HAN Gang, GAO Jiangping, YAN Jinqi, JIA Rui, ZHANG Liang, DONG Jinkai, TIAN Renli, WANG Xiaoxiong, YU Jiyun. Construction and eukaryotic expression of DNA vaccine encoding heterological prostate stem cell antigen for prostate cancerJ. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2009, 30(1): 88-90.
Citation: HAN Gang, GAO Jiangping, YAN Jinqi, JIA Rui, ZHANG Liang, DONG Jinkai, TIAN Renli, WANG Xiaoxiong, YU Jiyun. Construction and eukaryotic expression of DNA vaccine encoding heterological prostate stem cell antigen for prostate cancerJ. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2009, 30(1): 88-90.

Construction and eukaryotic expression of DNA vaccine encoding heterological prostate stem cell antigen for prostate cancer

  • Objective: To construct a DNA vaccine containing heterological genetic sequence encoding most cytotoxic lymphocyte epitopes of human prostate stem cell antigen(PSCA)——pVAX1-PSCA3-Fc-GPI-IRES-GM/B7(pVAX1-PSCA3FcGB),and detect its expression in a eukaryotic cell Cos7. Methods: The heterological PSCA genetic fragment was synthesized by overlapping extending-PCR,and then 3 copies of the fragment(PSCA3) were linked up by co-adhesive end restriction and ligation strategy.The PSCA3 fragment was inserted into a eukaryotic expression vector pCI-Fc-GPI including the gene of the signal peptide of human Igк,human IgG-Fc and glycosyl phosphatidyl inositol(GPI).At last,the fusion genetic fragment PSCA3-Fc-GPI was cloned into the final eukaryotic expression vector-pVAX1-IRES-GM/B7 which includes several genetic fragments encoding internal ribozyme entry site(IRES),human granulocyte-macrophage colony-stimulating factor(GM-CSF) and costimulatory molecules-B7.1 at the downstream of the inserted site.The final recombinant plasmid pVAX1-PSCA3FcGB DNA vaccine was liposomally transfected into Cos7 cells.And the expression of this DNA vaccine was detected by immunofluorescence and flow cytometry. Results: DNA sequencing result confirmed that the sequence of heterological PSCA genetic fragment was consistent with the design.Enzyme digestion analysis showed that the recombinant plasmid-pVAX1-PSCA3FcGB DNA vaccine was successfully constructed.The expression of the DNA vaccine in eukaryotic cells was demonstrated by immunofluorescence and flow cytometry. Conclusion: The DNA vaccine-pVAX1-PSCA3FcGB has been successfully constructed and well expressed in Cos7 cells.These results have provided necessary bases for the study of the anti-prostate cancer effect of this vaccine in the future.
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