Laboratoire de Cristallographie et RMN Biologiques, UMR 8015, CNRS, Université Paris Descartes, Faculté de Pharmacie de Paris, 4 Avenue de l'Observatoire, 75006 Paris, France.
Laboratoire de physique statistique de l'École Normale Supérieure, UMR 8550, CNRS, Université Pierre et Marie Curie, 24 rue Lhomond, 75005 Paris, France.
Nat Commun. 2015 Apr 22;6:6890. doi: 10.1038/ncomms7890.
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.
抗生素耐药性是一个主要的公共卫生问题,许多导致人类感染的细菌现在已经发展出多种抗生素耐药机制。例如,铜绿假单胞菌,一种引起疾病的革兰氏阴性菌,现在几乎对每一类抗生素都有耐药性。这种耐药性很大程度上归因于多药外排泵,它是一种三联膜蛋白复合物,横跨两个膜并主动排出抗生素。在这里,我们报告了一种体外程序来监测三联 MexAB-OprM 泵的运输。通过将含有该复合物的 MexAB 和 OprM 部分的蛋白脂质体结合起来,我们能够在模拟革兰氏阴性菌双膜结构的系统中检测到能量依赖性底物易位。该测定法有助于研究泵转运动力学,并且可用于筛选具有潜在临床应用的泵抑制剂,以恢复旧抗生素的治疗活性。