Inhibition of self-splicing group I intron RNA: High-throughput screening assays

被引:17
作者
Mei, HY [1 ]
Cui, M [1 ]
Sutton, ST [1 ]
Truong, HN [1 ]
Chung, FZ [1 ]
Czarnik, AW [1 ]
机构
[1] WARNER LAMBERT PARKE DAVIS,PARKE DAVIS PHARMACEUT RES DIV,DEPT THERAPEUT,ANN ARBOR,MI 48106
关键词
D O I
10.1093/nar/24.24.5051
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
High-throughput screening assays have been developed to rapidly identify small molecule inhibitors targeting catalytic group I introns, Biochemical reactions catalyzed by a self-splicing group I intron derived from Pneumocystis carinii or from bacteriophage T4 have been investigated, In vitro biochemical assays amenable to high-throughput screening have been established, Small molecules that inhibit the functions of group I introns have been identified, These inhibitors should be useful in better understanding ribozyme catalysis or in therapeutic intervention of group I intron-containing microorganisms.
引用
收藏
页码:5051 / 5053
页数:3
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