International Centre for Genetic Engineering and Biotechnology, Padriciano 99, 34012 Trieste, Italy.
Virol J. 2011 Jan 19;8:25. doi: 10.1186/1743-422X-8-25.
The Influenza A virus non-structural protein 1 (NS1) is a multifunctional virulence factor with several protein-protein interaction domains, involved in preventing apoptosis of the infected cell and in evading the interferon response. In addition, the majority of influenza A virus NS1 proteins have a class I PDZ-binding motif at the C-terminus, and this itself has been shown to be a virulence determinant.In the majority of human influenza NS1 proteins the consensus motif is RSxV: in avian NS1 it is ESxV. Of the few human strains that have the avian motif, all were from very high mortality outbreaks of the disease. Previous work has shown that minor differences in PDZ-binding motifs can have major effects on the spectrum of cellular proteins targeted. In this study we analyse the effect of these differences upon the binding of Influenza A virus NS1 protein to a range of cellular proteins involved in polarity and signal transduction.
甲型流感病毒非结构蛋白 1(NS1)是一种多功能毒力因子,具有多个蛋白-蛋白相互作用域,参与阻止感染细胞凋亡和逃避干扰素反应。此外,大多数甲型流感病毒 NS1 蛋白在 C 末端具有一个 I 类 PDZ 结合基序,该基序本身已被证明是一个毒力决定因素。在大多数人类流感 NS1 蛋白中,共识基序为 RSxV:在禽 NS1 中为 ESxV。少数具有禽源基序的人类菌株均来自疾病高死亡率的爆发。先前的工作表明,PDZ 结合基序的微小差异可能对靶向的细胞蛋白谱产生重大影响。在这项研究中,我们分析了这些差异对甲型流感病毒 NS1 蛋白与一系列参与极性和信号转导的细胞蛋白结合的影响。