Department of Microbiology, Faculty of Biotechnology and Biomolecular Sciences, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia.
J Virol Methods. 2011 Jul;175(1):74-9. doi: 10.1016/j.jviromet.2011.04.021. Epub 2011 Apr 28.
Macrobrachium rosenbergii nodavirus (MrNv) infects giant freshwater prawns and causes white tail disease (WTD). The coding region of the capsid protein of MrNv was amplified with RT-PCR and cloned into the pTrcHis2-TOPO vector. The recombinant plasmid was introduced into Escherichia coli and protein expression was induced with IPTG. SDS-PAGE showed that the recombinant protein containing the His-tag and myc epitope has a molecular mass of about 46 kDa and it was detected by the anti-His antibody in Western blotting. The protein was purified using immobilized metal affinity chromatography (IMAC) and transmission electron microscopic analysis revealed that the recombinant protein assembled into virus-like particles (VLPs) with a diameter of about 30±3 nm. The size of the particles was confirmed by dynamic light scattering. Nucleic acids were extracted from the VLPs and treatment with nucleases showed that they were mainly RNA molecules. This is the first report describing the production of MrNv capsid protein in bacteria and its assembly into VLPs.
罗氏沼虾诺达病毒(MrNv)感染巨型淡水虾并引起白尾病(WTD)。使用 RT-PCR 扩增 MrNv 衣壳蛋白的编码区,并将其克隆到 pTrcHis2-TOPO 载体中。将重组质粒导入大肠杆菌,并使用 IPTG 诱导蛋白表达。SDS-PAGE 显示,含有 His 标签和 myc 表位的重组蛋白的分子量约为 46 kDa,并在 Western blot 中被抗 His 抗体检测到。使用固定化金属亲和层析(IMAC)纯化蛋白,透射电子显微镜分析显示重组蛋白组装成直径约 30±3nm 的病毒样颗粒(VLPs)。通过动态光散射确认颗粒的大小。从 VLPs 中提取核酸,用核酸酶处理表明它们主要是 RNA 分子。这是首次描述在细菌中生产 MrNv 衣壳蛋白及其组装成 VLPs。