Development and validation of RdRp Screen, a crystallization screen for viral RNA-dependent RNA polymerises

被引:9
作者
Riccio, Federica [1 ]
Talapatra, Sandeep K. [1 ,4 ]
Oxenford, Sally [2 ]
Angell, Richard [2 ]
Mazzon, Michela [3 ]
Kozielski, Frank [1 ]
机构
[1] UCL Sch Pharm, Dept Pharmaceut & Biol Chem, 29-39 Brunswick Sq, London WC1N 1AX, England
[2] UCL Sch Pharm, Translat Res Off, 29-39 Brunswick Sq, London WC1N 1AX, England
[3] UCL MRC Lab Mol Cell Biol, Gower St, London WC1E 6BT, England
[4] AstraZeneca, Discovery Biol, Discovery Sci, IMED Biotech Unit, Alderley Pk, Macclesfield, Cheshire, England
来源
BIOLOGY OPEN | 2019年 / 8卷 / 01期
关键词
Dengue virus; Crystallization screen; RNA-dependent RNA polymerase; Flavivirus; Antiviral drug discovery; CRYSTAL-STRUCTURE; VIRUS; NS5; SOFOSBUVIR/VELPATASVIR; DOMAIN; TARGET;
D O I
10.1242/bio.037663
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Members of the Flaviviridae family constitute a severe risk to human health. Whilst effective drugs have been developed against the hepacivirus HCV, no antiviral therapy is currently available for any other viruses, induding the flaviviruses dengue (DENV), West Nile and Zika viruses. The RNA-dependent RNA polymerase (RdRp) is responsible for viral replication and represents an excellent therapeutic target with no homologue found in mammals. The identification of compounds targeting the RdRp of other flaviviruses is an active area of research. One of the main factors hampering further developments in the field is the difficulty in obtaining high-quality crystal information that could aid a structure-based drug discovery approach. To address this, we have developed a convenient and economical 96-well screening platform. We validated the screen by successfully obtaining crystals of both native DENV serotype 2 and 3 RdRps under several conditions included in the screen. In addition, we have obtained crystal structures of RdRp3 in complex with a previously identified fragment using both soaking and co-crystallization techniques. This work will streamline and accelerate the generation of crystal structures of viral RdRps and provide the community with a valuable tool to aid the development of structure-based antiviral design.
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页数:10
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