Prokaryotic expression and pilot application of capsid proteins of WU polyomavirus
Antigenicity
DOI:
10.3760/cma.j.issn.0254-5101.2011.06.013
Publication Date:
2011-06-30
AUTHORS (6)
ABSTRACT
Objective To express the capsid proteins of WU polyomavirus(WUPyV) for research and find antigen diagnostic value. Methods Coding sequences polyomavirus by PCR were cloned in prokaryotic expression vector PGEX-20T. Recombinant plasmids transformed into E. coli BL21(DE3) induced IPTG expression. identified Western blot. Results SDS-PAGE proved that recombinant showed three bands with molecular relative mass 69×103, 63×103 56×103. The recognized anti-GST McAb. antigenicity was tested blot using 16 positive 70 negative sera. Conclusion VP1, VP2 VP3 expressed can combine WUPyV-Ab have good antigenicity. They be used further research.
Key words:
WU polyomavirus; Capsid protein; Prokaryotic
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