Department of Chemistry, University of Florence and CSGI, Florence, Italy.
ISMN-CNR and CSGI, Bologna, Italy.
Phys Chem Chem Phys. 2022 Feb 2;24(5):2762-2776. doi: 10.1039/d1cp03201a.
The bioactivity, biological fate and cytotoxicity of nanomaterials when they come into contact with living organisms are determined by their interaction with biomacromolecules and biological barriers. In this context, the role of symmetry/shape anisotropy of both the nanomaterials and biological interfaces in their mutual interaction, is a relatively unaddressed issue. Here, we study the interaction of gold nanoparticles (NPs) of different shapes (nanospheres and nanorods) with biomimetic membranes of different morphology, flat membranes (2D symmetry, representative of the most common plasma membrane geometry), and cubic membranes (3D symmetry, representative of non-lamellar membranes, found in Nature under certain biological conditions). For this purpose we used an ensemble of complementary structural techniques, including Neutron Reflectometry, Grazing Incidence Small-Angle Neutron Scattering, on a nanometer lengthscale and Confocal Laser Scanning Microscopy on a micrometer length scale. We found that the structural stability of the membrane towards NPs is dependent on the topological characteristic of the lipid assembly and of the NPs, where a higher symmetry gave higher stability. In addition, Confocal Laser Scanning Microscopy analyses highlighted that NPs interact with cubic and lamellar phases according to two distinct mechanisms, related to the different structures of the lipid assemblies. This study for the first time systematically addresses the role of NPs shape in the interaction with lipid assemblies with different symmetry. The results will contribute to improve the fundamental knowledge on lipid interfaces and will provide new insights on the biological function of phase transitions as a response strategy to the exposure of NPs.
当纳米材料与生物体接触时,其生物活性、生物命运和细胞毒性取决于它们与生物大分子和生物屏障的相互作用。在这种情况下,纳米材料和生物界面的对称性/形状各向异性在它们的相互作用中的作用是一个相对未被解决的问题。在这里,我们研究了不同形状(纳米球和纳米棒)的金纳米颗粒(NPs)与不同形态的仿生膜(二维对称,代表最常见的质膜几何形状)和立方膜(三维对称,代表非层状膜,在某些生物条件下在自然界中发现)的相互作用。为此,我们使用了一系列互补的结构技术,包括中子反射率、掠入射小角中子散射,在纳米尺度上和共焦激光扫描显微镜,在微米尺度上。我们发现,膜对 NPs 的结构稳定性取决于脂质组装和 NPs 的拓扑特征,其中更高的对称性赋予更高的稳定性。此外,共焦激光扫描显微镜分析突出表明,NPs 根据两种不同的机制与立方相和层状相相互作用,这与脂质组装的不同结构有关。这项研究首次系统地研究了 NPs 形状在与具有不同对称性的脂质组装体相互作用中的作用。研究结果将有助于提高对脂质界面的基本认识,并为相变作为对 NPs 暴露的响应策略的生物学功能提供新的见解。