Aboud M, Shoor R, Salzberg S
J Gen Virol. 1980 Dec;51(Pt 2):425-9. doi: 10.1099/0022-1317-51-2-425.
Adsorption of murine leukaemia virus (MLV) to NIH/3T3 cells, as determined by analysing its reverse transcriptase activity in the cell membrane, was found to be unaffected by interferon (IFN). Virus penetration and uncoating were followed by quantifying intracellular virions in terms of sedimentable reverse transcriptase activity in the cytoplasmic fraction. The penetrating virions were found to accumulate to a higher level in IFN-treated cells than in untreated controls. Intracellular virions were uncoated in untreated cells shortly after their penetration, whereas their uncoating was delayed in the IFN-treated cells for 2 to 3 h. Neither virus uncoating nor the effect of IFN on this process appeared to require new protein synthesis, since both were unaffected by cycloheximide (CH).
通过分析细胞膜中鼠白血病病毒(MLV)的逆转录酶活性来确定其对NIH/3T3细胞的吸附,结果发现其不受干扰素(IFN)影响。通过根据细胞质部分中可沉降的逆转录酶活性对细胞内病毒粒子进行定量来追踪病毒的穿透和脱壳过程。结果发现,与未处理的对照相比,穿透的病毒粒子在经IFN处理的细胞中积累到更高水平。细胞内病毒粒子在穿透后不久就在未处理的细胞中脱壳,而在经IFN处理的细胞中其脱壳延迟2至3小时。病毒脱壳以及IFN对该过程的影响似乎均不需要新的蛋白质合成,因为二者均不受环己酰亚胺(CH)的影响。