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Discovery of direct-acting antiviral agents with a graphene-based fluorescent nanosensor

机译:用基于石墨烯的荧光纳米传感器发现直效抗病毒试剂

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Direct-acting agents against viral components are considered as the most promising candidates for the successful antiviral therapeutics. To date, no direct-acting drugs exist for the treatment against dengue virus (DV) infection, which can develop into life-threatening diseases. RNA-dependent RNA polymerase (RdRp), an RNA virus–specific enzyme highly conserved among various viral families, has been known as the broad-range antiviral drug target. Here, we developed an RNA-based graphene biosensor system [RNA nano-graphene oxide system (RANGO)] to enable the fluorescence-based quantitative analysis of the RdRp enzyme activity. We used the RANGO system to a high-throughput chemical screening to identify novel direct-acting antiviral drug candidates targeting DV RdRp from the FDA-approved small-molecule library. RANGO accelerated the massive selection of drug candidates. We found that one of the selected hit compounds, montelukast, showed antiviral activity in vitro and in vivo by directly inhibiting replication of DV and thus relieved related symptoms.
机译:针对病毒组分的直接作用剂被认为是成功抗病毒治疗的最有希望的候选人。迄今为止,没有用于治疗登革热病毒(DV)感染的直接药物,这可以发展成为危及生命的疾病。 RNA依赖性RNA聚合酶(RDRP)是各种病毒家族中高度保守的RNA病毒特异性酶被称为广泛的抗病毒品靶标。在此,我们开发了一种基于RNA的石墨烯生物传感器系统[RNA纳米石墨烯氧化物系统(RANGO)],以实现RDRP酶活性的荧光的定量分析。我们将rango系统用于高通量化学筛选,以鉴定来自FDA批准的小分子库的DV RDRP的新型直接抗病毒品候选物。 rango加速了大量选择的药物候选人。我们发现,通过直接抑制DV的复制并因此通过直接抑制DV的复制并因此释放相关症状,因此在体外和体内显示出抗病毒活性。

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