Cudmore S, Blasco R, Vincentelli R, Esteban M, Sodeik B, Griffiths G, Krijnse Locker J
Cell Biology Program, European Molecular Biology Laboratory, Heidelberg, Germany.
J Virol. 1996 Oct;70(10):6909-21. doi: 10.1128/JVI.70.10.6909-6921.1996.
We describe herein the characterization of p39, the product of the A4L gene of vaccinia virus. By immunolabelling of thawed cryosections from infected HeLa cells, we show that this protein is initially located in the central region, or viroplasm, of the viral factories, as well as in the immature virions, with very small amounts of labelling observed on the surrounding membranes. The localization of p39 changes dramatically during the transition of the immature virion to the intracellular mature virus (IMV), coincident with the appearance of the core structure in the center of the IMV, with p39 located between this core and the surrounding membranes. Complementary biochemical data, such as partitioning into the Triton X-114 detergent phase and stripping of the viral membranes with Nonidet P-40 and dithiothreitol, suggest that p39 is associated with the innermost of the two membranes surrounding the core. Sodium carbonate treatment also indicates that p39 is associated with membranes, even at the early stages of viral assembly. However, following in vitro translation of p39 in the presence of microsomal membranes, we failed to detect any association of the independently expressed protein with membranes. We also failed to detect any posttranslational acylation of p39 with myristate or palmitate, suggesting that p39 does not achieve its membrane association through lipid anchors. Therefore, p39 is most likely membrane associated through an interaction with an integral membrane protein(s) present in the innermost of the two membranes surrounding the IMV. These data, together with our recent data showing that p39 colocalizes with the spike-like protrusions on the IMV core (N. Roos, M. Cyrklaff, S. Cudmore, R. Blasco, J. Krijnse-Locker, and G. Griffiths, EMBO J. 15:2343-2355, 1996), suggest that p39 may form part of this spike and that it possibly functions as a matrix-like linker protein between the core and the innermost of the two membranes surrounding the IMV.
我们在此描述痘苗病毒A4L基因产物p39的特性。通过对感染的HeLa细胞解冻后的冰冻切片进行免疫标记,我们发现该蛋白最初位于病毒工厂的中心区域或病毒质中,以及未成熟病毒粒子中,在周围膜上观察到的标记量非常少。在未成熟病毒粒子向细胞内成熟病毒(IMV)转变过程中,p39的定位发生了显著变化,这与IMV中心核心结构的出现同时发生,p39位于该核心与周围膜之间。补充的生化数据,如分配到Triton X-114去污剂相中以及用Nonidet P-40和二硫苏糖醇去除病毒膜,表明p39与围绕核心的两层膜的最内层相关。碳酸钠处理也表明p39即使在病毒组装的早期阶段也与膜相关。然而,在微粒体膜存在的情况下对p39进行体外翻译后,我们未能检测到独立表达的蛋白与膜有任何关联。我们也未能检测到p39有任何肉豆蔻酸或棕榈酸的翻译后酰化,这表明p39不是通过脂质锚定实现其与膜的关联。因此,p39很可能是通过与存在于围绕IMV的两层膜最内层的一种整合膜蛋白相互作用而与膜相关。这些数据,连同我们最近的数据表明p39与IMV核心上的刺状突起共定位(N. Roos、M. Cyrklaff、S. Cudmore、R. Blasco、J. Krijnse-Locker和G. Griffiths,《欧洲分子生物学组织杂志》15:2343 - 2355,1996),表明p39可能构成这种刺的一部分,并且它可能作为IMV核心与围绕IMV的两层膜最内层之间的类似基质的连接蛋白发挥作用。