Department of Physics, Chalmers University of Technology, SE-41296 Göteborg, Sweden.
UniSA: Clinical and Health Sciences, University of South Australia, 5000 Adelaide, Australia.
Nano Lett. 2021 Oct 13;21(19):8503-8509. doi: 10.1021/acs.nanolett.1c02092. Epub 2021 Aug 17.
During diffusion of nanoparticles bound to a cellular membrane by ligand-receptor pairs, the distance to the laterally mobile interface is sufficiently short for their motion to depend not only on the membrane-mediated diffusivity of the tethers but also in a not yet fully understood manner on nanoparticle size and interfacial hydrodynamics. By quantifying diffusivity, velocity, and size of individual membrane-bound liposomes subjected to a hydrodynamic shear flow, we have successfully separated the diffusivity contributions from particle size and number of tethers. The obtained diffusion-size relations for synthetic and extracellular lipid vesicles are not well-described by the conventional no-slip boundary condition, suggesting partial slip as well as a significant diffusivity dependence on the distance to the lipid bilayer. These insights, extending the understanding of diffusion of biological nanoparticles at lipid bilayers, are of relevance for processes such as cellular uptake of viruses and lipid nanoparticles or labeling of cell-membrane-residing molecules.
在配体-受体对结合在细胞膜上的纳米颗粒扩散过程中,到侧向可移动界面的距离足够短,以至于它们的运动不仅取决于膜介导的连接物扩散率,而且还以尚未完全理解的方式取决于纳米颗粒的大小和界面流体动力学。通过量化单个细胞膜结合脂质体在流体剪切流中的扩散率、速度和大小,我们成功地将扩散率的贡献从颗粒大小和连接物数量中分离出来。所获得的合成和细胞外脂质囊泡的扩散-尺寸关系不能很好地用传统的无滑移边界条件来描述,这表明存在部分滑移以及扩散率与脂质双层的距离有显著的依赖性。这些见解扩展了对脂质双层上生物纳米颗粒扩散的理解,对于病毒和脂质纳米颗粒的细胞摄取或细胞膜驻留分子的标记等过程具有重要意义。