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Stimulation of mammalian translation initiation factor eIF4A activity by a small molecule inhibitor of eukaryotic translation

机译:真核翻译的小分子抑制剂刺激哺乳动物翻译起始因子eIF4A的活性

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摘要

RNA helicases are the largest group of enzymes in eukaryotic RNA metabolism. The DEXD/H-box putative RNA helicases form the helicase superfamily Ⅱ, whose members are defined by seven highly conserved amino acid motifs, making specific targeting of selected members a challenging pharmacological problem. The translation initiation factor eIF4A is the prototypical DEAD-box RNA helicase that works in conjunction with eIF4B and eIF4H and as a subunit of eIF4F to prepare the mRNA template for ribosome binding, possibly by unwinding the secondary structure proximal to the 5′ m~7GpppN cap structure. We report the identification and characterization of a small molecule inhibitor of eukaryotic translation initiation that acts in an unusual manner by stimulating eIF4A-associated activities. Our results suggest that proper control of eIF4A helicase activity is necessary for efficient ribosome binding and demonstrate the feasibility of selectively targeting DEAD-box RNA helicases with small molecules.
机译:RNA解旋酶是真核RNA代谢中最大的一组酶。 DEXD / H-box推定的RNA解旋酶形成了解旋酶超家族Ⅱ,其成员由七个高度保守的氨基酸基序定义,这使得针对特定成员的特异性靶向成为一个具有挑战性的药理问题。翻译起始因子eIF4A是典型的DEAD-box RNA解旋酶,可与eIF4B和eIF4H协同工作,并作为eIF4F的亚基,以准备用于核糖体结合的mRNA模板,可能是通过展开5'm〜7GpppN附近的二级结构帽盖结构。我们报告鉴定和鉴定的真核翻译起始小分子抑制剂,其通过刺激eIF4A相关的活动以不寻常的方式起作用。我们的结果表明正确控制eIF4A解旋酶活性对于有效的核糖体结合是必要的,并证明了以小分子选择性靶向DEAD-box RNA解旋酶的可行性。

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