Ghanem Alexander, Mayer Daniel, Chase Geoffrey, Tegge Werner, Frank Ronald, Kochs Georg, García-Sastre Adolfo, Schwemmle Martin
Department of Virology, Institute for Medical Microbiology and Hygiene, University of Freiburg, Hermann-Herder-Strasse 11, D-79104 Freiburg, Germany.
J Virol. 2007 Jul;81(14):7801-4. doi: 10.1128/JVI.00724-07. Epub 2007 May 9.
The assembly of the polymerase complex of influenza A virus from the three viral polymerase subunits PB1, PB2, and PA is required for viral RNA synthesis. We show that peptides which specifically bind to the protein-protein interaction domains in the subunits responsible for complex formation interfere with polymerase complex assembly and inhibit viral replication. Specifically, we provide evidence that a 25-amino-acid peptide corresponding to the PA-binding domain of PB1 blocks the polymerase activity of influenza A virus and inhibits viral spread. Targeting polymerase subunit interactions therefore provides a novel strategy to develop antiviral compounds against influenza A virus or other viruses.
甲型流感病毒的聚合酶复合体由三个病毒聚合酶亚基PB1、PB2和PA组装而成,这是病毒RNA合成所必需的。我们发现,特异性结合负责复合体形成的亚基中蛋白质-蛋白质相互作用结构域的肽会干扰聚合酶复合体的组装并抑制病毒复制。具体而言,我们提供的证据表明,一个对应于PB1的PA结合结构域的25个氨基酸的肽可阻断甲型流感病毒的聚合酶活性并抑制病毒传播。因此,靶向聚合酶亚基相互作用为开发针对甲型流感病毒或其他病毒的抗病毒化合物提供了一种新策略。