Membrane Phase Drives the Assembly of Gold Nanoparticles on Biomimetic Lipid Bilayers

被引:22
|
作者
Cardellini, Jacopo [1 ,2 ]
Caselli, Lucrezia [1 ,2 ]
Lavagna, Enrico [3 ]
Salassi, Sebastian [3 ]
Amenitsch, Heinz [4 ]
Calamai, Martino [5 ]
Montis, Costanza [1 ,2 ]
Rossi, Giulia [3 ]
Berti, Debora [1 ,2 ]
机构
[1] Univ Florence, Dept Chem Ugo Schiff, I-50019 Sesto Fiorentino, Italy
[2] Univ Florence, CSGI, I-50019 Sesto Fiorentino, Italy
[3] Univ Genoa, Dept Phys, I-16146 Genoa, Italy
[4] Graz Univ Technol, Inst Inorgan Chem, A-8010 Graz, Austria
[5] European Lab Nonlinear Spect LENS, I-50019 Sesto Fiorentino, Italy
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2022年 / 126卷 / 09期
基金
欧盟地平线“2020”; 欧洲研究理事会;
关键词
LIPOSOMES; CITRATE; SIZE; MAGNETOLIPOSOMES; SEPARATION; MODEL; DLS;
D O I
10.1021/acs.jpcc.1c08914
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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.
引用
收藏
页码:4483 / 4494
页数:12
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