ArticleACS applied materials & interfaces2020
Lipid Bicelle Micropatterning Using Chemical Lift-Off Lithography.
Article in ACS applied materials & interfaces, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed.
- Micropatterning of functional lipid bilayer assays for quantitative bioanalysis.Biomicrofluidics · 2023Article
- Domain Localization by Graphene Oxide in Supported Lipid Bilayers.International journal of molecular sciences · 2023Article
- Gap-directed chemical lift-off lithographic nanoarchitectonics for arbitrary sub-micrometer patterning.Beilstein journal of nanotechnology · 2023Article
- Lipid-Bicelle-Coated Microfluidics for Intracellular Delivery with Reduced Fouling.ACS applied materials & interfaces · 2020Article
- Versatile formation of supported lipid bilayers from bicellar mixtures of phospholipids and capric acid.Scientific reports · 2020Article
- Detecting DNA and RNA and Differentiating Single-Nucleotide Variations via Field-Effect Transistors.Nano letters · 2020Article
Corrections and comments
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Authors and funding
9 authors.
Funding
Abstract
Supported lipid membranes are versatile biomimetic coatings for the chemical functionalization of inorganic surfaces. Developing simple and effective fabrication strategies to form supported lipid membranes with micropatterned geometries is a long-standing challenge. Herein, we demonstrate how the combination of chemical lift-off lithography (CLL) and easily prepared lipid bicelle nanostructures can yield micropatterned, supported lipid membranes on gold surfaces with high pattern resolution, conformal character, and biofunctionality. Using CLL, we functionalized gold surfaces with patterned arrays of hydrophilic and hydrophobic self-assembled monolayers (SAMs). Time-lapse fluorescence microscopy imaging revealed that lipid bicelles adsorbed preferentially onto the hydrophilic SAM regions, while there was negligible lipid adsorption onto the hydrophobic SAM regions. Functional receptors could be embedded within the lipid bicelles, which facilitated selective detection of receptor-ligand binding interactions in a model streptavidin-biotin system. Quartz crystal microbalance-dissipation measurements further identified that lipid bicelles adsorb irreversibly and remain intact on top of the hydrophilic SAM regions. Taken together, our findings indicate that lipid bicelles are useful lipid nanostructures for reproducibly assembling micropatterned, supported lipid membranes with precise pattern fidelity.
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