首页> 美国卫生研究院文献>Antimicrobial Agents and Chemotherapy >Functional Linkage between Genes That Regulate Osmotic Stress Responses and Multidrug Resistance Transporters: Challenges and Opportunities for Antibiotic Discovery
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Functional Linkage between Genes That Regulate Osmotic Stress Responses and Multidrug Resistance Transporters: Challenges and Opportunities for Antibiotic Discovery

机译:调节渗透应激反应和多药耐药转运蛋白的基因之间的功能联系:抗生素发现的挑战和机遇。

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摘要

All cells need to protect themselves against the osmotic challenges of their environment by maintaining low permeability to ions across their cell membranes. This is a basic principle of cellular function, which is reflected in the interactions among ion transport and drug efflux genes that have arisen during cellular evolution. Thus, upon exposure to pore-forming antibiotics such as amphotericin B (AmB) or daptomycin (Dap), sensitive cells overexpress common resistance genes to protect themselves from added osmotic challenges. These genes share pathway interactions with the various types of multidrug resistance (MDR) transporter genes, which both preserve the native lipid membrane composition and at the same time eliminate disruptive hydrophobic molecules that partition excessively within the lipid bilayer. An increased understanding of the relationships between the genes (and their products) that regulate osmotic stress responses and MDR transporters will help to identify novel strategies and targets to overcome the current stalemate in drug discovery.
机译:所有细胞都需要通过维持对穿过细胞膜的离子的低渗透性来保护自己免受环境的渗透挑战。这是细胞功能的基本原理,这反映在细胞进化过程中出现的离子转运和药物外排基因之间的相互作用中。因此,在暴露于成孔抗生素(如两性霉素B(AmB)或达托霉素(Dap))后,敏感细胞过表达常见的抗性基因,以保护自己免受额外的渗透挑战。这些基因与各种类型的多药抗性(MDR)转运蛋白基因共享途径相互作用,既保留了天然脂质膜的组成,又消除了在脂质双层中过度分配的破坏性疏水分子。对调节渗透压应激反应的基因(及其产物)与MDR转运蛋白之间关系的进一步了解将有助于确定新的策略和目标,以克服目前药物研发中的僵局。

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