Centro de Biología Molecular Severo Ochoa (CSIC-UAM), Cantoblanco, Madrid, Spain.
J Virol. 2012 Oct;86(20):11013-23. doi: 10.1128/JVI.00580-12. Epub 2012 Jul 11.
Foot-and-mouth disease virus (FMDV) nonstructural protein 3A plays important roles in virus replication, virulence, and host range. In other picornaviruses, homodimerization of 3A has been shown to be relevant for its biological activity. In this work, FMDV 3A homodimerization was evidenced by an in situ protein fluorescent ligation assay. A molecular model of the FMDV 3A protein, derived from the nuclear magnetic resonance (NMR) structure of the poliovirus 3A protein, predicted a hydrophobic interface spanning residues 25 to 44 as the main determinant for 3A dimerization. Replacements L38E and L41E, involving charge acquisition at residues predicted to contribute to the hydrophobic interface, reduced the dimerization signal in the protein ligation assay and prevented the detection of dimer/multimer species in both transiently expressed 3A proteins and in synthetic peptides reproducing the N terminus of 3A. These replacements also led to production of infective viruses that replaced the acidic residues introduced (E) by nonpolar amino acids, indicating that preservation of the hydrophobic interface is essential for virus replication. Replacements that favored (Q44R) or impaired (Q44D) the polar interactions predicted between residues Q44 and D32 did not abolish dimer formation of transiently expressed 3A, indicating that these interactions are not critical for 3A dimerization. Nevertheless, while Q44R led to recovery of viruses that maintained the mutation, Q44D resulted in selection of infective viruses with substitution D44E with acidic charge but with structural features similar to those of the parental virus, suggesting that Q44 is involved in functions other than 3A dimerization.
口蹄疫病毒(FMDV)非结构蛋白 3A 在病毒复制、毒力和宿主范围方面发挥着重要作用。在其他小核糖核酸病毒中,已证明 3A 的同源二聚化与其生物学活性有关。在这项工作中,通过原位蛋白荧光连接测定证实了 FMDV 3A 的同源二聚化。基于脊髓灰质炎病毒 3A 蛋白的核磁共振(NMR)结构,得出的 FMDV 3A 蛋白分子模型预测,残基 25 至 44 之间的疏水面为 3A 二聚化的主要决定因素。涉及到预测有助于疏水面的残基上电荷获取的替换 L38E 和 L41E,降低了蛋白连接测定中的二聚化信号,并阻止了瞬时表达的 3A 蛋白和复制 3A N 端的合成肽中二聚体/多聚体物种的检测。这些替换还导致产生了感染性病毒,这些病毒取代了引入的酸性残基(E),由非极性氨基酸取代,表明保持疏水面对于病毒复制至关重要。有利于(Q44R)或损害(Q44D)预测的 Q44 和 D32 之间的极性相互作用的替换并没有废除瞬时表达的 3A 的二聚体形成,这表明这些相互作用对于 3A 二聚化不是关键的。然而,虽然 Q44R 导致恢复了维持突变的病毒,但 Q44D 导致选择了具有酸性电荷的带取代 D44E 的感染性病毒,但具有与亲本病毒相似的结构特征,这表明 Q44 参与了除 3A 二聚化以外的功能。