Objective To construct expression vector and expression in E.coli of SARS virus E2 protein.
Methods the E2 gene was inserted into pBV220 vector, the recombinant vector of E2 was identificated by restriction endouclease digestion and PCR.E2 protein was expressed in E.coli via induction in 42℃.
Results the analysis for recombinant vector digested by EcoR I and Pst I and PCR demonstrated that the E2 gene was inserted into pBV220.SDS-PAGE showed that the relative molecular mass(Mr)of the expressed E2 protein was about 16600.
Conclusion Expression vector of E2 protein was constructed successfully and expressed effectively in E.coli.these results provided an essential preparation for obtaining a larger quantity of recombinant E2 protein for further study.