首页> 美国卫生研究院文献>Journal of Virology >Inhibition of Cellular Protein Synthesis by Simultaneous Pretreatment of Host Cells with Fowl Plague Virus and Actinomycin D: a Method for Studying Early Protein Synthesis of Several RNA Viruses
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Inhibition of Cellular Protein Synthesis by Simultaneous Pretreatment of Host Cells with Fowl Plague Virus and Actinomycin D: a Method for Studying Early Protein Synthesis of Several RNA Viruses

机译:通过禽瘟病毒和放线菌素D同时预处理宿主细胞来抑制细胞蛋白质合成:研究几种RNA病毒早期蛋白质合成的方法

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摘要

A method is described for analysis of viral protein synthesis early after infection when minute amounts of viral proteins are effectively concealed by large amounts of produced host-specific proteins. The method is superior to a radioimmune assay, since all virus-induced proteins can be measured independent of their immunological reactivity. Host-specific protein synthesis can be suppressed by infection with fowl plague virus. Addition of actinomycin D 1.25 h postinfection does not prevent this suppression, but it does block effectively the formation of fowl plague virus-specific proteins. Such cells synthesize only small amounts of cellular proteins, as revealed by polyacrylamide electrophoresis. They can be superinfected with several different enveloped viruses, however, without significant diminution of virus yields. In pretreated cells the eclipse is shortened for Semliki Forest virus, Sindbis virus, and vesicular stomatitis virus, but prolonged for Newcastle disease virus. The onset of protein synthesis, specific for the superinfecting virus, could be clearly demonstrated within 1 h after superinfection. At this time, in cells superinfected with Semliki Forest virus, great amounts of NSP 78 (nonstructural protein; molecular weight, 78 × 103) and reduced amounts of the core protein C could be demonstrated. The precursor glycoprotein NSP 68 is followed by a new polypeptide, NSP 65; three proteins with molecular weights exceeding 100 × 103 were observed which are missing later in the infectious cycle. Similar results were obtained after superinfection with Sindbis virus. The formation of a new polypeptide with a molecular weight of about 80 × 103 was detected. After superinfection with vesicular stomatitis virus or Newcastle disease virus the formation of new proteins, characteristic for the early stage of infection, was not observed.
机译:描述了一种用于在感染后早期进行分析的方法,该方法可以通过大量产生的宿主特异性蛋白有效地掩盖微量的病毒蛋白。该方法优于放射免疫测定法,因为所有病毒诱导的蛋白质均可独立于其免疫反应性进行测量。宿主特异性蛋白合成可以通过感染禽瘟病毒来抑制。感染后1.25 h加入放线菌素D并不能阻止这种抑制作用,但是它确实能有效阻止禽瘟病毒特异性蛋白的形成。如聚丙烯酰胺电泳所揭示的,这种细胞仅合成少量的细胞蛋白。它们可以用几种不同的包膜病毒进行超级感染,但是不会明显降低病毒产量。在经过预处理的细胞中,Semliki Forest病毒,Sindbis病毒和水泡性口炎病毒的食期缩短,而Newcastle病病毒的食期延长。在超级感染后1小时内,可以清楚地证明特异于超级感染病毒的蛋白质合成的开始。此时,在被Semliki Forest病毒超感染的细胞中,可以证明大量的NSP 78(非结构蛋白;分子量78×10 3 )和核心蛋白C的减少。前体糖蛋白NSP 68之后是新多肽NSP 65;观察到三种分子量超过100×10 3 的蛋白质,它们在感染周期的后期丢失。用辛德比斯病毒超级感染后获得了相似的结果。检测到新的分子量为80×10 3 的多肽的形成。在水泡性口炎病毒或新城疫病毒重感染后,未观察到新蛋白的形成,这是感染早期的特征。

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