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Functional incorporation of green fluorescent protein into hepatitis B virus envelope particles

机译:将绿色荧光蛋白功能性掺入乙肝病毒包膜颗粒

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摘要

The envelope of hepatitis B virus (HBV), containing the L, M, and S proteins, is essential for virus entry and maturation. For direct visualization of HBV, we determined whether envelope assembly could accommodate the green fluorescent protein (GFP). While the C-terminal addition of GFP to S trans-dominant negatively inhibited empty envelope particle secretion, the N-terminal GFP fusion to S (GFP.S) was co-integrated into the envelope, giving rise to fluorescent particles. Microscopy and topogenesis analyses demonstrated that the proper intracellular distribution and folding of GFP.S, required for particle export were rescued by interprotein interactions with wild-type S. Thereby, a dual location of GFP, inside and outside the envelope, was observed. GFP.S was also efficiently packaged into the viral envelope, and these GFP-tagged virions retained the capacity for attachment to HBV receptor-positive cells in vitro. Together, GFP-tagged virions should be suitable to monitor HBV uptake and egress in live hepatocytes.
机译:包含L,M和S蛋白的乙型肝炎病毒(HBV)的包膜对于病毒进入和成熟至关重要。为了直接观察HBV,我们确定了包膜组件是否可以容纳绿色荧光蛋白(GFP)。当GFP的C末端添加到S反式显着抑制空包膜颗粒的分泌时,N末端的GFP与S的融合(GFP.S)被共整合到外壳中,产生荧光颗粒。显微镜检查和拓扑分析表明,通过与野生型S的蛋白间相互作用,拯救了颗粒输出所需的GFP.S在细胞内的适当分布和折叠。从而观察到GFP在包膜内部和外部的双重位置。 GFP.S也被有效地包装到病毒包膜中,这些带有GFP标签的病毒粒子在体外仍具有附着于HBV受体阳性细胞的能力。带有GFP标记的病毒粒子一起应适合监测活肝细胞中HBV的摄取和流出。

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