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环二核苷酸(c-di-GMP、c-di-AMP和cGAMP)信号传导已发展到可以被小分子抑制的阶段。

Cyclic dinucleotide (c-di-GMP, c-di-AMP, and cGAMP) signalings have come of age to be inhibited by small molecules.

作者信息

Opoku-Temeng Clement, Zhou Jie, Zheng Yue, Su Jianmei, Sintim Herman O

机构信息

Department of Chemistry, Center for Drug Discovery, Purdue University, West Lafayette, IN 47907, USA.

出版信息

Chem Commun (Camb). 2016 Aug 4;52(60):9327-42. doi: 10.1039/c6cc03439j. Epub 2016 Jun 24.

Abstract

Bacteria utilize nucleotide-based second messengers to regulate a myriad of physiological processes. Cyclic dinucleotides have emerged as central regulators of bacterial physiology, controlling processes ranging from cell wall homeostasis to virulence production, and so far over thousands of manuscripts have provided biological insights into c-di-NMP signaling. The development of small molecule inhibitors of c-di-NMP signaling has significantly lagged behind. Recent developments in assays that allow for high-throughput screening of inhibitors suggest that the time is right for a concerted effort to identify inhibitors of these fascinating second messengers. Herein, we review c-di-NMP signaling and small molecules that have been developed to inhibit cyclic dinucleotide-related enzymes.

摘要

细菌利用基于核苷酸的第二信使来调节众多生理过程。环二核苷酸已成为细菌生理学的核心调节因子,控制着从细胞壁稳态到毒力产生等一系列过程,到目前为止,已有数千篇手稿提供了关于环二鸟苷酸信号传导的生物学见解。环二核苷酸信号传导的小分子抑制剂的开发明显滞后。能够进行抑制剂高通量筛选的检测方法的最新进展表明,现在是齐心协力鉴定这些迷人的第二信使抑制剂的时候了。在此,我们综述环二核苷酸信号传导以及为抑制环二核苷酸相关酶而开发的小分子。

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