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Identification and characterization of two conserved G-quadruplex forming motifs in the Nipah virus genome and their interaction with G-quadruplex specific ligands

机译:NIPAH病毒基因组中两个保守的G-四逆转带形成基序的鉴定与表征及其与G - Quadreplefic配体的相互作用

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The G-quadruplex (GQ) motifs are considered as potential drug-target sites for several human pathogenic viruses such as Zika, Hepatitis, Ebola, and Human Herpesviruses. The recent outbreaks of Nipah virus (NiV) in India, the highly fatal emerging zoonotic virus is a potential threat to global health security as no anti-viral drug or vaccine in currently available. Therefore, here in the present study, we sought to assess the ability of the putative G-quadruplex forming sequences in the NiV genome to form G-quadruplex structures and act as targets for anti-viral compounds. Bioinformatics analysis underpinned by various biophysical and biochemical techniques (such as NMR, CD, EMSA, DMS footprinting assay) confirmed the presence of two highly conserved G-quadruplex forming sequences (HGQs) in the G and L genes of NiV. These genes encode the cell attachment glycoprotein and RNA-dependent RNA polymerase, respectively and are essential for the virus entry and replication within the host cell. It remains possible that stabilization of these HGQs by the known G-quadruplex binding ligands like TMPyP4 and Braco-19 represents a promising strategy to inhibit the expression of the HGQ harboring genes and thereby stop the viral entry and replication inside the host cell. Accordingly, we report for the first time, that HGQs in Nipah virus genome are targets for G-quadruplex specific ligands; therefore, could serve as potential targets for anti-viral therapy.
机译:G-Quadruplex(GQ)基序被认为是几种人致病病毒的潜在药物 - 靶位点,例如Zika,肝炎,埃博拉和人疱疹病毒。印度最近爆发的NIPAH病毒(NIV)爆发,高致命的新兴的动物质病毒是对全球健康保障的潜在威胁,而目前没有抗病毒药物或疫苗。因此,在本研究中,我们试图评估核苷酸基因组中推定的G-Quadreplex形成序列以形成G-四驱结构并用作抗病毒化合物的靶标的能力。生物信息学分析由各种生物物理和生化技术(如NMR,CD,EMSA,DMS足迹测定)证实了NIV的G和L基因的两个高度保守的G-Quadreplex形成序列(HGQs)。这些基因分别编码细胞附着糖蛋白和RNA依赖性RNA聚合酶,并且对于宿主细胞内的病毒进入和复制是必不可少的。通过类似于TMPYP4和Braco-19这样的已知的G-Quadflex结合配体稳定这些HGQs的稳定性代表了抑制HGQ含有基因的表达的有希望的策略,从而阻止宿主细胞内的病毒进入和复制。因此,我们首次报告,NIPAH病毒基因组中的HGQ是G-Quadrepleficle特异性配体的靶标;因此,可以作为抗病毒治疗的潜在目标。

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