Development and validation of a high-throughput screen for inhibitors of SARS CoV and its application in screening of a 100,000-compound library

被引:62
|
作者
Severson, William E.
Shindo, Nice
Sosa, Mindy
Fletcher, Thomas, III
White, E. Lucile
Ananthan, Subramaniam
Jonsson, Colleen B.
机构
[1] So Res Inst, Dept Biochem & Mol Biol, Birmingham, AL 35205 USA
[2] So Res Inst, Dept Chem, Birmingham, AL 35205 USA
[3] So Res Inst, High Throughput Screening Ctr, Birmingham, AL 35205 USA
关键词
high-throughput screening; severe acute respiratory syndrome; coronavirus; cytopathic effect;
D O I
10.1177/1087057106296688
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The authors have developed a high-throughput screen (HTS) that allows for the identification of potential inhibitors of the severe acute respiratory syndrome coronavirus (SARS CoV) from large compound libraries. The luminescent-based assay measures the inhibition of SARS CoV-induced cytopathic effect (CPE) in Vero E6 cells. The assay was validated in 96-well plates in a BSL3 containment facility. The assay is sensitive and robust, with Z values > 0.6, signal to background (S/B) > 16, and signal to noise (S/N) > 3. The assay was further validated with 2 different diversity sets of compounds against the SARS CoV The "hit" rate for both libraries was approximately 0.01%. The validated HTS assay was then employed to screen a 100,000 compound library against SARS CoV. The hit rate for the library in a single-dose format was determined to be approximately 0.8%. Screening of the 3 libraries resulted in the identification of several novel compounds that effectively inhibited the CPE of SARS CoV in vitro-compounds which will serve as excellent lead candidates for further evaluation. At a 10-mu M concentration, 3 compounds with selective indexes (SI50) of > 53 were discovered.
引用
收藏
页码:33 / 40
页数:8
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