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首页> 外文期刊>Frontiers in bioscience: a journal and virtual library >Use of hr3 enhancer and P74 TM domain in baculovirus surface display
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Use of hr3 enhancer and P74 TM domain in baculovirus surface display

机译:hr3增强子和P74 TM域在杆状病毒表面展示中的用途

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摘要

Baculovirus surface display technique provides a new platform for novel vaccine research and production. Unfortunately, the low display efficiency in current methods and the waste of occlusion-derived virion (ODV) products limited its application. We investigated the use of two motifs, BmNPV hr3 and transmembrane domain of P74 (P74TM), in display. Budding virus (BV) with hr3 showed a 14.2-time enhanced display efficiency than the current recombinant BV. Hemagglutinin (HA) protein of H5N1 influenza virus was displayed by using 3 different vectors to ensure the improvement of display efficiency and the characters of displayed protein in recombinant baculovirus. Immunoassay demonstrated that the recombinant BV with TM/CTD of vsvG protein, and hr3 could induce the highest level of neutralizing antibody against HA, suggesting that the optimized HA displaying BV could be a novel live virus-based vaccine candidate for influenza virus. In addition, GFP fused with the P74TM could be anchored to the ring zone in infected cell and the ODV envelope, which may luminate a new direction for ODV display and provide a promising strategy to use ODV products.
机译:杆状病毒表面展示技术为新型疫苗的研究和生产提供了新的平台。不幸的是,当前方法的低显示效率和源自遮挡的病毒体(ODV)产品的浪费限制了其应用。我们研究了两个母题BmNPV hr3和P74跨膜结构域(P74TM)的使用。与目前的重组BV相比,带有hr3的萌芽病毒(BV)显示显示效率提高了14.2倍。通过使用3种不同的载体展示H5N1流感病毒的血凝素(HA)蛋白,以确保提高重组杆状病毒的展示效率和展示蛋白的特性。免疫分析表明,带有vsvG蛋白的TM / CTD的重组BV和hr3可以诱导最高水平的针对HA的中和抗体,这表明优化的展示HA的HA可能是新型的基于活病毒的流感病毒候选疫苗。此外,与P74TM融合的GFP可以锚定在感染细胞和ODV包膜的环带上,这可能为ODV展示提供新的方向,并为使用ODV产品提供了有希望的策略。

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