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.