Winkler G, Randolph V B, Cleaves G R, Ryan T E, Stollar V
Department of Molecular Genetics and Microbiology, Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey, Piscataway 08854.
Virology. 1988 Jan;162(1):187-96. doi: 10.1016/0042-6822(88)90408-4.
Evidence is presented which indicates that the dengue-2 virus nonstructural protein NS1 (soluble complement fixing antigen) exists in infected BHK and mosquito cell cultures as part of a stable oligomer. Identification of the dissociation products of the isolated oligomer and comparison of the number of N-linked glycans in native and denatured NS1 is consistent with the idea that the high-molecular-weight form of NS1 is a homodimer. By analyzing lysates of BHK cells infected with St. Louis encephalitis virus or Powassan virus and proteins from dengue-2 virus-infected mouse brain we have demonstrated that the appearance of the high-molecular-weight form of NS1 is a general feature of flavivirus infection. It is formed between 20 and 40 min after NS1 is synthesized and before the protein passes the Golgi apparatus. Both soluble and pelletable extracellular NS1 are also found as the high-molecular-weight form.
有证据表明,登革2型病毒非结构蛋白NS1(可溶性补体结合抗原)在感染的BHK细胞和蚊细胞培养物中以稳定寡聚体的形式存在。对分离出的寡聚体的解离产物进行鉴定,并比较天然和变性NS1中N-连接聚糖的数量,这与NS1的高分子量形式是同型二聚体的观点一致。通过分析感染圣路易斯脑炎病毒或波瓦桑病毒的BHK细胞裂解物以及登革2型病毒感染的小鼠脑组织中的蛋白质,我们证明了NS1高分子量形式的出现是黄病毒感染的一个普遍特征。它在NS1合成后20至40分钟之间形成,且在该蛋白通过高尔基体之前形成。可溶性和可沉淀的细胞外NS1也以高分子量形式存在。