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一种用于鉴定Lol(脂蛋白定位)系统抑制剂的新型筛选方法,Lol系统是一种新型抗菌靶点。

A new screening method to identify inhibitors of the Lol (localization of lipoproteins) system, a novel antibacterial target.

作者信息

Ito Hideaki, Ura Atsushi, Oyamada Yoshihiro, Yoshida Hiroaki, Yamagishi Jun-Ichi, Narita Shin-Ichiro, Matsuyama Shin-Ichi, Tokuda Hajime

机构信息

Pharmacology Research Laboratories, Dainippon Sumitomo Pharma Co Ltd, Suita, Osaka, Japan.

出版信息

Microbiol Immunol. 2007;51(3):263-70. doi: 10.1111/j.1348-0421.2007.tb03906.x.

Abstract

As the Lol system, which is involved in localization of lipoproteins, is essential for Escherichia coli growth and widely conserved among gram-negative bacteria, it is considered to be a promising target for the development of anti-gram-negative bacterial agents. However, no high-throughput screening method has so far been developed to screen for Lol system inhibitors. By combining three assay systems (anucleate cell blue assay, Lpp assay, and LolA-dependent release inhibition assay) and a drug susceptibility test, we have successfully developed a new screening method for identification of compounds that inhibit the Lol system. Using this new screening method, we screened 23,600 in-house chemical compounds and found 2 Lol system inhibitors. We therefore conclude that our new screening method can efficiently identify new antibacterial agents that target the Lol system.

摘要

由于参与脂蛋白定位的Lol系统对大肠杆菌的生长至关重要,且在革兰氏阴性菌中广泛保守,因此它被认为是开发抗革兰氏阴性菌药物的一个有前景的靶点。然而,迄今为止尚未开发出高通量筛选方法来筛选Lol系统抑制剂。通过结合三种检测系统(无核细胞蓝色检测、Lpp检测和LolA依赖性释放抑制检测)以及药敏试验,我们成功开发了一种新的筛选方法,用于鉴定抑制Lol系统的化合物。使用这种新的筛选方法,我们筛选了23600种内部化合物,发现了2种Lol系统抑制剂。因此,我们得出结论,我们的新筛选方法可以有效地鉴定针对Lol系统的新型抗菌剂。

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