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阿霉素通过与底物结合来抑制人RH II/Gu RNA解旋酶的活性。

Adriamycin inhibits human RH II/Gu RNA helicase activity by binding to its substrate.

作者信息

Zhu K, Henning D, Iwakuma T, Valdez B C, Busch H

机构信息

Department of Pharmacology, Baylor College of Medicine, One Baylor Plaza, Houston, Texas 77030, USA.

出版信息

Biochem Biophys Res Commun. 1999 Dec 20;266(2):361-5. doi: 10.1006/bbrc.1999.1815.

Abstract

RNA helicases are enzymes important in RNA synthesis, processing, transport, and turnover. Human nucleolar RNA helicase II/Gu protein (RH II/Gu) was expressed in a baculovirus system. The purified recombinant RH II/Gu protein has RNA helicase activity on a 5' tailed ds RNA substrate in vitro. We found that Adriamycin, a widely used anticancer drug, inhibited RH II/Gu helicase activity in a dose-dependent manner with an IC(50) of 40 microM. Adriamycin bound to the RNA substrate, and the binding was disrupted by boiling or treatment with 1% SDS, suggesting that the binding of Adriamycin to RNA is reversible. Adriamycin was also found by gel electrophoresis to bind to yeast tRNA to form slow-migrating complexes. These results suggest that Adriamycin can inhibit RNA synthesis or processing by binding to RNA substrates.

摘要

RNA解旋酶是在RNA合成、加工、运输及周转过程中起重要作用的酶。人核仁RNA解旋酶II/Gu蛋白(RH II/Gu)在杆状病毒系统中表达。纯化的重组RH II/Gu蛋白在体外对5' 带尾双链RNA底物具有RNA解旋酶活性。我们发现,广泛使用的抗癌药物阿霉素以剂量依赖方式抑制RH II/Gu解旋酶活性,其半数抑制浓度(IC50)为40微摩尔。阿霉素与RNA底物结合,且该结合可通过煮沸或用1%十二烷基硫酸钠(SDS)处理而被破坏,这表明阿霉素与RNA的结合是可逆的。通过凝胶电泳还发现阿霉素可与酵母tRNA结合形成迁移缓慢的复合物。这些结果表明,阿霉素可通过与RNA底物结合来抑制RNA合成或加工。

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