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HEV-ORF3 ENCODING PHOSPHOPROTEIN INTERACTS WITH HEPSIN

机译:HEV-ORF3编码磷酸蛋白与胃蛋白酶的相互作用

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Background: Hepatitis E virus (HEV) is a major causative agent of acute clinical hepatitis in adults through much of Asia, the Middle East and Africa. Open reading frame 3 (ORF3) encodes around 120 amino acids of phosphorylation protein that associates with the cytoskeleton, while its precise biological function is still unknown.Objectives: In order to understand the function of ORF3 protein (pORF3) in depth, HEV ORF3 interacting proteins were screened in human hepatocytes cDNA library using two-hybrid system techniques and further verification of the interactions were carried out through co-immunoprecipitation (Co-IP).Materials and Methods: The Cyto-Trap two-hybrid system technology, a classical method for analyzing protein interactions, was used to screen the pORF3 interacting proteins from human hepatocytes cDNA library.Results: Through the Cyto-Trap two-hybrid system, eight proteins interacting with pORF3 were winnowed. The Co-IP results confirmed that hepsin which is reported to function as the inhibitor of several tumors reacted with pORF3.Conclusions: Out of eight screened proteins interacting with pORF3, hepsin was confirmed to have specific interactions with pORF3.
机译:背景:戊型肝炎病毒(HEV)是亚洲,中东和非洲许多地区成年人急性临床肝炎的主要病原体。开放阅读框3(ORF3)编码与细胞骨架相关的约120个氨基酸的磷酸化蛋白,但其确切的生物学功能尚不清楚。目的:为了深入了解ORF3蛋白(pORF3)的功能,HEV ORF3进行了相互作用使用双重杂交系统技术在人肝细胞cDNA文库中筛选蛋白,并通过共免疫沉淀(Co-IP)进一步验证相互作用。材料与方法:经典的Cyto-Trap双重杂交系统技术为了分析蛋白质的相互作用,从人肝细胞cDNA文库中筛选了pORF3的相互作用蛋白。结果:通过Cyto-Trap两杂交系统,筛选出了8种与pORF3相互作用的蛋白。 Co-IP结果证实,据报道可作为几种肿瘤抑制剂的肝素与pORF3反应。结论:在与pORF3相互作用的8种筛选蛋白中,证实了肝素与pORF3有特异性相互作用。

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