Max Planck Institute for the Science of Light and Friedrich Alexander University, 91058 Erlangen, Germany.
J Phys Chem B. 2014 Feb 13;118(6):1545-54. doi: 10.1021/jp412203t. Epub 2014 Jan 30.
Supported lipid bilayers have been studied intensively over the past two decades. In this work, we study the diffusion of single gold nanoparticles (GNPs) with diameter of 20 nm attached to GM1 ganglioside or DOPE lipids at different concentrations in supported DOPC bilayers. The indefinite photostability of GNPs combined with the high sensitivity of interferometric scattering microscopy (iSCAT) allows us to achieve 1.9 nm spatial precision at 1 ms temporal resolution, while maintaining long recording times. Our trajectories visualize strong transient confinements within domains as small as 20 nm, and the statistical analysis of the data reveals multiple mobilities and deviations from normal diffusion. We present a detailed analysis of our findings and provide interpretations regarding the effect of the supporting substrate and GM1 clustering. We also comment on the use of high-speed iSCAT for investigating diffusion of lipids, proteins, or viruses in lipid membranes with unprecedented spatial and temporal resolution.
在过去的二十年中,人们对支持脂质双层进行了深入研究。在这项工作中,我们研究了直径为 20nm 的金纳米颗粒(GNPs)在不同浓度的 GM1 神经节苷脂或 DOPE 脂质附着在支持的 DOPC 双层膜中的扩散。GNPs 的无限光稳定性结合干涉散射显微镜(iSCAT)的高灵敏度,使我们能够在 1ms 的时间分辨率下达到 1.9nm 的空间精度,同时保持长时间的记录。我们的轨迹可视化了在小至 20nm 的区域内的强烈瞬态限制,并且对数据的统计分析揭示了多种迁移率和偏离正常扩散的情况。我们对研究结果进行了详细的分析,并对支撑基底和 GM1 聚集的影响提供了解释。我们还评论了使用高速 iSCAT 以空前的时空分辨率研究脂质、蛋白质或病毒在脂质膜中的扩散的应用。