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Production of the HBc Protein from Different HBV Genotypes in E. coli. Use of Reassociated HBc VLPs for Packaging of ss- and dsRNA

机译:从大肠杆菌中产生来自不同HBV基因型的HBC蛋白。使用REARSOCIED HBC VLP进行SS-和DSRNA的包装

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摘要

The core proteins (HBc) of the hepatitis B virus (HBV) genotypes A, B, C, D, E, F, and G were cloned and expressed in Escherichia coli (E. coli), and HBc-formed virus-like particles (VLPs) were purified with ammonium sulfate precipitation, gel filtration, and ion exchange chromatography (IEX). The best VLP yield was found for the HBc of the HBV genotypes D and G. For the HBc of the HBV genotypes D, F, and G, the possibility of dissociation and reassociation maintaining the native HBc structure was demonstrated. Single-stranded (ss) and double-stranded (ds) ribonucleic acid (RNA) was successfully packed into HBc VLPs for the HBV genotypes D and G.
机译:丙型肝炎病毒(HBV)基因型A,B,C,D,E,F和G的核心蛋白(HBC)被克隆并在大肠杆菌(大肠杆菌)中表达,以及HBC形成的病毒样颗粒(VLP)用硫酸铵沉淀,凝胶过滤和离子交换色谱(Iex)纯化。对于HBV基因型D和G.对于HBV基因型D,F和G的HBC,发现了最佳的VLP产量D和G,证明了保持天然HBC结构的解离和重新分配的可能性。单链(SS)和双链(DS)核糖核酸(RNA)成功填充到HBC VLP中,用于HBV基因型D和G.

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