首页> 外文期刊>Journal of Virological Methods >Recombinant haemagglutinin protein of highly pathogenic avian influenza A (H5N1) virus expressed in Pichia pastoris elicits a neutralizing antibody response in mice.
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Recombinant haemagglutinin protein of highly pathogenic avian influenza A (H5N1) virus expressed in Pichia pastoris elicits a neutralizing antibody response in mice.

机译:在巴斯德毕赤酵母中表达的高致病性禽流感A(H5N1)病毒重组血凝素蛋白引起小鼠中和抗体反应。

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摘要

Recombinant avian influenza vaccines offer several advantages over the conventional vaccines. In this study, the haemagglutinin (HA) gene of highly pathogenic avian influenza H5N1 was cloned and expressed as His tagged protein in methylotropic yeast Pichia pastoris. The expression of recombinant HA (rHA) protein was confirmed by SDS-PAGE and western blot analysis. The rHA protein was purified using Ni-NTA affinity chromatography under denaturing conditions and the functions of the protein was assessed by the haemagglutinin assay after refolding. The immunogenicity of the rHA was evaluated by immunizing four groups of mice with different payloads (2.5, 5.0, 10 and 25 micro g) of purified rHA and the production of rHA specific antibodies were analysed by haemagglutinin inhibition assay (HI) and enzyme-linked immunosorbent assay (ELISA). An antigen specific immune response was observed against rHA indicating that the rHA antigen could be used as a vaccine candidate against avian influenza. These results suggest that this strategy would pave the way for the development of rapid and cost effective method for the production of an avian influenza vaccine.
机译:重组禽流感疫苗比常规疫苗具有多个优势。在这项研究中,高致病性禽流感H5N1的血凝素(HA)基因被克隆并表达为His标记蛋白,在多甲基酵母Pichia pastoris中。通过SDS-PAGE和蛋白质印迹分析证实了重组HA(rHA)蛋白的表达。在变性条件下,使用Ni-NTA亲和色谱纯化rHA蛋白,并在重折叠后通过血凝素测定评估该蛋白的功能。通过用不同有效载荷(2.5、5.0、10和25微克)纯化的rHA免疫四组小鼠来评估rHA的免疫原性,并通过血凝素抑制试验(HI)和酶联法分析rHA特异性抗体的产生免疫吸附测定(ELISA)。观察到针对rHA的抗原特异性免疫应答,表明rHA抗原可用作抗禽流感的候选疫苗。这些结果表明,该策略将为开发快速且经济高效的禽流感疫苗生产方法铺平道路。

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