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合理设计的折叠体佐剂可增强抗生素疗效,促进膜超极化。

Rationally designed foldameric adjuvants enhance antibiotic efficacy promoting membrane hyperpolarization.

作者信息

Bhaumik Kaushik Nath, Hetényi Anasztázia, Olajos Gábor, Martins Ana, Spohn Réka, Németh Lukács, Jojart Balázs, Szili Petra, Dunai Anett, Jangir Pramod K, Daruka Lejla, Földesi Imre, Kata Diána, Pál Csaba, Martinek Tamás A

机构信息

Department of Medical Chemistry, University of Szeged Dóm tér 8 Szeged HU-6720 Hungary

Synthetic and Systems Biology Unit, Biological Research Centre, Eötvös Loránd Research Network (ELKH) Szeged Hungary.

出版信息

Mol Syst Des Eng. 2021 Nov 11;7(1):21-33. doi: 10.1039/d1me00118c. eCollection 2022 Jan 4.

Abstract

The negative membrane potential of bacterial cells influences crucial cellular processes. Inspired by the molecular scaffold of the antimicrobial peptide PGLa, we have developed antimicrobial foldamers with a computer-guided design strategy. The novel PGLa analogues induce sustained membrane hyperpolarization. When co-administered as an adjuvant, the resulting compounds - PGLb1 and PGLb2 - have substantially reduced the level of antibiotic resistance of multi-drug resistant , and clinical isolates. The observed antibiotic potentiation was mediated by hyperpolarization of the bacterial membrane caused by the alteration of cellular ion transport. Specifically, PGLb1 and PGLb2 are selective ionophores that enhance the Goldman-Hodgkin-Katz potential across the bacterial membrane. These findings indicate that manipulating bacterial membrane electrophysiology could be a valuable tool to overcome antimicrobial resistance.

摘要

细菌细胞的负膜电位影响着关键的细胞过程。受抗菌肽PGLa分子支架的启发,我们采用计算机辅助设计策略开发了抗菌折叠体。新型PGLa类似物可诱导持续的膜超极化。当作为佐剂共同给药时,所得化合物——PGLb1和PGLb2——已大幅降低了多药耐药临床分离株的抗生素耐药水平。观察到的抗生素增效作用是由细胞离子转运改变导致的细菌膜超极化介导的。具体而言,PGLb1和PGLb2是选择性离子载体,可增强细菌膜上的戈德曼-霍奇金- Katz电位。这些发现表明,操纵细菌膜电生理学可能是克服抗菌耐药性的一种有价值的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e63/8724909/77668482265a/d1me00118c-f1.jpg

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