Bernini Andrea, Spiga Ottavia, Venditti Vincenzo, Prischi Filippo, Bracci Luisa, Huang Jiandong, Tanner Julian A, Niccolai Neri
Biomolecular Structure Research Center, Department of Molecular Biology, University of Siena, I-53100 Siena, Italy.
Biochem Biophys Res Commun. 2006 May 19;343(4):1101-4. doi: 10.1016/j.bbrc.2006.03.069. Epub 2006 Mar 23.
SARS coronavirus, SCV, has been recently responsible of a sudden and widespread infection which caused almost 800 victims. The limited amount of SCV protein structural information is partially responsible of the lack of specific drugs against the virus. Coronavirus helicases are very conserved and peculiar proteins which have been proposed as suitable targets for antiviral drugs, such as bananins, which have been recently shown to inhibit the SCV helicase in vitro. Here, the quaternary structure of SCV helicase has been predicted, which will provide a solid foundation for the rational design of other antiviral helicase inhibitors.
严重急性呼吸综合征冠状病毒(SARS coronavirus,SCV)最近引发了一场突然且广泛传播的感染,导致近800人死亡。SCV蛋白质结构信息有限,这在一定程度上导致了缺乏针对该病毒的特效药物。冠状病毒解旋酶是非常保守且独特的蛋白质,已被提议作为抗病毒药物的合适靶点,比如香蕉素,最近已证明其在体外能抑制SCV解旋酶。在此,已预测出SCV解旋酶的四级结构,这将为合理设计其他抗病毒解旋酶抑制剂提供坚实基础。