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首页> 外文期刊>Angewandte Chemie >Design of β-Hairpin Peptidomimetics That Inhibit Binding of -Helical HIV-1 Rev Protein to the Rev Response Element RNA
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Design of β-Hairpin Peptidomimetics That Inhibit Binding of -Helical HIV-1 Rev Protein to the Rev Response Element RNA

机译:抑制-螺旋HIV-1 Rev蛋白与Rev反应元件RNA结合的β-发夹肽模拟物的设计

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摘要

The virally encoded Rev protein of human immunodeficiency virus type-1 (HIV-1) plays a critical role in viral replication by regulating the transport of unspliced and partially spliced viral RNA from the nucleus to the cytoplasm of infected cells.[1], [2] Rev binds first to a specific region of the HIV-1 mRNA, called the Rev responsive element (RRE) of stem loop IIb (Figure 1); subsequent to this initial binding event, approximately 10 additional Rev molecules oligomerize through protein-protein and protein-RNA interactions and coat the entire RRE.[3] Because of its essential role in viral replication, the interaction between Rev protein and the high-affinity RRE binding site represents an attractive yet unexploited target for antiviral therapy.
机译:1型人类免疫缺陷病毒(HIV-1)的病毒编码Rev蛋白通过调节未剪接和部分剪接的病毒RNA从细胞核到感染细胞质的转运,在病毒复制中发挥关键作用。[1],[ 2] Rev首先与HIV-1 mRNA的特定区域结合,称为茎环IIb的Rev响应元件(RRE)(图1);在此初始结合事件之后,大约有10个另外的Rev分子通过蛋白质-蛋白质和蛋白质-RNA相互作用寡聚并覆盖了整个RRE。[3]由于其在病毒复制中的重要作用,Rev蛋白与高亲和力RRE结合位点之间的相互作用代表了抗病毒治疗的诱人但尚未开发的目标。

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