The cloning expression, purification and activity of human angiostatin K (1-3) gene.
- Author:
Yun-Long WANG
1
;
Guo-Qiang WANG
;
Zhi-Tao LI
;
Xiao-Ya LU
;
Yu-Lin LI
;
Zhen WANG
Author Information
- Publication Type:Journal Article
- MeSH: Angiostatins; genetics; isolation & purification; metabolism; Cloning, Molecular; Escherichia coli; genetics; metabolism; Gene Expression; Humans; Liver; metabolism; Recombinant Fusion Proteins; genetics; isolation & purification; metabolism
- From: Chinese Journal of Experimental and Clinical Virology 2009;23(3):191-193
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo clone the sequence of human Angiostatin cDNA and obtain the protein of recombinant angiostatin for further development.
METHODSFresh human liver tissue was used for the extraction of total RNA and amplified the Angiostatin cDNA through RT-PCR method . After the recombinant plasmid pET30a-Angiostatin was constructed and confirmed, it was transduced into Rosetta (DE3). Then the transformation was used for fermentation and induced expression. The protein was identified by Western Blot and purified by Ni-NTA affinity chromatography.
RESULTSThe sequence of human Angiostatin cDNA was identical with genebank. Angiostatin (K1-3) was expressed and purified. The target protein made up 30% of the total bacterial protein. The purity is above 90%.
CONCLUSIONAngiostatin K (1-3) can be reached using fusion vector pET30a. The product have the biological activity.
