Rombaut B, Foriers A, Boeyé A
Department of Microbiology and Hygiene, Vrije Universiteit Brussel, Belgium.
J Virol Methods. 1990 Sep;29(3):303-11. doi: 10.1016/0166-0934(90)90057-m.
Purification of 14 S subunits from extracts of poliovirus-infected HeLa cells was achieved by a combination of sucrose gradient ultracentrifugation and high-performance size-exclusion chromatography. The particles were free of admixtures of other subviral particles, of nonstructural viral proteins, and of host cell proteins. The purified material retained the physical and antigenic properties of native 14 S subunits fully, as well as their ability to assemble to empty capsids in vitro.
通过蔗糖梯度超速离心和高效尺寸排阻色谱相结合的方法,从感染脊髓灰质炎病毒的HeLa细胞提取物中纯化出了14S亚基。这些颗粒不含其他亚病毒颗粒、非结构病毒蛋白和宿主细胞蛋白的混合物。纯化后的物质完全保留了天然14S亚基的物理和抗原特性,以及它们在体外组装成空衣壳的能力。