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戊型肝炎病毒(HEV)非结构开放阅读框1(ORF1)的克隆、测序及表达

Cloning, sequencing, and expression of the hepatitis E virus (HEV) nonstructural open reading frame 1 (ORF1).

作者信息

Ansari I H, Nanda S K, Durgapal H, Agrawal S, Mohanty S K, Gupta D, Jameel S, Panda S K

机构信息

Department of Pathology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, India.

出版信息

J Med Virol. 2000 Mar;60(3):275-83.

Abstract

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.

摘要

戊型肝炎病毒(HEV)引起经肠道传播的流行性和散发性病毒性肝炎,影响着发展中世界数以百万计的人口。HEV的不同地理分离株在核苷酸和氨基酸水平上显示出高度同源性。约7.2 kb的RNA基因组有三个开放阅读框,其中ORF1预计编码病毒非结构多聚蛋白。迄今为止,尚未报道非结构ORF1多聚蛋白的表达、加工及特性。在本研究中,从一只实验感染了来自一次流行的HEV分离株的恒河猴胆汁中分离的总RNA,通过聚合酶链反应(PCR)扩增的重叠片段重建了完整的HEV ORF1。使用HEV特异性引物对完整组装的ORF1进行测序。ORF1多聚蛋白在大肠杆菌、无细胞翻译系统和HepG2细胞中表达,并用急性期患者血清以及针对ORF1多聚蛋白特定部分产生的多克隆抗体进行蛋白质印迹和免疫沉淀分析。HEV的非结构多聚蛋白表达为一种186 kDa的蛋白质。基于动力学分析,在体外未观察到其加工成离散单元;基于免疫沉淀,在HepG2细胞中也未观察到。

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