首页> 美国卫生研究院文献>Journal of Virology >G100R Mutation within 4070A Murine Leukemia Virus Env Increases Virus Receptor Binding Kinetics of Entry and Viral Transduction Efficiency
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G100R Mutation within 4070A Murine Leukemia Virus Env Increases Virus Receptor Binding Kinetics of Entry and Viral Transduction Efficiency

机译:4070A鼠白血病病毒Env中的G100R突变可增加病毒受体结合进入动力学和病毒转导效率

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摘要

Passage of 4070A murine leukemia virus (MuLV) in D17 cells resulted in a G-to-R change at position 100 within the VRA of the envelope protein (Env). Compared with 4070A MuLV, virus with the G100R Env displayed enhanced binding on target cells, internalized the virus more rapidly, and increased the overall viral titer in multiple cell types. This provides a direct correlation between binding strength and efficiency of viral entry. Deletion of a His residue at the SU N terminus eliminated the transduction efficiency by the G100R virus, suggesting that the G100R virus maintains the regulatory characteristics of 4070A viral entry. The improved transduction efficiency of G100R Env would be an asset for gene delivery systems.
机译:D17细胞中4070A鼠白血病病毒(MuLV)的传代导致包膜蛋白(Env)的VRA内100位的G-to-R变化。与4070A MuLV相比,带有G100R Env的病毒显示出与靶细胞的结合增强,使病毒内在化的速度更快,并增加了多种细胞类型的总体病毒滴度。这提供了结合强度和病毒进入效率之间的直接关联。在SU N末端缺失His残基消除了G100R病毒的转导效率,这表明G100R病毒保持了4070A病毒进入的调节特性。 G100R Env转导效率的提高将成为基因传递系统的资产。

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