Couple production of human calcitonin and rat peptidylglycine alpha-amidation monooxygenase in insect cells.
- Author:
Guan-Zhen YANG
1
;
Zhen-Zhen CHEN
;
Da-Fu CUI
;
Bo-Liang LI
;
Xiang-Fu WU
Author Information
1. Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Baculoviridae;
genetics;
Calcitonin;
biosynthesis;
genetics;
Cells, Cultured;
Gene Expression;
Glutathione Transferase;
genetics;
Humans;
Insecta;
cytology;
Mixed Function Oxygenases;
biosynthesis;
genetics;
Multienzyme Complexes;
biosynthesis;
genetics;
Rats;
Recombinant Fusion Proteins;
genetics
- From:
Chinese Journal of Biotechnology
2002;18(1):20-24
- CountryChina
- Language:Chinese
-
Abstract:
Human calcitonin (hCT) is a 32 amino acid peptide hormone that requires C-terminal amidation for full biological activity. Calcitonin has important physiological function in vivo. We describe the couple expression of a synthesized modified human calcitonin(hmCT) gene fused with glutathione-S-transferase and rat peptidylglycine alpha-amidation monooxygenase (PAM) in insect cells infected by recombinant baculovirus GSTCT/PAM. Using Western blotting against hmCT or rat PAM, the GSThmCT fusion protein had been identified as well as the PAM. Following affinity chromatography with glutathione agarose column, the GSThmCT fusion protein produced by insect cells was purified. The purified fusion protein was also interacted with antibody against hmCT. The couple expression of a modification enzyme and its substrate in eucaryotic expression system may be used for producing other biological activity peptides.
