathway, B7-2 molecule plays a critical role in regulating T-cell response. In order to further explore its effects on regulation of T cell activation, proliferation and associated signal pathways, the cDNA encoding extracellular region of human B7-2 was amplified via PCR and subcloned into some prokaryotic expression vectors to express target protein in host strains. The expressed protein was identified with Western blot and MTT. Results showed that after screening, the expression level of the protein of interest attained the yield of over 20% total bacterial protein by using pGEX-4T-2 vector and E. coli BL21 (DE3)-CodonPlus-RIL host cells. The recombinant protein could specially react with B7-2 McAb and could stimulate T-cell proliferation combined with anti-CD3 antibody. In conclusion, the recombinant protein was bioactive, therefore the study will make it possible for the research of relationship between B7-2 structure and its function.
