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Journal of Southern Medical University ; (12): 1846-1850, 2011.
Article in Chinese | WPRIM | ID: wpr-333799

ABSTRACT

<p><b>OBJECTIVE</b>To clone the genes encoding the structural proteins VP1-VP4 of enterovirus 71 and investigate the immunogenicity of the expressed recombinant proteins.</p><p><b>METHODS</b>The VP1-VP4 cDNAs were amplified by RT-PCR from the extracted viral RNA and cloned into pMD19-T vector. The cloned VP1-VP4 genes were then inserted into the multi-cloning sites of plasmid pQE30a and expressed in E. coli M15 with IPTG induction. After washing with 8 mol/L urea and purification with Ni-affinity chromatography, the recombinant proteins obtained were tested for immunogenicity by Western blotting and ELISA using rabbit antisera against enterovirus 71 and Coxsackie Virus A16.</p><p><b>RESULTS</b>The recombinant VP1-VP4 proteins were highly expressed in E. coli M15 and the purified proteins could be specifically recognized by the rabbit sera against enterovirus 71.</p><p><b>CONCLUSION</b>The expressed enterovirus 71 structural proteins show good immunogenicity and can be used for developing enterovirus 71 vaccine and detection kits.</p>


Subject(s)
Animals , Humans , Mice , Rabbits , Capsid Proteins , Genetics , Allergy and Immunology , Cloning, Molecular , Enterovirus A, Human , Genetics , Allergy and Immunology , Enterovirus Infections , Virology , Escherichia coli , Genetics , Metabolism , Immunogenetic Phenomena , Recombinant Proteins , Genetics , Allergy and Immunology
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