Soluble expression, purification and characterization of recombinant Tp0136 selective fragment from Treponema pallidum
10.3760/cma.j.issn.0254-5101.2011.02.006
- VernacularTitle:梅毒螺旋体Tp0136活性肽段的可溶性表达、纯化及鉴定
- Author:
Jun YANG
;
Lin SHEN
;
Xiaoxian ZHANG
;
Qi SUN
- Publication Type:Journal Article
- Keywords:
Treponema pallidum;
Tp0136;
Selective fragment;
Soluble expression;
Immunity activity
- From:
Chinese Journal of Microbiology and Immunology
2011;31(2):119-123
- CountryChina
- Language:Chinese
-
Abstract:
Objective To express and purify recombinant Tp0136 epitope fragment, and study the immunity activity. Methods The Tp0136 selective fragment(Tp0136B) gene was devised by the surface property analysis, solvent-accessible suface calculateions, secondary structure function region analysis, and was inserted between the sites of Nde Ⅰ and Not Ⅰ in pET22b ( + ) . The recombinant plasmid was expressed in E. coli BI21. After nickel ion metal affinity chromatography, the antigenic and immune reactivity of rTp0136B was confirmed. Then indirect ELISA with the rTp0136B as coating antigen was performed to detect the anti-Tp0136 antibody in sera from 100 normal human controls and 131 primary syphilis patients. Results The rTp0136B was soluble expressed with a molecular weight of about 28 000 and was obtained with a purity of ＞98% by chromatography. Western blot proved that the rTp0136B could specifically react with anti-Tp0136 polyclonal antibody. Specific humoral response was elicited by the recombinant protein in Japan negative. The positive detection rate in sera from primary syphilis patients was 85.5%. Conclusion This result suggested that the recombinant Tp0136 epitope fragments have a satisfactory immunocompetence,which may have applications in the serodiagnosis of primary syphilis.
