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Chinese Journal of Biotechnology ; (12): 914-918, 2006.
Article in Chinese | WPRIM | ID: wpr-325450

ABSTRACT

To construct and express Hsp70-HSV2gD fusion protein. Genes of Hsp70 and HSV-2gD were subcloned into vectors pGEX-4T-1 respectively. After confirmed by DNA sequence analysis, the recombinant plasmids pGEX-4T-HSP-gD was transformed into E. coli DH5alpha and induced to express with IPTG. The expressed protein was characterized by SDS-PAGE and Western blot after purified. BALB/c mice were immunized with fusion proteins respectively via intra-m uscular injection. The proliferation of spleen lymphocytes, the level of y-IFN in culture and anti-HSV-2gD IgG antibody in serum was detected was detected. The expressed protein was analyzed by SDS-PAGE after induced with IPTG, which showed a new band with an apparent molecular mass corresponding to the predicted size (118 kD). Western Blotting analysis demonstrates that the purified Hsp70-HSV2gD fusion protein had specific binding activity. The stimulation indexes of spleen lymphocytes, the level of gamma-IFN in culture and anti-HSV-2gD IgG antibody in serum of GST-Hsp70-gD group was obviously higher than that of other groups (P < 0.05 respectively). The successful expression of the Hsp70-HSV2gD fusion protein, which can induce immune responses, laid a solid foundation for its further research.


Subject(s)
Animals , Mice , Blotting, Western , Cell Proliferation , Gene Expression , HSP70 Heat-Shock Proteins , Genetics , Allergy and Immunology , Immunoglobulin G , Blood , Allergy and Immunology , Interferon-gamma , Blood , Plasmids , Genetics , Recombinant Fusion Proteins , Genetics , Allergy and Immunology , Spleen , Cell Biology , Allergy and Immunology , Viral Envelope Proteins , Genetics , Allergy and Immunology
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