Andrés G, Alejo A, Simón-Mateo C, Salas M L
Centro de Biologia Molecular Severo Ochoa (Consejo Superior de Investigaciones Cientificas-Universidad Autónoma de Madrid), Universidad Autónoma, Cantoblanco, 28049 Madrid, Spain.
J Biol Chem. 2001 Jan 5;276(1):780-7. doi: 10.1074/jbc.M006844200.
African swine fever virus (ASFV) is a complex DNA virus that employs polyprotein processing at Gly-Gly-Xaa sites as a strategy to produce several major core components of the viral particle. The virus gene S273R encodes a 31-kDa protein that contains a "core domain" with the conserved catalytic residues characteristic of SUMO-1-specific proteases and the adenovirus protease. Using a COS cell expression system, it was found that protein pS273R is capable of cleaving the viral polyproteins pp62 and pp220 in a specific way giving rise to the same intermediates and mature products as those produced in ASFV-infected cells. Furthermore, protein pS273R, like adenovirus protease and SUMO-1-specific enzymes, is a cysteine protease, because its activity is abolished by mutation of the predicted catalytic histidine and cysteine residues and is inhibited by sulfhydryl-blocking reagents. Protein pS273R is expressed late after infection and is localized in the cytoplasmic viral factories, where it is found associated with virus precursors and mature virions. In the virions, the protein is present in the core shell, a domain where the products of the viral polyproteins are also located. The identification of the ASFV protease will allow a better understanding of the role of polyprotein processing in virus assembly and may contribute to our knowledge of the emerging family of SUMO-1-specific proteases.
非洲猪瘟病毒(ASFV)是一种复杂的DNA病毒,它利用在甘氨酸-甘氨酸-Xaa位点进行多蛋白加工作为产生病毒颗粒几个主要核心成分的策略。病毒基因S273R编码一种31 kDa的蛋白质,该蛋白质含有一个“核心结构域”,具有与SUMO-1特异性蛋白酶和腺病毒蛋白酶特征性的保守催化残基。使用COS细胞表达系统发现,蛋白质pS273R能够以特定方式切割病毒多蛋白pp62和pp220,产生与ASFV感染细胞中产生的相同中间体和成熟产物。此外,蛋白质pS273R与腺病毒蛋白酶和SUMO-1特异性酶一样,是一种半胱氨酸蛋白酶,因为其活性通过预测的催化组氨酸和半胱氨酸残基的突变而被消除,并被巯基阻断试剂抑制。蛋白质pS273R在感染后期表达,定位于细胞质病毒工厂,在那里发现它与病毒前体和成熟病毒粒子相关。在病毒粒子中,该蛋白质存在于核心壳中,病毒多蛋白的产物也位于该区域。ASFV蛋白酶的鉴定将有助于更好地理解多蛋白加工在病毒组装中的作用,并可能有助于我们了解新兴的SUMO-1特异性蛋白酶家族。