Emerging antiviral targets for influenza A virus

被引:86
作者
Krug, Robert M. [1 ]
Aramini, James M. [2 ]
机构
[1] Univ Texas Austin, Inst Cellular & Mol Biol, Sect Mol Genet & Microbiol, Austin, TX 78712 USA
[2] Rutgers State Univ, Dept Mol Biol & Biochem, Ctr Adv Biotechnol & Med, Piscataway, NJ 08854 USA
基金
美国国家卫生研究院;
关键词
DOUBLE-STRANDED-RNA; PRE-MESSENGER-RNAS; NS1; PROTEIN; STRUCTURAL BASIS; H5N1; VIRUS; CRYSTAL-STRUCTURE; EFFECTOR DOMAIN; NONSTRUCTURAL PROTEIN-1; CONFORMATIONAL-CHANGE; PANDEMIC INFLUENZA;
D O I
10.1016/j.tips.2009.03.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The potential threat of a pandemic caused by H5N1 influenza A viruses has stimulated increased research on developing new antivirals against influenza A viruses. Current antivirals are directed against the M2 protein (named adamantanes) and the neuraminidase (named zanamivir and oseltamivir). However, both seasonal and H5N1 influenza A viruses have developed resistance to adamantanes and oseltamivir. Accordingly, new antivirals directed at the M2 and neuraminidase proteins, and against the hemagglutinin protein, are being developed. In addition, elucidation of the structural basis for several crucial functions of other viral proteins (specifically the non-structural NS1A protein, the nucleoprotein and the viral polymerase) has identified novel targets for the development of new antivirals. Here, we describe how functional and structural studies led to the discovery of these novel targets and also how structural information is facilitating the rational design of new drugs against previously identified targets.
引用
收藏
页码:269 / 277
页数:9
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