In vitro transport activity of the fully assembled MexAB-OprM efflux pump from Pseudomonas aeruginosa

被引:38
|
作者
Verchere, Alice [1 ]
Dezi, Manuela [1 ]
Adrien, Vladimir [2 ]
Broutin, Isabelle [1 ]
Picard, Martin [1 ]
机构
[1] Univ Paris 05, CNRS, Fac Pharm Paris, Lab Cristallog & RMN Biol,UMR 8015, F-75006 Paris, France
[2] Univ Paris 06, CNRS, Lab Phys Stat, Ecole Normale Super,UMR 8550, F-75005 Paris, France
来源
NATURE COMMUNICATIONS | 2015年 / 6卷
关键词
MULTIDRUG TRANSPORTER; ESCHERICHIA-COLI; CRYSTAL-STRUCTURE; PROTEIN; RECONSTITUTION; RESISTANCE; PERIPLASM; MECHANISM;
D O I
10.1038/ncomms7890
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Antibiotic resistance is a major public health issue and many bacteria responsible for human infections have now developed a variety of antibiotic resistance mechanisms. For instance, Pseudomonas aeruginosa, a disease-causing Gram-negative bacteria, is now resistant to almost every class of antibiotics. Much of this resistance is attributable to multidrug efflux pumps, which are tripartite membrane protein complexes that span both membranes and actively expel antibiotics. Here we report an in vitro procedure to monitor transport by the tripartite MexAB-OprM pump. By combining proteoliposomes containing the MexAB and OprM portions of the complex, we are able to assay energy-dependent substrate translocation in a system that mimics the dual-membrane architecture of Gram-negative bacteria. This assay facilitates the study of pump transport dynamics and could be used to screen pump inhibitors with potential clinical use in restoring therapeutic activity of old antibiotics.
引用
收藏
页数:6
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