首页> 外文期刊>Journal of Medical Virology >Cloning, sequencing, and expression of the hepatitis E virus (HEV) nonstructural open reading frame 1 (ORF1).
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Cloning, sequencing, and expression of the hepatitis E virus (HEV) nonstructural open reading frame 1 (ORF1).

机译:戊型肝炎病毒(HEV)非结构性开放阅读框1(ORF1)的克隆,测序和表达。

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摘要

Hepatitis E virus (HEV) causes enterically transmitted epidemic and sporadic viral hepatitis affecting millions of people in the developing world. Different geographical isolates of HEV show a high degree of homology at the nucleotide and amino acid levels. The approximately 7.2 kb RNA genome has three open reading frames of which ORF1 is predicted to code for the viral nonstructural polyprotein. The expression, processing and properties of the nonstructural ORF1 polyprotein have not been reported so far. In this study, the complete HEV ORF1 was reconstructed from overlapping fragments amplified by polymerase chain reaction (PCR) of total RNA isolated from the bile fluid of a rhesus monkey experimentally infected with HEV isolate from an epidemic. The complete assembled ORF1 was sequenced using HEV specific primers. The ORF1 polyprotein was expressed in E. coli, in a cell free translation system and in HepG2 cells, and was characterized by western blotting and immunoprecipitation using acute phase patient serum as well as polyclonal antibodies raised against defined parts of the ORF1 polyprotein. The nonstructural polyprotein of HEV was expressed as a 186 kDa protein. No processing was observed into discrete units, either in-vitro based on a kinetic analysis, or in HepG2 cells based on immunoprecipitation. Copyright 2000 Wiley-Liss, Inc.
机译:戊型肝炎病毒(HEV)导致肠道传播的流行病和散发性病毒性肝炎,影响了发展中国家的数百万人。 HEV的不同地理分离株在核苷酸和氨基酸水平上显示高度同源性。大约7.2 kb的RNA基因组具有三个开放阅读框,其中ORF1被预测为编码病毒非结构多蛋白。到目前为止,尚未报道非结构性ORF1多蛋白的表达,加工和特性。在这项研究中,完整的戊型肝炎病毒ORF1是从重叠片段中重建的,该重叠片段是通过从总RNA中分离得到的总RNA的聚合酶链反应(PCR)扩增而得到的,该RNA从实验上感染了流行病的戊型肝炎病毒的恒河猴的胆汁中分离出来。使用HEV特异性引物对完整组装的ORF1进行测序。 ORF1多蛋白在大肠杆菌,无细胞翻译系统和HepG2细胞中表达,其特征在于使用急性期患者血清以及针对ORF1多蛋白定义部分的多克隆抗体进行蛋白质印迹和免疫沉淀。 HEV的非结构性多蛋白表达为186 kDa蛋白。基于动力学分析在体外或基于免疫沉淀的HepG2细胞中均未观察到加工成离散单元的过程。版权所有2000 Wiley-Liss,Inc.

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