Jensen O N, Houthaeve T, Shevchenko A, Cudmore S, Ashford T, Mann M, Griffiths G, Krijnse Locker J
Protein and Peptide Group, European Molecular Biology Laboratory, Heidelberg, Germany.
J Virol. 1996 Nov;70(11):7485-97. doi: 10.1128/JVI.70.11.7485-7497.1996.
Vaccinia virus assembly has been well studied at the ultrastructural level, but little is known about the molecular events that occur during that process. Towards this goal, we have identified the major membrane and core proteins of the intracellular mature virus (IMV). Pure IMV preparations were subjected to Nonidet P-40 (NP-40) and dithiothreitol (DTT) treatment to separate the core proteins from the membrane proteins. These proteins were subsequently separated by two-dimensional (2D) gel electrophoresis, and the major polypeptide spots, as detected by silver staining and 35S labeling, were identified by either matrix-assisted laser desorption/ionization mass spectrometry, N-terminal amino acid sequencing, or immunoprecipitation with defined antibodies. Sixteen major spots that partitioned into the NP-40-DTT-soluble fraction were identified; 11 of these were previously described virally encoded proteins and 5 were cellular proteins, mostly of mitochondrial origin. The core fraction revealed four major spots of previously described core proteins, two of which were also detected in the membrane fraction. Subsequently, the NP-40-DTT-soluble and -insoluble fractions from purified virus preparations, separated by 2D gels, were compared with postnuclear supernatants of infected cells that had been metabolically labeled at late times (6 to 8 h) postinfection. This relatively short labeling period as well as the apparent shutoff of host protein synthesis allowed the selective detection in such postnuclear supernatants of virus-encoded proteins. These postnuclear supernatants were subsequently treated with Triton X-114 or with sodium carbonate to distinguish the membrane proteins from the soluble proteins. We have identified the major late membrane and nonmembrane proteins of the IMV as they occur in the virus as well as in infected cells. This 2D gel map should provide an important reference for future molecular studies of vaccinia virus morphogenesis.
痘苗病毒的组装在超微结构水平上已得到充分研究,但对于该过程中发生的分子事件却知之甚少。为实现这一目标,我们已鉴定出细胞内成熟病毒(IMV)的主要膜蛋白和核心蛋白。将纯化的IMV制剂用非离子去污剂NP-40和二硫苏糖醇(DTT)处理,以将核心蛋白与膜蛋白分离。随后,通过二维(2D)凝胶电泳分离这些蛋白质,并用银染和35S标记检测主要多肽斑点,通过基质辅助激光解吸/电离质谱、N端氨基酸测序或用特异性抗体进行免疫沉淀来鉴定这些斑点。鉴定出16个主要斑点,它们存在于NP-40-DTT可溶性部分中;其中11个是先前描述的病毒编码蛋白,5个是细胞蛋白,大多源自线粒体。核心部分显示出先前描述的4个主要核心蛋白斑点,其中2个也在膜部分中检测到。随后,将二维凝胶分离的纯化病毒制剂的NP-40-DTT可溶性和不溶性部分,与感染后晚期(感染后6至8小时)经代谢标记的感染细胞核后上清液进行比较。这一相对较短的标记期以及宿主蛋白合成的明显关闭,使得能够在这种核后上清液中选择性检测病毒编码蛋白。随后,用Triton X-114或碳酸钠处理这些核后上清液,以区分膜蛋白和可溶性蛋白。我们已经鉴定出IMV在病毒以及感染细胞中存在的主要晚期膜蛋白和非膜蛋白。这张二维凝胶图谱应为痘苗病毒形态发生的未来分子研究提供重要参考。