McCormick Christopher J, Maucourant Sophie, Griffin Stephen, Rowlands David J, Harris Mark
Institute of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, UK.
J Gen Virol. 2006 Mar;87(Pt 3):635-640. doi: 10.1099/vir.0.81553-0.
Knowledge of how hepatitis C virus (HCV) proteins associate with components of the host cell to form a functional replication complex is still limited. To address this issue, HCV replicon constructs were generated where either green fluorescent protein (GFP) or the Propionibacterium shermanii transcarboxylase domain (PSTCD) was introduced into the NS5A coding region. Insertion of both GFP and PSTCD was tolerated well, allowing formation of stable replicon-containing cell lines that contained viral protein and transcript levels that were comparable to those of an unmodified parental replicon. Cell lines generated from the GFP-tagged NS5A replicon allowed live-cell visualization of the location of NS5A. Cell lines generated from the PSTCD-tagged replicons allowed rapid and efficient precipitation of the PSTCD-tagged NS5A, as well as other HCV non-structural proteins, using streptavidin-coated magnetic beads. Both replicons represent useful tools that offer different but complementary ways of examining replication-complex formation in cells.
丙型肝炎病毒(HCV)蛋白如何与宿主细胞成分相互作用以形成功能性复制复合体的相关知识仍然有限。为了解决这个问题,构建了HCV复制子,其中绿色荧光蛋白(GFP)或谢氏丙酸杆菌转羧酶结构域(PSTCD)被引入NS5A编码区。GFP和PSTCD的插入均能被良好耐受,从而形成了稳定的含复制子细胞系,这些细胞系中的病毒蛋白和转录水平与未修饰的亲本复制子相当。由GFP标记的NS5A复制子产生的细胞系能够对NS5A的位置进行活细胞可视化观察。由PSTCD标记的复制子产生的细胞系能够使用链霉亲和素包被的磁珠快速有效地沉淀PSTCD标记的NS5A以及其他HCV非结构蛋白。这两种复制子都是有用的工具,它们提供了不同但互补的方法来研究细胞中的复制复合体形成。