Welling G W, Groen G, Slopsema K, Welling-Wester S
J Chromatogr. 1985 Jun 19;326:173-8. doi: 10.1016/s0021-9673(01)87443-4.
Virus envelope proteins obtained by Triton X-100 extraction of Sendai virions were purified to a high degree by a combination of high-performance liquid chromatography (HPLC) methods. Size-exclusion HPLC on a TSK 4000 PW column with several concentrations of acetonitrile or ethanol-1-butanol in 0.1% hydrochloric acid as eluent was used as the first chromatographic step. Peak fractions were diluted in water and further fractionated on reversed-phase columns (TMS-250 or Vydac 218 TP). Size-exclusion HPLC with 45% acetonitrile in 0.1% hydrochloric acid, combined with reversed-phase HPLC on either column, was most suitable for obtaining highly purified F2 protein. Antibodies obtained after injection of this protein were reactive with the intact virus.
通过用Triton X-100提取仙台病毒粒子获得的病毒包膜蛋白,采用高效液相色谱(HPLC)方法组合进行了高度纯化。第一步色谱分离采用在TSK 4000 PW柱上进行尺寸排阻HPLC,以0.1%盐酸中几种浓度的乙腈或乙醇-1-丁醇作为洗脱剂。将峰级分用水稀释,然后在反相柱(TMS-250或Vydac 218 TP)上进一步分离。在0.1%盐酸中含45%乙腈的尺寸排阻HPLC,与任一柱上的反相HPLC相结合,最适合于获得高度纯化的F2蛋白。注射该蛋白后获得的抗体与完整病毒具有反应性。