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Assembly of tomato blistering mosaic virus-like particles using a baculovirus expression vector system

机译:使用杆状病毒表达载体系统组装番茄洗起马马赛克病毒样颗粒

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The expression of several structural proteins from a wide variety of viruses in heterologous cell culture systems results in the formation of virus-like particles (VLPs). These VLPs structurally resemble the wild-type virus particles and have been used to study viral assembly process and as antigens for diagnosis and/or vaccine development. Tomato blistering mosaic virus (ToBMV) is a tymovirus that has a 6.3-kb positive-sense ssRNA genome. We have employed the baculovirus expression vector system (BEVS) for the production of tymovirus-like particles (tVLPs) in insect cells. Two recombinant baculoviruses containing the ToBMV wild-type coat protein (CP) gene or a modified short amino-terminal deletion (2-24CP) variant were constructed and used to infect insect cells. Both recombinant viruses were able to express ToBMV CP and 2-24CP from infected insect cells that self-assembled into tVLPs. Therefore, the N-terminal residues (2-24) of the native ToBMV CP were shown not to be essential for self-assembly of tVLPs. We also constructed a third recombinant baculovirus containing a small sequence coding for the major epitope of the chikungunya virus (CHIKV) envelope protein 2 (E2) replacing the native CP N-terminal 2-24 amino acids. This recombinant virus also produced tVLPs. In summary, ToBMV VLPs can be produced in a baculovirus/insect cell heterologous expression system, and the N-terminal residues 2-24 of the CP are not essential for this assembly, allowing its potential use as a protein carrier that facilitates antigen purification and might be used for diagnosis.
机译:在异源细胞培养系统中,来自各种病毒的若干结构蛋白的表达导致含有病毒样颗粒(VLP)的形成。这些VLP在结构上类似于野生型病毒颗粒,并且已用于研究病毒组装过程和作为抗原用于诊断和/或疫苗发育。番茄起泡的马赛克病毒(ToBMV)是一种Tymovirus,具有6.3kb的阳性感测SsRNA基因组。我们使用杆状病毒表达载体系统(BEV)用于在昆虫细胞中生产Tymovirus样颗粒(TVLPS)。构建含有ToBMV野生型涂层蛋白(CP)基因或改性的短氨基末端缺失(2-24CP)变体的两种重组杆状病毒,并用于感染昆虫细胞。两种重组病毒都能够从被自组装到TVLPS的感染昆虫细胞中表达ToBMV CP和2-24CP。因此,显示天然ToBMV CP的N-末端残基(2-24)对于TVLP的自组装,不是必不可少的。我们还构建了一种第三次重组杆状病毒,其含有小序列编码,用于替代天然Cp N-末端2-24氨基酸的Chikungunya病毒(Chikv)包络蛋白2(E2)的主要表位。该重组病毒还生产TVLPS。总之,可以在杆状病毒/昆虫细胞异源表达系统中产生TOBMV VLP,并且CP的N-末端残基2-24对于该组件不是必需的,允许其潜在用作促进抗原纯化的蛋白质载体可能用于诊断。

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