Clifton Luke A, Holt Stephen A, Hughes Arwel V, Daulton Emma L, Arunmanee Wanatchaporn, Heinrich Frank, Khalid Syma, Jefferies Damien, Charlton Timothy R, Webster John R P, Kinane Christian J, Lakey Jeremy H
ISIS Pulsed Neutron and Muon Source, Science and Technology Facilities Council, Rutherford Appleton Laboratory, Harwell Oxford Campus, Didcot, Oxfordshire, OX11 OQX (UK).
Bragg Institute, Australian Nuclear Science and Technology Organisation, Locked Bag 2001, Kirrawee DC, NSW 2232 (Australia).
Angew Chem Int Ed Engl. 2015 Oct 5;54(41):11952-5. doi: 10.1002/anie.201504287. Epub 2015 Sep 1.
Gram-negative bacteria are an increasingly serious source of antibiotic-resistant infections, partly owing to their characteristic protective envelope. This complex, 20 nm thick barrier includes a highly impermeable, asymmetric bilayer outer membrane (OM), which plays a pivotal role in resisting antibacterial chemotherapy. Nevertheless, the OM molecular structure and its dynamics are poorly understood because the structure is difficult to recreate or study in vitro. The successful formation and characterization of a fully asymmetric model envelope using Langmuir-Blodgett and Langmuir-Schaefer methods is now reported. Neutron reflectivity and isotopic labeling confirmed the expected structure and asymmetry and showed that experiments with antibacterial proteins reproduced published in vivo behavior. By closely recreating natural OM behavior, this model provides a much needed robust system for antibiotic development.
革兰氏阴性菌是抗生素耐药性感染日益严重的来源,部分原因在于其具有特征性的保护性包膜。这种复杂的、厚20纳米的屏障包括一层高度不可渗透的不对称双层外膜(OM),它在抵抗抗菌化疗中起关键作用。然而,由于该结构难以在体外重建或研究,人们对其分子结构及其动力学了解甚少。现在报告了使用朗缪尔-布洛杰特和朗缪尔-谢弗方法成功形成并表征了一个完全不对称的模型包膜。中子反射率和同位素标记证实了预期的结构和不对称性,并表明使用抗菌蛋白进行的实验重现了已发表的体内行为。通过紧密重现天然外膜的行为,该模型为抗生素开发提供了一个急需的强大系统。