Razanskiene Ausra, Schmidt Jonas, Geldmacher Astrid, Ritzi Andreas, Niedrig Matthias, Lundkvist Ake, Krüger Detlev H, Meisel Helga, Sasnauskas Kestutis, Ulrich Rainer
Institute of Biotechnology, V. Graiciuno 8, LT-2028 Vilnius, Lithuania.
J Biotechnol. 2004 Aug 5;111(3):319-33. doi: 10.1016/j.jbiotec.2004.04.010.
Recently, the high-level expression of authentic and hexahistidine (His)-tagged Puumala (strain Vranica/Hällnäs) hantavirus nucleocapsid protein derivatives in the yeast Saccharomyces cerevisiae has been reported [Dargeviciute et al., Vaccine, 20 (2002) 3523-3531]. Here we describe the expression of His-tagged nucleocapsid proteins of other Puumala virus strains (Sotkamo, Kazan) as well as Dobrava (strains Slovenia and Slovakia) and Hantaan (strain Fojnica) hantaviruses using the same system. All nucleocapsid proteins were expressed in the yeast S. cerevisiae at high levels. The nucleocapsid proteins can be easily purified by nickel chelate chromatography; the yield for all nucleocapsid proteins ranged from 0.5 to 1.5 mg per g wet weight of yeast cells. In general, long-term storage of all nucleocapsid proteins without degradation can be obtained by storage in PBS at -20 degrees C or lyophilization. The nucleocapsid protein of Puumala virus (strain Vranica/Hällnäs) was demonstrated to contain only traces of less than 10 pg nucleic acid contamination per 100 microg of protein. The yeast-expressed nucleocapsid proteins of Hantaan, Puumala and Dobrava viruses described here represent useful tools for serological hantavirus diagnostics and for vaccine development.
最近,已有报道称普马拉(弗拉尼察/哈尔纳斯毒株)汉坦病毒核衣壳蛋白衍生物的天然型和六聚组氨酸(His)标签型在酿酒酵母中实现了高水平表达[达盖维丘特等人,《疫苗》,20(2002)3523 - 3531]。在此,我们描述了使用同一系统表达其他普马拉病毒株(索特卡莫、喀山)以及多布拉瓦(斯洛文尼亚和斯洛伐克毒株)和汉坦(福伊尼察毒株)汉坦病毒的His标签型核衣壳蛋白。所有核衣壳蛋白均在酿酒酵母中高水平表达。核衣壳蛋白可通过镍螯合层析轻松纯化;所有核衣壳蛋白的产量为每克湿重酵母细胞0.5至1.5毫克。一般来说,通过在-20℃的磷酸盐缓冲盐溶液(PBS)中储存或冻干,所有核衣壳蛋白都能长期保存而不降解。已证明普马拉病毒(弗拉尼察/哈尔纳斯毒株)的核衣壳蛋白每100微克蛋白中仅含有痕量低于10皮克的核酸污染物。本文所述的汉坦、普马拉和多布拉瓦病毒的酵母表达核衣壳蛋白是汉坦病毒血清学诊断和疫苗开发的有用工具。