Structural understanding of efflux-mediated drug resistance: potential routes to efflux inhibition

被引:31
作者
McKeegan, KS [1 ]
Borges-Walmsley, MI [1 ]
Walmsey, AR [1 ]
机构
[1] Univ Durham, Wolfson Res Inst, Ctr Infect Dis, Dept Biol Sci, Stockton On Tees TS17 6BH, England
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
D O I
10.1016/j.coph.2004.07.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The active efflux of cytotoxic drugs mediated by multidrug transporters is the basis of multidrug resistance in prokaryotic and eukaryotic cells. Individual multidrug transporters can be extremely versatile, often exhibiting a staggering range of substrate specificity that can negate the effects of clinically relevant therapies. The effective treatment of bacterial, fungal and protozoan infections, along with certain cancer treatments, has been compromised by the presence of multidrug transporters. Traditionally, advances in the understanding of multidrug transporters have been made through biochemical analyses; more recently, however, fundamental advances have been made with the elucidation of several three dimensional structures of representative multidrug pumps. Biochemical and structural analysis of multidrug pumps could lead to the development of novel 'anti-efflux' therapies.
引用
收藏
页码:479 / 486
页数:8
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