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首页> 外文期刊>Research in Veterinary Science >Domain I and II from newly emerging goose tembusu virus envelope protein functions as a dominant-negative inhibitor of virus infectivity
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Domain I and II from newly emerging goose tembusu virus envelope protein functions as a dominant-negative inhibitor of virus infectivity

机译:新出现的鹅tembusu病毒包膜蛋白的结构域I和II作为病毒感染性的显性负抑制剂

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摘要

Flavivirus envelope protein locates at the outermost surface of viral particle and mediates virus entry and fusion infection, and domains I and II of E protein play an important role in this process. In this study, we have expressed and purified goose tembusu virus (GTV) E protein domains I and II (DI/II) from E. coli, and tested conceptual approach that purified protein serves as anti-viral reagent. We found that DI/II inhibited GTV JS804 infection in BHK-21 cells in a dose-dependent manner, and this inhibition activity was achieved by binding to cell membrane specifically. Moreover, JS804 treated with DI/II specific antiserum decreased its infectivity to BHK-21 cells. Taken together, this is first to show that the purified DI/ II domain of tembusu virus expressed in E. coli was able to interfere with virus infection, which opens an avenue to develop novel anti-viral regents to prevent and eventually eradicate GTV infection. (C) 2014 Elsevier Ltd. All rights reserved.
机译:黄病毒包膜蛋白位于病毒颗粒的最外层,介导病毒进入和融合感染,E蛋白的结构域I和II在此过程中起重要作用。在这项研究中,我们已经从大肠杆菌中表达和纯化了鹅tembusu病毒(GTV)E蛋白结构域I和II(DI / II),并测试了纯化蛋白用作抗病毒试剂的概念方法。我们发现DI / II以剂量依赖的方式抑制BHK-21细胞中的GTV JS804感染,并且这种抑制活性是通过特异性结合细胞膜来实现的。而且,用DI / II特异性抗血清处理的JS804降低了其对BHK-21细胞的感染性。两者合计,这首先表明在大肠杆菌中表达的纯化的tembusu病毒的DI / II结构域能够干扰病毒感染,这为开发新的抗病毒试剂以预防并最终消除GTV感染开辟了道路。 (C)2014 Elsevier Ltd.保留所有权利。

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