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Plasma membrane localization and fusion inhibitory activity of the cowpox virus serpin SPI-3 require a functional signal sequence and the virus encoded hemagglutinin

机译:牛痘病毒丝氨酸蛋白酶抑制剂SPI-3的质膜定位和融合抑制活性需要功能信号序列,并且该病毒编码的血凝素

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摘要

The cowpox virus (CPV) glycoprotein serpin SPI-3, a functional protease inhibitor, and the viral hemagglutinin (HA) are required to prevent fusion of wt CPV infected cells. SPI-3 and HA from CPV infected cells co-localize to the plasma membrane and are found in extracellular enveloped virus (EEV). We also show that an N-terminal SPI-3 signal sequence, but not glycosylation, is required for membrane localization and fusion inhibition. In the absence of HA (CPVΔHA), no SPI-3 is found on the membrane and infected cells fuse. Conversely, HA from both wt CPV and CPVΔSPI-3 infections is on the membrane, indicating a requirement of HA for SPI-3 plasma membrane localization. In the absence of HA, secretion of SPI-3 or SPI-3 N-glyc(-) was markedly enhanced, suggesting HA serves to retain SPI-3 on the plasma membrane, thereby preventing cell fusion.
机译:需要牛痘病毒(CPV)糖蛋白丝氨酸蛋白酶抑制剂(Serpin SPI-3)(一种功能性蛋白酶抑制剂)和病毒血凝素(HA),以防止感染wt CPV的细胞融合。来自CPV感染细胞的SPI-3和HA共定位于质膜,并存在于细胞外被膜病毒(EEV)中。我们还表明,膜定位和融合抑制需要N端SPI-3信号序列,而不是糖基化。在没有HA(CPVΔHA)的情况下,在膜上未发现SPI-3,受感染的细胞也融合了。相反,来自野生型CPV和CPVΔSPI-3感染的HA都在膜上,这表明HA需要SPI-3质膜定位。在没有HA的情况下,SPI-3或SPI-3 N-glyc(-)的分泌显着增强,表明HA可将SPI-3保留在质膜上,从而防止细胞融合。

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