Matusick-Kumar L, Hurlburt W, Weinheimer S P, Newcomb W W, Brown J C, Gao M
Department of Virology, Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey 08543-4000.
J Virol. 1994 Sep;68(9):5384-94. doi: 10.1128/JVI.68.9.5384-5394.1994.
The herpes simplex virus type 1 ICP35 assembly protein is involved in the formation of viral capsids. ICP35 is encoded by the UL26.5 gene and is specifically processed by the herpes simplex virus type 1 protease encoded by the UL26 gene. To better understand the functions of ICP35 in infected cells, we have isolated and characterized an ICP35 mutant virus, delta ICP35. The mutant virus was propagated in complementing 35J cells, which express wild-type ICP35. Phenotypic analysis of delta ICP35 shows that (i) mutant virus growth in Vero cells was severely restricted, although small amounts of progeny virus was produced; (ii) full-length ICP35 protein was not produced, although autoproteolysis of the protease still occurred in mutant-infected nonpermissive cells; (iii) viral DNA replication of the mutant proceeded at wild-type levels, but only a very small portion of the replicated DNA was processed to unit length and encapsidated; (iv) capsid structures were observed in delta ICP35-infected Vero cells by electron microscopy and by sucrose sedimentation analysis; (v) assembly of VP5 into hexons of the capsids was conformationally altered; and (vi) ICP35 has a novel function which is involved in the nuclear transport of VP5.
单纯疱疹病毒1型ICP35装配蛋白参与病毒衣壳的形成。ICP35由UL26.5基因编码,并由UL26基因编码的单纯疱疹病毒1型蛋白酶特异性加工。为了更好地理解ICP35在受感染细胞中的功能,我们分离并鉴定了一种ICP35突变病毒,即ΔICP35。该突变病毒在表达野生型ICP35的互补35J细胞中增殖。对ΔICP35的表型分析表明:(i)突变病毒在Vero细胞中的生长受到严重限制,尽管产生了少量子代病毒;(ii)虽然在突变感染的非允许细胞中蛋白酶的自我切割仍会发生,但未产生全长ICP35蛋白;(iii)突变体的病毒DNA复制以野生型水平进行,但只有非常小部分复制的DNA被加工成单位长度并被包装;(iv)通过电子显微镜和蔗糖沉降分析在ΔICP35感染的Vero细胞中观察到衣壳结构;(v)VP5装配成衣壳六聚体的构象发生改变;(vi)ICP35具有一种新功能,参与VP5的核运输。