The viral RNA capping machinery as a target for antiviral drugs

被引:80
作者
Ferron, Francois
Decroly, Etienne
Selisko, Barbara
Canard, Bruno [1 ]
机构
[1] CNRS, F-13288 Marseille 09, France
关键词
5 '-Triphosphatase; Guanylyltransferase; Methyltransferase; Endonuclease; Cap snatching; Mechanism; Structure; Inhibitor; VIRUS MESSENGER-RNA; RESPIRATORY SYNCYTIAL VIRUS; VESICULAR STOMATITIS-VIRUS; NONSTRUCTURAL PROTEIN NSP1; DENGUE VIRUS; IN-VITRO; INFLUENZA-VIRUS; MOSAIC-VIRUS; FLAVIVIRUS METHYLTRANSFERASE; PREDOMINANT MECHANISM;
D O I
10.1016/j.antiviral.2012.07.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Most viruses modify their genomic and mRNA 5'-ends with the addition of an RNA cap, allowing efficient mRNA translation, limiting degradation by cellular 5'-3' exonucleases, and avoiding its recognition as foreign RNA by the host cell. Viral RNA caps can be synthesized or acquired through the use of a capping machinery which exhibits a significant diversity in organization, structure and mechanism relative to that of their cellular host. Therefore, viral RNA capping has emerged as an interesting field for antiviral drug design. Here, we review the different pathways and mechanisms used to produce viral mRNA 5'-caps, and present current structures, mechanisms, and inhibitors known to act on viral RNA capping. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:21 / 31
页数:11
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