Proton-dependent multidrug efflux systems.

I T Paulsen, M H Brown, R A Skurray
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引用次数: 253

Abstract

Multidrug efflux systems display the ability to transport a variety of structurally unrelated drugs from a cell and consequently are capable of conferring resistance to a diverse range of chemotherapeutic agents. This review examines multidrug efflux systems which use the proton motive force to drive drug transport. These proteins are likely to operate as multidrug/proton antiporters and have been identified in both prokaryotes and eukaryotes. Such proton-dependent multidrug efflux proteins belong to three distinct families or superfamilies of transport proteins: the major facilitator superfamily (MFS), the small multidrug resistance (SMR) family, and the resistance/ nodulation/cell division (RND) family. The MFS consists of symporters, antiporters, and uniporters with either 12 or 14 transmembrane-spanning segments (TMS), and we show that within the MFS, three separate families include various multidrug/proton antiport proteins. The SMR family consists of proteins with four TMS, and the multidrug efflux proteins within this family are the smallest known secondary transporters. The RND family consists of 12-TMS transport proteins and includes a number of multidrug efflux proteins with particularly broad substrate specificity. In gram-negative bacteria, some multidrug efflux systems require two auxiliary constituents, which might enable drug transport to occur across both membranes of the cell envelope. These auxiliary constituents belong to the membrane fusion protein and the outer membrane factor families, respectively. This review examines in detail each of the characterized proton-linked multidrug efflux systems. The molecular basis of the broad substrate specificity of these transporters is discussed. The surprisingly wide distribution of multidrug efflux systems and their multiplicity in single organisms, with Escherichia coli, for instance, possessing at least nine proton-dependent multidrug efflux systems with overlapping specificities, is examined. We also discuss whether the normal physiological role of the multidrug efflux systems is to protect the cell from toxic compounds or whether they fulfil primary functions unrelated to drug resistance and only efflux multiple drugs fortuitously or opportunistically.

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依赖质子的多药物外排系统。
多药外排系统显示出从细胞中转运多种结构不相关的药物的能力,因此能够对多种化疗药物产生耐药性。本文综述了利用质子动力驱动药物转运的多药外排系统。这些蛋白可能作为多药物/质子反转运蛋白起作用,并已在原核生物和真核生物中发现。这种质子依赖的多药外排蛋白属于三个不同的转运蛋白家族或超家族:主要促进剂超家族(MFS)、小多药耐药家族(SMR)和耐药/结瘤/细胞分裂家族(RND)。MFS由正转运蛋白、反转运蛋白和单转运蛋白组成,它们具有12或14个跨膜片段(TMS),我们发现在MFS中,三个独立的家族包括各种多药物/质子反转运蛋白。SMR家族由具有4个TMS的蛋白质组成,该家族中的多药物外排蛋白是已知最小的二级转运蛋白。RND家族由12种tms转运蛋白组成,包括许多具有特别广泛底物特异性的多药外排蛋白。在革兰氏阴性菌中,一些多药物外排系统需要两种辅助成分,这可能使药物运输发生在细胞膜的两层。这些辅助成分分别属于膜融合蛋白和外膜因子家族。这篇综述详细检查了每一个特征质子连接的多药物外排系统。讨论了这些转运体广泛的底物特异性的分子基础。多药物外排系统的广泛分布及其在单一生物中的多样性,例如大肠杆菌,具有至少9个具有重叠特异性的质子依赖性多药物外排系统。我们还讨论了多药外排系统的正常生理作用是保护细胞免受有毒化合物的侵害,还是它们履行与耐药性无关的主要功能,只是偶然或机会地外排多种药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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Proton-dependent multidrug efflux systems. Soil microorganisms as controllers of atmospheric trace gases (H2, CO, CH4, OCS, N2O, and NO). The secretory pathway of protists: spatial and functional organization and evolution. T helper cell activation and human retroviral pathogenesis. Flow cytometry and cell sorting of heterogeneous microbial populations: the importance of single-cell analyses.
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