Farnsworth Aaron, Wisner Todd W, Johnson David C
Dept. of Molecular Microbiology and Immunology, Oregon Health and Science University, 3181 SW Sam Jackson Park Rd., Portland, OR 97239, USA.
J Virol. 2007 Jan;81(1):319-31. doi: 10.1128/JVI.01842-06. Epub 2006 Oct 11.
The final assembly of herpes simplex virus (HSV) involves binding of tegument-coated capsids to viral glycoprotein-enriched regions of the trans-Golgi network (TGN) as enveloped virions bud into TGN membranes. We previously demonstrated that HSV glycoproteins gE/gI and gD, acting in a redundant fashion, are essential for this secondary envelopment. To define regions of the cytoplasmic (CT) domain of gE required for secondary envelopment, HSVs lacking gD and expressing truncated gE molecules were constructed. A central region (amino acids 470 to 495) of the gE CT domain was important for secondary envelopment, although more C-terminal residues also contributed. Tandem affinity purification (TAP) proteins including fragments of the gE CT domain were used to identify tegument proteins VP22 and UL11 as binding partners, and gE CT residues 470 to 495 were important in this binding. VP22 and UL11 were precipitated from HSV-infected cells in conjunction with full-length gE and gE molecules with more-C-terminal residues of the CT domain. gD also bound VP22 and UL11. Expression of VP22 and gD or gE/gI in cells by use of adenovirus (Ad) vectors provided evidence that other viral proteins were not necessary for tegument/glycoprotein interactions. Substantial quantities of VP22 and UL11 bound nonspecifically onto or were precipitated with gE and gD molecules lacking all CT sequences, something that is very unlikely in vivo. VP16 was precipitated equally whether gE/gI or gD was present in extracts or not. These observations illustrated important properties of tegument proteins. VP22, UL11, and VP16 are highly prone to binding nonspecifically to other proteins, and this did not represent insolubility during our assays. Rather, it likely reflects an inherent "stickiness" related to the formation of tegument. Nevertheless, assays involving TAP proteins and viral proteins expressed by HSV and Ad vectors supported the conclusion that VP22 and UL11 interact specifically with the CT domains of gD and gE.
单纯疱疹病毒(HSV)的最终组装过程包括被膜包裹的衣壳与反式高尔基体网络(TGN)富含病毒糖蛋白的区域结合,此时包膜病毒粒子芽生进入TGN膜中。我们之前证明,HSV糖蛋白gE/gI和gD以冗余方式发挥作用,对于这种二次包膜化至关重要。为了确定二次包膜化所需的gE胞质(CT)结构域区域,构建了缺失gD并表达截短gE分子的HSV。gE CT结构域的一个中央区域(氨基酸470至495)对二次包膜化很重要,尽管更多的C末端残基也有贡献。包括gE CT结构域片段的串联亲和纯化(TAP)蛋白被用于鉴定被膜蛋白VP22和UL11作为结合伴侣,并且gE CT残基470至495在这种结合中很重要。VP22和UL11与全长gE以及具有CT结构域更多C末端残基的gE分子一起从HSV感染的细胞中沉淀出来。gD也与VP22和ULl1结合。通过使用腺病毒(Ad)载体在细胞中表达VP22和gD或gE/gI提供了证据,表明其他病毒蛋白对于被膜/糖蛋白相互作用不是必需的。大量的VP22和UL11非特异性地结合到缺乏所有CT序列的gE和gD分子上或与之一起沉淀,这在体内是极不可能的。无论提取物中是否存在gE/gI或gD,VP16都能同样地沉淀出来。这些观察结果说明了被膜蛋白的重要特性。VP22、UL11和VP16极易非特异性地与其他蛋白结合,而这在我们的实验中并不代表不溶性。相反,这可能反映了与被膜形成相关的内在“粘性”。然而,涉及TAP蛋白以及由HSV和Ad载体表达病毒蛋白的实验支持了VP22和UL11与gD和gE的CT结构域特异性相互作用的结论。