Jacobson Kurt H, Gunsolus Ian L, Kuech Thomas R, Troiano Julianne M, Melby Eric S, Lohse Samuel E, Hu Dehong, Chrisler William B, Murphy Catherine J, Orr Galya, Geiger Franz M, Haynes Christy L, Pedersen Joel A
Department of Chemistry, University of Minnesota , Minneapolis, Minnesota 55455, United States.
Department of Chemistry, Northwestern University , Evanston, Illinois 60208, United States.
Environ Sci Technol. 2015 Sep 1;49(17):10642-50. doi: 10.1021/acs.est.5b01841. Epub 2015 Aug 12.
Design of nanomedicines and nanoparticle-based antimicrobial and antifouling formulations and assessment of the potential implications of nanoparticle release into the environment requires understanding nanoparticle interaction with bacterial surfaces. Here we demonstrate the electrostatically driven association of functionalized nanoparticles with lipopolysaccharides of Gram-negative bacterial outer membranes and find that lipopolysaccharide structure influences the extent and location of binding relative to the outer leaflet-solution interface. By manipulating the lipopolysaccharide content in Shewanella oneidensis outer membranes, we observed the electrostatically driven interaction of cationic gold nanoparticles with the lipopolysaccharide-containing leaflet. We probed this interaction by quartz crystal microbalance with dissipation monitoring (QCM-D) and second harmonic generation (SHG) using solid-supported lipopolysaccharide-containing bilayers. The association of cationic nanoparticles increased with lipopolysaccharide content, while no association of anionic nanoparticles was observed. The harmonic-dependence of QCM-D measurements suggested that a population of the cationic nanoparticles was held at a distance from the outer leaflet-solution interface of bilayers containing smooth lipopolysaccharides (those bearing a long O-polysaccharide). Additionally, smooth lipopolysaccharides held the bulk of the associated cationic particles outside of the interfacial zone probed by SHG. Our results demonstrate that positively charged nanoparticles are more likely to interact with Gram-negative bacteria than are negatively charged particles, and this interaction occurs primarily through lipopolysaccharides.
纳米药物以及基于纳米颗粒的抗菌和防污制剂的设计,以及评估纳米颗粒释放到环境中的潜在影响,都需要了解纳米颗粒与细菌表面的相互作用。在此,我们展示了功能化纳米颗粒与革兰氏阴性菌外膜脂多糖的静电驱动结合,并发现脂多糖结构会影响相对于外小叶-溶液界面的结合程度和位置。通过操纵希瓦氏菌外膜中的脂多糖含量,我们观察到阳离子金纳米颗粒与含脂多糖小叶的静电驱动相互作用。我们使用含脂多糖的固体支持双层膜,通过具有耗散监测的石英晶体微天平(QCM-D)和二次谐波产生(SHG)来探测这种相互作用。阳离子纳米颗粒的结合随脂多糖含量增加,而未观察到阴离子纳米颗粒的结合。QCM-D测量的谐波依赖性表明,一部分阳离子纳米颗粒与含有光滑脂多糖(带有长O-多糖的那些)的双层膜的外小叶-溶液界面保持一定距离。此外,光滑脂多糖将大部分相关阳离子颗粒保持在SHG探测的界面区域之外。我们的结果表明,带正电的纳米颗粒比带负电的颗粒更有可能与革兰氏阴性菌相互作用,并且这种相互作用主要通过脂多糖发生。