Cardellini Jacopo, Caselli Lucrezia, Lavagna Enrico, Salassi Sebastian, Amenitsch Heinz, Calamai Martino, Montis Costanza, Rossi Giulia, Berti Debora
Department of Chemistry "Ugo Schiff" and CSGI, University of Florence, Via della Lastruccia 3, 50019 Sesto Fiorentino, Florence, Italy.
Department of Physics, University of Genoa, Genoa 16146, Italy.
J Phys Chem C Nanomater Interfaces. 2022 Mar 10;126(9):4483-4494. doi: 10.1021/acs.jpcc.1c08914. Epub 2022 Mar 1.
In recent years, many efforts have been devoted to investigating the interaction of nanoparticles (NPs) with lipid biomimetic interfaces, both from a fundamental perspective aimed at understanding relevant phenomena occurring at the nanobio interface and from an application standpoint for the design of novel lipid-nanoparticle hybrid materials. In this area, recent reports have revealed that citrate-capped gold nanoparticles (AuNPs) spontaneously associate with synthetic phospholipid liposomes and, in some cases, self-assemble on the lipid bilayer. However, the mechanistic and kinetic aspects of this phenomenon are not yet completely understood. In this study, we address the kinetics of interaction of citrate-capped AuNP with lipid vesicles of different rigidities (gel-phase rigid membranes on one side and liquid-crystalline-phase soft membranes on the other). The formation of AuNP-lipid vesicle hybrids was monitored over different time and length scales, combining experiments and simulation. The very first AuNP-membrane contact was addressed through molecular dynamics simulations, while the structure, morphology, and physicochemical features of the final colloidal objects were studied through UV-visible spectroscopy, small-angle X-ray scattering, dynamic light scattering, and cryogenic electron microscopy. Our results highlight that the physical state of the membrane triggers a series of events at the colloidal length scale, which regulate the final morphology of the AuNP-lipid vesicle adducts. For lipid vesicles with soft membranes, the hybrids appear as single vesicles decorated by AuNPs, while more rigid membranes lead to flocculation with AuNPs acting as bridges between vesicles. Overall, these results contribute to a mechanistic understanding of the adhesion or self-assembly of AuNPs onto biomimetic membranes, which is relevant for phenomena occurring at the nano-bio interfaces and provide design principles to control the morphology of lipid vesicle-inorganic NP hybrid systems.
近年来,人们致力于研究纳米颗粒(NPs)与脂质仿生界面的相互作用,这既出于旨在理解纳米生物界面发生的相关现象的基础研究视角,也出于设计新型脂质 - 纳米颗粒杂化材料的应用考量。在这一领域,近期报道显示柠檬酸盐包覆的金纳米颗粒(AuNPs)会自发地与合成磷脂脂质体缔合,在某些情况下还会在脂质双层上自组装。然而,这一现象的机理和动力学方面尚未完全明晰。在本研究中,我们探讨了柠檬酸盐包覆的AuNP与不同刚性的脂质囊泡(一侧为凝胶相刚性膜,另一侧为液晶相柔性膜)相互作用的动力学。结合实验与模拟,在不同的时间和长度尺度上监测AuNP - 脂质囊泡杂化物的形成。通过分子动力学模拟研究最初的AuNP - 膜接触,而通过紫外 - 可见光谱、小角X射线散射、动态光散射和低温电子显微镜研究最终胶体颗粒的结构、形态和物理化学特征。我们的结果表明,膜的物理状态在胶体长度尺度上引发了一系列事件,这些事件调节了AuNP - 脂质囊泡加合物的最终形态。对于具有柔性膜的脂质囊泡,杂化物表现为被AuNPs装饰的单个囊泡,而更刚性的膜则导致絮凝,AuNPs在囊泡之间起到桥梁作用。总体而言,这些结果有助于从机理上理解AuNPs在仿生膜上的粘附或自组装,这与纳米生物界面发生的现象相关,并为控制脂质囊泡 - 无机NP杂化系统的形态提供了设计原则。