Department of Biochemistry and Molecular Biology, Colorado State University, Fort Collins, Colorado, USA.
J Virol. 2013 May;87(10):5994-6004. doi: 10.1128/JVI.03491-12. Epub 2013 Mar 20.
Positive-strand RNA viruses generally replicate in large membrane-associated complexes. For poliovirus, these replication complexes are anchored to the membrane via the viral 2B, 2C, and 3A proteins. 2C is an AAA+ family ATPase that plays a key role in host cell membrane rearrangement, is a putative helicase, and is implicated in virion assembly and packaging. However, the membrane-binding characteristics of all of these viral proteins have made it difficult to elucidate their exact roles in virus replication. We show here that small lipid bilayers known as nanodiscs can be used to chaperone the in vitro expression of soluble poliovirus 2C, 2BC, and 2BC3AB polyproteins in a membrane-bound form. ATPase assays on these proteins show that the activity of the core 2C domain is stimulated ~0-fold compared to the larger 2BC3AB polyprotein, with most of this stimulation occurring upon removal of 2B. The proteins are active over a wide range of salt concentrations, exhibit slight lipid headgroup dependence, and show significant stimulation by acetate. Our data lead to a model wherein the replication complex can be assembled with a minimally active form of 2C that then becomes fully activated by proteolytic cleavage from the adjacent 2B viroporin domain.
正链 RNA 病毒通常在大型膜相关复合物中复制。对于脊髓灰质炎病毒,这些复制复合物通过病毒 2B、2C 和 3A 蛋白锚定在膜上。2C 是一种 AAA+家族 ATP 酶,在宿主细胞膜重排中发挥关键作用,是一种假定的解旋酶,并与病毒粒子组装和包装有关。然而,所有这些病毒蛋白的膜结合特性使得难以阐明它们在病毒复制中的确切作用。我们在这里表明,小的脂质双层(称为纳米盘)可用于在膜结合形式下陪伴体外表达可溶性脊髓灰质炎病毒 2C、2BC 和 2BC3AB 多蛋白。对这些蛋白质的 ATP 酶测定表明,与较大的 2BC3AB 多蛋白相比,核心 2C 结构域的活性被刺激约 0 倍,而大部分刺激作用发生在 2B 去除后。这些蛋白质在很宽的盐浓度范围内具有活性,表现出轻微的脂质头部基团依赖性,并被乙酸盐显著刺激。我们的数据提出了一种模型,其中复制复合物可以用最小活性形式的 2C 组装,然后通过来自相邻 2B 病毒蛋白域的蛋白水解切割而完全激活。