4.7 Review

The viral RNA capping machinery as a target for antiviral drugs

期刊

ANTIVIRAL RESEARCH
卷 96, 期 1, 页码 21-31

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.antiviral.2012.07.007

关键词

5 '-Triphosphatase; Guanylyltransferase; Methyltransferase; Endonuclease; Cap snatching; Mechanism; Structure; Inhibitor

资金

  1. Fondation pour la Recherche Medicale
  2. Direction Generale de l'Armement [07co404]
  3. Infectiopole-Sud
  4. European Union [260644]

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据