Discovery of Novel Antimicrobial Agents Targeting the Bacterial RNA Polymerase by High-Throughput Virtual Screening

IF 0.4 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
K. Onodera, T. Kawasaki, S. Kamijo
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引用次数: 1

Abstract

Bacterial RNA polymerase (RNAP) is the least popular target for antibiotics, and currently Rifampicin is only an approved drug for clinical use. However, RNAP is essential for bacterial growth and survival, and it can be a promising target for antimicrobial agents. Thus, we decided to search new antimicrobial agents for RNAP by virtual screening. When virtual screenings are performed, certain compounds repeatedly appears on hits covering a wide range of targets (frequently hitters). Also, the performance of hit generation is important factor in success of the virtual screening. Since we previously developed the optimized docking scores, we examined our scoring methods with rigorous removals of frequent hitters. We used two complex structures for RNAP, and also used two unrelated structures as negative controls to remove frequent hitters. Finally, we selected seven high-scored candidates from hits, and two of them showed the inhibition of Gram-positive bacteria by paper disk agar diffusion assay in vivo.
利用高通量虚拟筛选技术发现靶向细菌RNA聚合酶的新型抗菌药物
细菌RNA聚合酶(RNAP)是最不受欢迎的抗生素靶点,目前利福平仅被批准用于临床。然而,RNAP对细菌的生长和生存至关重要,它可以成为抗微生物药物的一个有希望的靶点。因此,我们决定通过虚拟筛选来寻找新的抗RNAP药物。当执行虚拟筛选时,某些化合物反复出现在覆盖大范围目标的命中(通常是命中)。同时,命中生成的性能也是虚拟筛选成功的重要因素。因为我们之前开发了优化的对接得分,所以我们检查了我们的得分方法,严格删除了频繁击球者。我们使用了两个复杂的RNAP结构,并使用了两个不相关的结构作为阴性对照,以去除频繁的撞击。最后,我们从命中选择了7个得分较高的候选物,其中2个通过纸盘琼脂扩散实验在体内表现出对革兰氏阳性菌的抑制作用。
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来源期刊
Chem-Bio Informatics Journal
Chem-Bio Informatics Journal BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
0.60
自引率
0.00%
发文量
8
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