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抗击抗微生物药物耐药性:通过监督分子动力学(SuMD)和分子对接模拟研究 NorA 外排泵识别 2-苯基喹啉抑制剂的见解。

Fighting Antimicrobial Resistance: Insights on How the NorA Efflux Pump Recognizes 2-Phenylquinoline Inhibitors by Supervised Molecular Dynamics (SuMD) and Molecular Docking Simulations.

机构信息

Department of Pharmaceutical Sciences, Department of Excellence 2018-2022, University of Perugia, Via del Liceo, 1, 06123 Perugia, Italy.

Molecular Modeling Section (MMS), Department of Pharmaceutical and Pharmacological Sciences, University of Padova, via Marzolo 5, 35131 Padova, Italy.

出版信息

J Chem Inf Model. 2023 Aug 14;63(15):4875-4887. doi: 10.1021/acs.jcim.3c00516. Epub 2023 Jul 29.

DOI:10.1021/acs.jcim.3c00516
Abstract

The superbug () exhibits several resistance mechanisms, including efflux pumps, that strongly contribute to antimicrobial resistance. In particular, the NorA efflux pump activity is associated with resistance to fluoroquinolone antibiotics (., ciprofloxacin) by promoting their active extrusion from cells. Thus, since efflux pump inhibitors (EPIs) are able to increase antibiotic concentrations in bacteria as well as restore their susceptibility to these agents, they represent a promising strategy to counteract bacterial resistance. Additionally, the very recent release of two NorA efflux pump cryo-electron microscopy (cryo-EM) structures in complex with synthetic antigen-binding fragments (Fabs) represents a real breakthrough in the study of antibiotic resistance. In this scenario, supervised molecular dynamics (SuMD) and molecular docking experiments were combined to investigate for the first time the molecular mechanisms driving the interaction between NorA and efflux pump inhibitors (EPIs), with the ultimate goal of elucidating how the NorA efflux pump recognizes its inhibitors. The findings provide insights into the dynamic NorA-EPI intermolecular interactions and lay the groundwork for future drug discovery efforts aimed at the identification of novel molecules to fight antimicrobial resistance.

摘要

超级细菌()表现出多种耐药机制,包括外排泵,这强烈促成了抗微生物药物的耐药性。特别是,NorA 外排泵的活性与对氟喹诺酮类抗生素(例如环丙沙星)的耐药性有关,它通过促进这些抗生素从细胞中主动外排来发挥作用。因此,由于外排泵抑制剂(EPIs)能够增加细菌内抗生素的浓度并恢复它们对这些药物的敏感性,因此它们代表了对抗细菌耐药性的一种有前途的策略。此外,最近发布的两个与合成抗原结合片段(Fabs)结合的 NorA 外排泵冷冻电子显微镜(cryo-EM)结构,在研究抗生素耐药性方面取得了真正的突破。在此背景下,首次将有监督的分子动力学(SuMD)和分子对接实验相结合,研究了 NorA 与外排泵抑制剂(EPIs)之间相互作用的分子机制,最终目标是阐明 NorA 外排泵如何识别其抑制剂。这些发现提供了对动态 NorA-EPI 分子间相互作用的深入了解,并为未来旨在识别新型分子以对抗抗微生物药物耐药性的药物发现工作奠定了基础。

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