Integrated Program in Biomedical Sciences, University of Tennessee Health Science Center, Memphis, Tennessee 38163, United States.
ACS Chem Biol. 2012 Mar 16;7(3):526-34. doi: 10.1021/cb200439z. Epub 2012 Jan 19.
Influenza viruses have been responsible for the largest pandemics in the previous century. Although vaccination and prophylactic antiviral therapeutics are the primary defense against influenza virus, there is a pressing need to develop new antiviral agents to circumvent the limitations of current therapies. The endonuclease activity of the influenza virus PA(N) protein is essential for virus replication and is a promising target for novel anti-influenza drugs. To facilitate the discovery of endonuclease inhibitors, we have developed a high-throughput fluorescence polarization (FP) assay, utilizing a novel fluorescein-labeled compound (K(d) = 0.378 μM) and a PA(N) construct, to identify small molecules that bind to the PA(N) endonuclease active site. Several known 4-substituted 2,4-dioxobutanoic acid inhibitors with high and low affinities have been evaluated in this FP-based competitive binding assay, and there was a general correlation between binding and the reported inhibition of endonuclease activity. Additionally, we have demonstrated the utility of this assay for identifying endonuclease inhibitors in a small diverse targeted fragment library. These fragment hits were used to build a follow-up library that that led to new active compounds that demonstrate FP binding and anti-influenza activities in plaque inhibition assays. The assay offers significant advantages over previously reported assays and is suitable for high-throughput and fragment-based screening studies. Additionally the demonstration of the applicability of a mechanism-based "targeted fragment" library supports the general potential of this novel approach for other enzyme targets. These results serve as a sound foundation for the development of new therapeutic leads targeting influenza endonuclease.
流感病毒是上世纪引发最大规模流感疫情的罪魁祸首。虽然疫苗接种和预防性抗病毒疗法是预防流感病毒的主要手段,但开发新的抗病毒药物以规避当前疗法的局限性仍然迫在眉睫。流感病毒 PA(N) 蛋白的内切核酸酶活性对病毒复制至关重要,是新型抗流感药物的一个有前途的靶标。为了促进内切核酸酶抑制剂的发现,我们开发了一种高通量荧光偏振(FP)测定法,利用一种新型荧光素标记化合物(Kd = 0.378 μM)和 PA(N) 构建体,以鉴定与 PA(N) 内切核酸酶活性位点结合的小分子。几种具有高亲和力和低亲和力的已知 4-取代 2,4-二氧代丁酸抑制剂已在这种基于 FP 的竞争性结合测定中进行了评估,并且结合与报道的内切核酸酶活性抑制之间存在普遍相关性。此外,我们还证明了该测定法在鉴定小而多样化的靶向片段文库中的内切核酸酶抑制剂方面的实用性。这些片段命中物被用于构建后续文库,这些文库产生了新的活性化合物,在蚀斑抑制测定中表现出 FP 结合和抗流感活性。与之前报道的测定法相比,该测定法具有显著优势,适用于高通量和基于片段的筛选研究。此外,基于机制的“靶向片段”文库适用性的证明支持了这种新方法在其他酶靶标中的普遍潜力。这些结果为开发针对流感内切核酸酶的新型治疗先导物奠定了坚实的基础。