Inhibitory properties of nucleic acid-binding ligands on protein synthesis

被引:22
|
作者
Malina, A
Khan, S
Carlson, CB
Svitkin, Y
Harvey, I
Sonenberg, N
Beal, PA
Pelletier, J
机构
[1] McGill Univ, Dept Biochem, Montreal, PQ H3G 1Y6, Canada
[2] Univ Utah, Dept Chem, Salt Lake City, UT 84112 USA
[3] McGill Univ, McGill Canc Ctr, Montreal, PQ H3G 1Y6, Canada
来源
FEBS LETTERS | 2005年 / 579卷 / 01期
关键词
protein synthesis inhibition; nucleic acid intercalator; translation; Hepatitis C virus internal ribosome entry site;
D O I
10.1016/j.febslet.2004.06.103
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The use of small molecule inhibitors in the study of cellular processes is a powerful approach to understanding gene function. During the course of a high throughput screen for novel inhibitors of eukaryotic translation, we identified a number of nucleic acid binding ligands that showed activity in our assay. When tested on a panel of mRNA transcripts displaying different modes of translation initiation, these ligands showed a range of biological activities - with some inhibiting both cap-dependent and internal initiation and others preferentially blocking internal initiation. We used this information to identify a novel threading intercalator that inhibits Hepatitis C virus internal initiation. (C) 2004 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:79 / 89
页数:11
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