On the basis of successful cloning the full length hemagglulinin (HA) and neuramidinase (NA) gene and sequence analysis of influenza virus H1N1, part of the gene was ligated into pMETA. Expression vectors pMETA/HA (52–1 557 bp) and pMETA/NA (121–1 263 bp) were constructed and expressed in pMAD16 induced by methanol. Recombinant protein was purified through Ni2+ affinity chromatography. Western blotting and ELISA were used to determine the antigenic activity of the recombinant protein. SDS-PAGE showed that the recombinant capsid gene could be overexpressed in Pichia methanolica. ELISA and Western blotting showed that the recombinant protein had antigenicity.
张烨,于在江,辛丽,陈永坤,唐启慧,陈禹保,陈清轩,舒跃龙. 流感病毒H1N1血凝素基因和神经氨酸酶基因在酵母菌中的表达[J]. Chinese Journal of Biotechnology, 2010, 26(8): 1068-1073
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