Nuclear trafficking of proteins from RNA viruses: Potential target for antivirals?

被引:83
作者
Caly, Leon [1 ]
Wagstaff, Kylie M. [1 ]
Jans, David A. [1 ]
机构
[1] Monash Univ, Dept Biochem & Mol Biol, Clayton, Vic 3800, Australia
关键词
Nuclear transport; HIV integrase; Influenza A NP; Dengue virus NS5; Respiratory syncytial virus matrix; Rift valley fever virus NSs; Venezuelan equine encephalitis virus; Ivermectin; VIRAL MATRIX PROTEIN; FEVER VIRUS; LOCALIZATION SIGNAL; INFECTED-CELLS; HIV-1; INTEGRASE; NONDIVIDING CELLS; TYPE-1; INFLUENZA-VIRUS; POLYMERASE NS5; HOST-CELLS;
D O I
10.1016/j.antiviral.2012.06.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A key aspect of the infectious cycle of many viruses is the transport of specific viral proteins into the host cell nucleus to perturb the antiviral response. Examples include a number of RNA viruses that are significant human pathogens, such as human immunodeficiency virus (HIV)-1, influenza A, dengue, respiratory syncytial virus and rabies, as well agents that predominantly infect livestock, such as Rift valley fever virus and Venezuelan equine encephalitis virus. Inhibiting the nuclear trafficking of viral proteins as a therapeutic strategy offers an attractive possibility, with important recent progress having been made with respect to HIV-1 and dengue. The results validate nuclear protein import as an antiviral target, and suggest the identification and development of nuclear transport inhibitors as a viable therapeutic approach for a range of human and zoonotic pathogenic viruses. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:202 / 206
页数:5
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