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Assembly of Cell Mimicking Supported and Suspended Lipid Bilayer Models for the Study of Molecular Interactions
Published on: August 3, 2021
Interaction of imidazolium-based ionic liquids with supported phospholipid bilayers as model biomembranes
Massimiliano Galluzzi1,2, Lorenzo Marfori2, Stefania Asperti2
1Materials Interfaces Center, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, Guangdong, China. galluzzi@siat.ac.cn.
Insights
Ionic liquids (ILs) can alter cell membranes, affecting their structure and mechanical properties. This study used atomic force microscopy to reveal how ILs interact with lipid bilayers, offering insights for designing safer ILs.
Area of Science:
- Biophysics
- Materials Science
- Toxicology
Background:
- Ionic liquids (ILs) are increasingly used, raising concerns about their biological and environmental impact.
- The cell membrane is a primary target for ILs, but nanoscale toxicity mechanisms remain unclear.
Purpose of the Study:
- To investigate the effects of room-temperature ionic liquids (ILs) on the mechanical, morphological, and electrostatic properties of phospholipid bilayers using atomic force microscopy (AFM).
- To understand the concentration- and time-dependent changes in lipid membranes exposed to various imidazolium-based ILs.
Main Methods:
- Utilized atomic force microscopy (AFM) to probe solid-supported dipalmitoylphosphatidylcholine (DOPC) phospholipid bilayers.
- Analyzed changes in membrane morphology, nanomechanics (breakthrough force, Young's modulus, area stretching modulus), and surface electrostatics.
Main Results:
- Ionic liquids restructured lipid bilayers, forming new IL/lipid complexes with increased area and roughness.
- IL exposure progressively reduced membrane rigidity and structural ordering, evidenced by decreased mechanical properties.
- AFM detected a reduction in negative surface charge density, indicating cation stratification on the membrane surface.
Conclusions:
- Ionic liquids significantly alter the physical and chemical properties of model biomembranes at the nanoscale.
- Findings provide a foundation for designing ionic liquids with controlled interactions with biological membranes, potentially mitigating toxicity.
Abstract:
The cytotoxicity of ionic liquids (ILs) has been receiving attention in the context of the biological and environmental impact of their vast field of applications. It has been ascertained that the cell membrane is the main target of ILs when they interact with microorganisms, cells and bacteria; nevertheless, studies at the micro- and nano-scale aiming at better understanding of the fundamental mechanisms of toxicity of ILs are lacking. In this work, we used atomic force microscopy (AFM) to investigate the impact of room-temperature ILs on the mechanical, morphological and electrostatic properties of solid-supported DOPC phospholipid bilayers, taken as models of biomembranes. In particular, we have characterized the concentration-dependent and time-dependent evolution of the morphological, structural and mechanical properties of DOPC lipid membranes in the presence of imidazolium-based ILs with different alkyl chain lengths and hydrophilic/hydrophobic characteristics. The majority of ILs investigated were found to possess the ability of restructuring the lipid bilayer, through the formation of new IL/lipid complexes, showing distinctive morphological features (increase of area and roughness). The nanomechanical analysis of the lipid membrane exposed to ILs revealed a progressive, concentration-dependent perturbation of the structural ordering and rigidity of the membrane, evidenced by a decrease in the breakthrough force, Young's modulus and area stretching modulus. AFM detected a modification of the electrostatic double-layer at the membrane surface, in terms of a reduction of the original negative surface charge density, suggesting a progressive stratification of cations on the exposed leaflet of the lipid membrane. Our findings may be helpful in designing novel ILs with tailored interaction with biological membranes.
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