Department of Pharmacology, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.
Microbiol Mol Biol Rev. 2024 Jun 27;88(2):e0019823. doi: 10.1128/mmbr.00198-23. Epub 2024 Mar 29.
SUMMARYInfectious bacteria have both intrinsic and acquired mechanisms to combat harmful biocides that enter the cell. Through adaptive pressures, many of these pathogens have become resistant to many, if not all, of the current antibiotics used today to treat these often deadly infections. One prominent mechanism is the upregulation of efflux systems, especially the resistance-nodulation-cell division class of exporters. These tripartite systems consist of an inner membrane transporter coupled with a periplasmic adaptor protein and an outer membrane channel to efficiently transport a diverse array of substrates from inside the cell to the extracellular space. Detailed mechanistic insight into how these inner membrane transporters recognize and shuttle their substrates can ultimately inform both new antibiotic and efflux pump inhibitor design. This review examines the structural basis of substrate recognition of these pumps and the molecular mechanisms underlying multidrug extrusion, which in turn mediate antimicrobial resistance in bacterial pathogens.
摘要 传染性细菌具有内在和获得性机制来对抗进入细胞的有害消毒剂。由于适应压力,许多病原体对目前用于治疗这些致命感染的许多(如果不是全部)抗生素产生了耐药性。一种突出的机制是外排系统的上调,特别是耐药-结节-细胞分裂(RND)类外排泵。这些三联系统由一个内膜转运蛋白与周质内的一个适配蛋白以及一个外膜通道组成,能够有效地将各种底物从细胞内转运到细胞外。深入了解这些内膜转运蛋白如何识别和转运它们的底物,最终可以为新的抗生素和外排泵抑制剂的设计提供信息。这篇综述考察了这些泵底物识别的结构基础以及多药外排的分子机制,这反过来又介导了细菌病原体的抗药性。
Microbiol Mol Biol Rev. 2024-6-27
Acc Chem Res. 2021-2-16
Microbiology (Reading). 2023-3
Annu Rev Biophys. 2014
Antimicrob Agents Chemother. 2025-4-7
Proc Natl Acad Sci U S A. 2023-7-18
Drug Resist Updat. 2023-1
Proc Natl Acad Sci U S A. 2022-7-26