Chemical Biology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Department of Chemistry and Biochemistry, University of Oklahoma, Norman, OK, USA.
Nat Chem Biol. 2020 Dec;16(12):1293-1302. doi: 10.1038/s41589-020-00674-6. Epub 2020 Nov 16.
We live in the era of antibiotic resistance, and this problem will progressively worsen if no new solutions emerge. In particular, Gram-negative pathogens present both biological and chemical challenges that hinder the discovery of new antibacterial drugs. First, these bacteria are protected from a variety of structurally diverse drugs by a low-permeability barrier composed of two membranes with distinct permeability properties, in addition to active drug efflux, making this cell envelope impermeable to most compounds. Second, chemical libraries currently used in drug discovery contain few compounds that can penetrate Gram-negative bacteria. As a result of these challenges, intensive screening campaigns have led to few successes, highlighting the need for new approaches to identify regions of chemical space that are specifically relevant to antibacterial drug discovery. Herein we provide an overview of emerging insights into this problem and outline a general approach to addressing it using prospective analysis of chemical libraries for the ability of compounds to accumulate in Gram-negative bacteria. The overall goal is to develop robust cheminformatic tools to predict Gram-negative permeation and efflux, which can then be used to guide medicinal chemistry campaigns and the design of antibacterial discovery libraries.
我们生活在抗生素耐药性的时代,如果没有新的解决方案出现,这个问题将会逐步恶化。特别是革兰氏阴性病原体既具有生物学挑战,也具有化学挑战,这阻碍了新的抗菌药物的发现。首先,这些细菌受到由两层具有不同通透性特性的膜组成的低通透性屏障的保护,除了主动药物外排,使这种细胞膜对大多数化合物都不可渗透。其次,目前用于药物发现的化学文库中只有很少的化合物可以穿透革兰氏阴性菌。由于这些挑战,密集的筛选活动收效甚微,这凸显了需要新的方法来识别与抗菌药物发现特别相关的化学空间区域。本文概述了这一问题的新见解,并概述了一种使用化合物在革兰氏阴性菌中积累能力的化学文库的前瞻性分析来解决这一问题的一般方法。总体目标是开发强大的计算化学工具来预测革兰氏阴性菌的渗透和外排,然后可以将这些工具用于指导药物化学研究和抗菌药物发现文库的设计。