Petrovskis Ivars, Lieknina Ilva, Dislers Andris, Jansons Juris, Bogans Janis, Akopjana Inara, Zakova Jelena, Sominskaya Irina
Latvian Biomedical Research and Study Centre, Ratsupites 1, LV-1067 Riga, Latvia.
Microorganisms. 2021 Jan 30;9(2):283. doi: 10.3390/microorganisms9020283.
The core proteins (HBc) of the hepatitis B virus (HBV) genotypes A, B, C, D, E, F, and G were cloned and expressed in ), 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.
克隆了乙型肝炎病毒(HBV)A、B、C、D、E、F和G基因型的核心蛋白(HBc)并在[具体表达系统未给出]中表达,通过硫酸铵沉淀、凝胶过滤和离子交换色谱(IEX)纯化了由HBc形成的病毒样颗粒(VLP)。发现HBV D和G基因型的HBc产生的VLP产量最高。对于HBV D、F和G基因型的HBc,证明了其解离和重新缔合并维持天然HBc结构的可能性。成功地将单链(ss)和双链(ds)核糖核酸(RNA)包装到HBV D和G基因型的HBc VLP中。