Cotten M, Weber J M
Research Institute for Molecular Pathology, Vienna, Austria.
Virology. 1995 Nov 10;213(2):494-502. doi: 10.1006/viro.1995.0022.
We have analyzed the mechanisms used by adenovirus to gain entry into the host cell. Using both virus infection and the ability of adenovirus particles to enhance polylysine/DNA uptake as a measure of virus entry, we have demonstrated that the adenovirus-encoded 23K protease is required for two functions in the infection process. A proteolytic processing of the capsid is required to generate a virus capsid that can increase membrane interactions at pH 5. We have found that forms of adenovirus capsid that have not undergone the processing reactions (immature capsids) are deficient in their ability to disrupt membranes at pH 5 and are unable to enhance the entry of polylysine/DNA complexes. A second role of the protease was revealed by experiments using inhibitors of the protease. Mature virus capsids lose their ability to enhance gene delivery and become noninfectious after exposure to inhibitors of the protease (1 microM N-ethylmaleimide, 100-300 microM copper chloride, 1 microM MDL28170, or anti-protease antiserum), suggesting that the viral protease activity is required during the cellular entry process.
我们分析了腺病毒进入宿主细胞所采用的机制。利用病毒感染以及腺病毒颗粒增强聚赖氨酸/DNA摄取的能力作为病毒进入的衡量指标,我们证明了腺病毒编码的23K蛋白酶在感染过程中发挥两种功能。衣壳的蛋白水解加工是产生一种能在pH 5时增加膜相互作用的病毒衣壳所必需的。我们发现,未经历加工反应的腺病毒衣壳形式(未成熟衣壳)在pH 5时破坏膜的能力不足,并且无法增强聚赖氨酸/DNA复合物的进入。使用蛋白酶抑制剂的实验揭示了蛋白酶的第二个作用。成熟病毒衣壳在暴露于蛋白酶抑制剂(1 microM N - 乙基马来酰亚胺、100 - 300 microM氯化铜、1 microM MDL28170或抗蛋白酶抗血清)后,失去了增强基因传递的能力并变得无感染性,这表明在细胞进入过程中需要病毒蛋白酶活性。