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口蹄疫病毒RNA依赖的RNA聚合酶的纯化与鉴定

Purification and identification of the RNA-dependent RNA polymerase of foot-and-mouth disease virus.

作者信息

Newman J F, Cartwright B, Doel T R, Brown F

出版信息

J Gen Virol. 1979 Nov;45(2):497-507. doi: 10.1099/0022-1317-45-2-497.

Abstract

The RNA-dependent RNA polymerase induced in BHK 21 cells by infection with foot-and-mouth disease virus has been isolated from the replication complex. It contains a major, virus-coded protein with mol. wt. 56 000 which appears from serological studies and tryptic peptide mapping to be the same as the virus infection associated (VIA) antigen and the protein P56 found in cells infected with the virus. Other virus coded proteins and a host cell protein were present in the partially purified replication complex but were removed by digestion with ribonuclease T1, leaving only the major virus coded protein. The tryptic peptide maps of the VIA antigen of the seven serotypes of the virus were similar, suggesting a high level of conservation in that region of the genome coding for the RNA polymerase of each type.

摘要

通过口蹄疫病毒感染在BHK 21细胞中诱导产生的RNA依赖性RNA聚合酶已从复制复合物中分离出来。它含有一种主要的、病毒编码的蛋白质,分子量为56000,血清学研究和胰蛋白酶肽图谱分析表明,该蛋白质与病毒感染相关(VIA)抗原以及在感染该病毒的细胞中发现的P56蛋白相同。部分纯化的复制复合物中还存在其他病毒编码蛋白和一种宿主细胞蛋白,但用核糖核酸酶T1消化后这些蛋白被去除,仅留下主要的病毒编码蛋白。该病毒七种血清型的VIA抗原的胰蛋白酶肽图谱相似,这表明在编码每种类型RNA聚合酶的基因组区域具有高度保守性。

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