Vaccinia Virus Virulence Factor N1L is a Novel Promising Target for Antiviral Therapeutic Intervention

被引:107
作者
Cheltsov, Anton V. [1 ,2 ]
Aoyagi, Mika [1 ]
Aleshin, Alexander [1 ]
Yu, Eric Chi-Wang [1 ]
Gilliland, Taylor [1 ]
Zhai, Dayong [1 ]
Bobkov, Andrey A. [1 ]
Reed, John C. [1 ]
Liddington, Robert C. [1 ]
Abagyan, Ruben [2 ]
机构
[1] Burnham Inst Med Res, Infect & Inflammatory Dis Ctr, La Jolla, CA 92037 USA
[2] Univ Calif San Diego, La Jolla, CA 92093 USA
关键词
ENERGY LANDSCAPE PERSPECTIVE; LIGAND DOCKING; MOLECULAR DOCKING; FOLDING FUNNELS; NATIVE-STATE; MONTE-CARLO; PROTEIN; BCL-2; BINDING; RESVERATROL;
D O I
10.1021/jm901446n
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The 14 kDa homodimeric N1L protein is a potent vaccinia and variola (smallpox) virulence factor. It is not essential for viral replication, but it causes a strong attenuation of viral production in culture when deleted. The N1L protein is predicted to contain the BH3-like binding domain characteristic of Bcl-2 family proteins, and it is able to bind the BH3 peptides. Its overexpression has been reported to prevent infected cells from committing apoptosis. Therefore, interfering with the N1L apoptotic blockade may be a legitimate therapeutic strategy affecting the viral growth. By using in silico ligand docking and an array of in vitro assays, we have identified submicromolar (600 nM) N1L antagonists belonging to the family of polyphenols. Their affinity is comparable to that of the BH3 peptides (70-1000 nM). We have also identified the natural polyphenol resveratrol as a moderate N1L inhibitor. Finally, we show that our ligands efficiently inhibit growth of vaccinia virus.
引用
收藏
页码:3899 / 3906
页数:8
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