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首页> 外文期刊>Molecules and cells >Recovery of TRIM25-Mediated RIG-I Ubiquitination through Suppression of NS1 by RNA Aptamers
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Recovery of TRIM25-Mediated RIG-I Ubiquitination through Suppression of NS1 by RNA Aptamers

机译:通过RNA适体抑制NS1恢复TRIM25介导的RIG-I泛素化。

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摘要

Non-structural protein 1 (NS1) of influenza virus has been shown to inhibit the innate immune response by blocking the induction of interferon (IFN). In this study, we isolated two single-stranded RNA aptamers specific to NS1 with K subd/sub values of 1.62 ± 0.30 nM and 1.97 ± 0.27 nM, respectively, using a systematic evolution of ligand by exponential enrichment (SELEX) procedure. The selected aptamers were able to inhibit the interaction of NS1 with tripartite motif-containing protein 25 (TRIM25), and suppression of NS1 enabled retinoic acid inducible gene I (RIG-I) to be ubiquitinated regularly by TRIM25. Additional luciferase reporter assay and quantitative real-time PCR (RT-PCR) experiments demonstrated that suppression of NS1 by the selected aptamers induced IFN production. It is noted that viral replication was also inhibited through IFN induction in the presence of the selected aptamers. These results suggest that the isolated aptamers are strongly expected to be new therapeutic agents against influenza infection.
机译:流感病毒的非结构蛋白1(NS1)已显示可通过阻断干扰素(IFN)的诱导而抑制先天免疫应答。在这项研究中,我们使用指数富集的系统配体进化方法(SELEX)分离了两个NS1特异的单链RNA适体,K d 的K值分别为1.62±0.30 nM和1.97±0.27 nM。 )程序。选择的适体能够抑制NS1与包含三重基序的蛋白质25(TRIM25)的相互作用,并且抑制NS1使得视黄酸诱导基因I(RIG-1)能够被TRIM25规则地泛素化。额外的荧光素酶报告基因检测和定量实时PCR(RT-PCR)实验表明,所选适体对NS1的抑制作用可诱导IFN的产生。应当指出,在所选适体存在下,病毒复制也通过IFN诱导而被抑制。这些结果表明,强烈期望分离的适体是针对流感感染的新治疗剂。

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