Electrostatic interactions control the adsorption of extracellular vesicles onto supported lipid bilayers

被引:4
|
作者
Ridolfi, Andrea [1 ,2 ,3 ]
Cardellini, Jacopo [3 ,4 ]
Gashi, Fatlinda [5 ]
van Herwijnen, Martijn J. C. [6 ]
Trulsson, Martin [7 ]
Campos-Teran, Jose [8 ,9 ]
Wauben, Marca H. M. [6 ]
Berti, Debora [3 ,4 ]
Nylander, Tommy [5 ,9 ,10 ]
Stenhammar, Joakim [5 ]
机构
[1] Vrije Univ Amsterdam, Dept Phys & Astron, Amsterdam, Netherlands
[2] Vrije Univ Amsterdam, LaserLaB Amsterdam, Amsterdam, Netherlands
[3] Univ Florence, Dept Chem Ugo Schiff, Florence, Italy
[4] Univ Florence, CSGI, Consorzio Sistemi Grande Interfase, Sesto Fiorentino, Italy
[5] Lund Univ, Div Phys Chem, Lund, Sweden
[6] Univ Utrecht, Fac Vet Med, Dept Biomol Hlth Sci, Utrecht, Netherlands
[7] Lund Univ, Div Computat Chem, Lund, Sweden
[8] Univ Autonoma Metropolitana Cuajimalpa, Dept Proc & Tecnol, Mexico City, Mexico
[9] Inst Adv Neutron & X ray Sci, LINXS, Lund, Sweden
[10] Lund Univ, NanoLund, Lund, Sweden
关键词
RUPTURE; DNA; PHOSPHATIDYLCHOLINE; COMMUNICATION; SURFACES; ADHESION; FORCES;
D O I
10.1016/j.jcis.2023.07.018
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
Communication between cells located in different parts of an organism is often mediated by membrane-enveloped nanoparticles, such as extracellular vesicles (EVs). EV binding and cell uptake mechanisms depend on the heterogeneous composition of the EV membrane. From a colloidal perspective, the EV membrane interacts with other biological interfaces via both specific and non-specific interactions, where the latter include long-ranged electrostatic and van der Waals forces, and short -ranged repulsive "steric-hydration" forces. While electrostatic forces are generally exploited in most EV immobilization protocols, the roles played by various colloidal forces in controlling EV adsorption on surfaces have not yet been thoroughly addressed. In the present work, we study the adsorption of EVs onto supported lipid bilayers (SLBs) carrying different surface charge densities using a combination of quartz crystal microbalance with dissipation monitoring (QCM-D) and confocal laser scanning microscopy (CLSM). We demonstrate that EV adsorption onto lipid membranes can be controlled by varying the strength of electrostatic forces and we theoretically describe the observed phenomena within the framework of nonlinear Poisson-Boltzmann theory. Our modelling results confirm the experimental observations and highlight the crucial role played by attractive electrostatics in EV adsorption onto lipid membranes. They furthermore show that simplified theories developed for model lipid systems can be successfully applied to the study of their biological analogues and provide new fundamental insights into EV-membrane interactions with potential use in developing novel EV separation and immobilization strategies.
引用
收藏
页码:883 / 891
页数:9
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