Lukashevich I S, Lemeshko N N, Golubev V P
Vopr Virusol. 1985 Jul-Aug;30(4):457-63.
Machupo virus labeled with radioactive precursors of RNA or protein synthesis was purified by isodensity ultracentrifugation in sucrose concentration gradient. The purified virus was disrupted with NP-40 nonionic detergent in the presence of 1 M KCl, and subvirion fractions were separated by ultracentrifugation in urografin density gradient. This treatment resulted in formation of two subvirion components with a buoyant density 1.25-1.26 and 1.10-1.12 g/cm3 in urografin concentration gradient. The subvirion fraction with the density of 1.25-1.26 g/cm3 contained high-molecular virion RNAs, a major protein of molecular weight of 64 kD, and seemed to be the virion nucleocapsid. The solubilised fraction (1.10-1.12 g/cm3) contained glycosylated protein 37 kD which seems to be a surface glycoprotein.
用RNA或蛋白质合成的放射性前体标记的马丘波病毒,通过在蔗糖浓度梯度中进行等密度超速离心进行纯化。纯化后的病毒在1M氯化钾存在的情况下用NP - 40非离子去污剂裂解,亚病毒粒子组分通过在泛影葡胺密度梯度中进行超速离心分离。这种处理在泛影葡胺浓度梯度中形成了两个亚病毒粒子组分,其浮力密度分别为1.25 - 1.26和1.10 - 1.12 g/cm³。密度为1.25 - 1.26 g/cm³的亚病毒粒子组分含有高分子量的病毒粒子RNA、一种分子量为64 kD的主要蛋白质,似乎是病毒粒子核衣壳。溶解组分(1.10 - 1.12 g/cm³)含有糖基化的37 kD蛋白质,似乎是一种表面糖蛋白。