High-throughput screening for a SARS-CoV-2 frameshifting inhibitor using a cell-free protein synthesis system

被引:0
|
作者
Machida, Kodai [1 ]
Tanaka, Rin [1 ]
Miki, Seraya [1 ]
Noseda, Shotaro [1 ]
Yuasa-Sunagawa, Mayumi [1 ]
Imataka, Hiroaki [1 ]
机构
[1] Univ Hyogo, Grad Sch Engn, Dept Appl Chem, Himeji 6712201, Japan
关键词
cell-free protein synthesis; drug discovery; programmed-1 ribosomal frameshifting; SARS-CoV-2; screening; SARS-CORONAVIRUS; LIGAND; IDENTIFICATION; AGGREGATION;
D O I
10.2144/btn-2023-0102
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Programmed-1 ribosomal frameshifting (-1 PRF) is a translational mechanism adopted by some viruses, including SARS-CoV-2. To find a compound that can inhibit -1 PRF in SARS-CoV-2, we set up a high-throughput screening system using a HeLa cell extract-derived cell-free protein synthesis (CFPS) system. A total of 32,000 compounds were individually incubated with the CFPS system programmed with a -1 PRF-EGFP template. Several compounds were observed to decrease the -1 PRF-driven fluorescence, and one of them had some suppressive effect on -1 PRF of a SARS-CoV-2 genome sequence in transfected cells. Thus the CFPS system can be used as a tool for a high-throughput screening of chemicals.
引用
收藏
页码:161 / 168
页数:8
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