Maksimova T G, Bakhvalova V N, Morozova O V
Vopr Virusol. 1998 Jan-Feb;43(1):36-9.
Affinity chromatography of lysates of continuous porcine embryo cells infected with tick-borne encephalitis (TBE) virus on sepharose with immobilized monoclonal antibodies to TBE virus proteins NS5 and NS3 results in isolation of a stable protein complex. This complex contains viral proteins NS5, NS3, p49, and, probably, two more cell proteins. This complex is not detected at the early stage of infection, and 24 h after infection its structure does not depend on the specificity of immobilized monoclonal antibodies used in affinity chromatography and on the time elapsed after the infection. Immunoprecipitates of infected cells phosphorylated TBE virus protein NS5 in vitro, but possessed no RNA-polymerase activity. Elution of the complex with buffers with pH 3.5 or 11.1 or with 2M urea failed to purify the active replicase. The complex of viral and cellular proteins isolated by affinity chromatography on different immunoadsorbents did not possess RNA-polymerase activity because of inactivation or absence of additional subunit(s).
用固定有抗蜱传脑炎(TBE)病毒蛋白NS5和NS3单克隆抗体的琼脂糖对感染TBE病毒的猪胚胎连续细胞裂解物进行亲和层析,可分离出一种稳定的蛋白质复合物。该复合物包含病毒蛋白NS5、NS3、p49,可能还包含另外两种细胞蛋白。在感染早期未检测到这种复合物,感染后24小时,其结构不依赖于亲和层析中使用的固定化单克隆抗体的特异性以及感染后经过的时间。感染细胞的免疫沉淀物在体外使TBE病毒蛋白NS5磷酸化,但不具有RNA聚合酶活性。用pH 3.5或11.1的缓冲液或2M尿素洗脱该复合物未能纯化出活性复制酶。通过在不同免疫吸附剂上进行亲和层析分离得到的病毒和细胞蛋白复合物由于失活或缺少其他亚基而不具有RNA聚合酶活性。