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Inactivation of vesicular stomatitis virus through inhibition of membrane fusion by chemical modification of the viral glycoprotein.

机译:通过化学修饰病毒糖蛋白抑制膜融合来灭活水泡性口炎病毒。

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Membrane fusion is an essential step in the entry of enveloped viruses into their host cells triggered by conformational changes in viral glycoproteins. We have demonstrated previously that modification of vesicular stomatitis virus (VSV) with diethylpyrocarbonate (DEPC) abolished conformational changes on VSV glycoprotein and the fusion reaction catalyzed by the virus. In the present study, we evaluated whether treatment with DEPC was able to inactivate the virus. Infectivity and viral replication were abolished by viral treatment with 0.5mM DEPC. Mortality profile and inflammatory response in the central nervous system indicated that G protein modification with DEPC eliminates the ability of the virus to cause disease. In addition, DEPC treatment did not alter the conformational integrity of surface proteins of inactivated VSV as demonstrated by transmission electron microscopy and competitive ELISA. Taken together, our results suggest a potential use of histidine (His) modification to the development of a new process of viral inactivation based on fusion inhibition.
机译:膜融合是由病毒糖蛋白的构象变化触发的包膜病毒进入其宿主细胞的必不可少的步骤。先前我们已经证明,用焦碳酸二乙酯(DEPC)修饰水疱性口炎病毒(VSV)可以消除VSV糖蛋白的构象变化以及该病毒催化的融合反应。在本研究中,我们评估了用DEPC处理是否能够灭活该病毒。用0.5mM DEPC进行病毒处理可消除感染性和病毒复制。中枢神经系统的死亡率分布和炎症反应表明,DEPC对G蛋白的修饰消除了病毒引起疾病的能力。此外,DEPC处理不会改变灭活的VSV表面蛋白的构象完整性,这是通过透射电子显微镜和竞争性ELISA证明的。两者合计,我们的结果表明组氨酸(His)修饰的潜在用途,以开发基于融合抑制的病毒灭活的新过程。

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