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Adriamycin inhibits human RH II/Gu RNA helicase activity by binding to its substrate.
Zhu, K; Henning, D; Iwakuma, T; Valdez, B C; Busch, H.
Afiliação
  • Zhu K; Department of Pharmacology, Baylor College of Medicine, One Baylor Plaza, Houston, Texas 77030, USA.
Biochem Biophys Res Commun ; 266(2): 361-5, 1999 Dec 20.
Article em En | MEDLINE | ID: mdl-10600508
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.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doxorrubicina / RNA Helicases / Proteínas Modificadoras Pequenas Relacionadas à Ubiquitina Limite: Humans Idioma: En Revista: Biochem Biophys Res Commun Ano de publicação: 1999 Tipo de documento: Article País de afiliação: Estados Unidos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doxorrubicina / RNA Helicases / Proteínas Modificadoras Pequenas Relacionadas à Ubiquitina Limite: Humans Idioma: En Revista: Biochem Biophys Res Commun Ano de publicação: 1999 Tipo de documento: Article País de afiliação: Estados Unidos
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