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A simple Giant unilamellar vesicle (sGUV) is a micron-sized spherical vesicle, which is composed of a lipid bilayer that encloses an aqueous solution inside and is suspended in another aqueous medium. As biomimetic models of biological cells, sGUVs are well-established systems for biophysical studies. However, sGUVs primarily mimic anucleate cells, limiting their application as models for non-nucleate cells. We propose compound Giant Unilamellar vesicles (cGUVs) as a more appropriate biomimetic model for nucleated cells. cGUVs are vesicle-in-vesicle structures, where the outer and inner vesicle bilayers can be assumed to represent the cell and the nuclear membrane of a cell, respectively. In this study, we describe a simple method for the synthesis of cGUVs. Briefly, sGUVs were generated using the lipid composition of DMPC and cholesterol within the range of 37-43 mol% in a sucrose medium via the electroformation method. These sGUVs were then subjected to osmotic shock by introducing a hypertonic glucose solution, triggering an immediate transition to a somatocytic shape. This process led to the formation of an intermediate state where the outer and inner vesicles remained connected through a neck, ultimately resulting in the development of vesicle-in-vesicle structure, referred to as cGUVs. Furthermore, it is known that GUVs prepared with higher cholesterol levels in the bilayer exhibit reduced ion permeability. This characteristic allows tuning of conductivity in the annular solution of a cGUV by adjusting the conductivities of the hydrating medium, the inner solution through hypertonic glucose, and the outer solution by adjusting of the dilution or the addition of conductive media, making the resultant cGUVs with controlled conductivities in the outer, annular, and inner regions, relevant for electric field studies. We propose this efficient and straightforward approach for synthesizing compound vesicles that can be used as a biomimetic model for eukaryotic, nucleated cells, advancing their application in biophysical research.
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http://dx.doi.org/10.3791/68274 | DOI Listing |
J Am Chem Soc
September 2025
Life-like Materials and Systems, University of Mainz, Duesbergweg 10-14, 55128 Mainz, Germany.
Transmembrane signaling is essential for cellular communication, yet reconstituting such mechanisms in synthetic systems remains challenging. Here, we report a simple and robust DNA-based mechanism for transmembrane signaling in synthetic cells using cholesterol-modified single-stranded DNA (Chol-ssDNA). We discovered that anchored Chol-ssDNA spontaneously flips across the membrane of giant unilamellar lipid vesicles (GUVs) in a nucleation-driven, defect-mediated process.
View Article and Find Full Text PDFAutophagy
September 2025
Department of Chemistry, Dartmouth College, Hanover, NH, USA.
Macroautophagy (hereafter, autophagy) is essential for the degradation of mitochondria from yeast to humans. Mitochondrial autophagy in yeast is initiated when the selective autophagy scaffolding protein Atg11 is recruited to mitochondria through its interaction with the selective autophagy receptor Atg32. This also results in the recruitment of small 30-nm vesicles that fuse to generate the initial phagophore membrane.
View Article and Find Full Text PDFBiophys J
September 2025
Department of Engineering Sciences and Applied Mathematics, Northwestern University, IL 60208, USA. Electronic address:
The physical properties of lipid membranes are essential to cellular function, with membrane fluidity playing a key role in the mobility of embedded biomolecules. Fluidity is governed by the membrane's phase state, which is known to depend on composition and temperature. However, in living cells, the transmembrane electric potential may also influence membrane fluidity.
View Article and Find Full Text PDFBiomolecules
August 2025
Departamento de Bioquímica, Instituto de Química, Universidade de São Paulo, São Paulo 05508-220, Brazil.
Antimicrobial peptides (AMPs) are a primary defense against pathogens. Here, we examined the interaction of two BP100 analogs, RR-BP100 (where Arg substitutes Lys 2 and 5) and RR-BP100-A-NH-C (where an Ala and a C hydrocarbon chain are added to the RR-BP100 C-terminus), with membrane models. Large unilamellar vesicles (LUVs) and giant unilamellar vesicles (GUVs) were prepared with the major lipids in Gram-positive (GP) and Gram-negative (GN) bacteria, as well as red blood cells (RBCs).
View Article and Find Full Text PDFChem Sci
August 2025
Institute of Physiological Chemistry and Pathobiochemistry, University of Münster Münster Germany
Cell motility is a fundamental process involved in many complex cellular events and the development of synthetic cells that mimic cell motility enables us to understand the composite mechanisms underlying it. Here, we use giant unilamellar vesicles (GUVs) and supported lipid bilayers (SLBs) as simplified models to investigate how the surface density of ligands and their lateral mobility influences adhesion-dependent cell motility. In particular, we use the photoswitchable interactions between the proteins iLID (improved light-inducible dimer) and nano (wild-type SspB) to induce light-responsive adhesions of the GUVs on the SLBs and systematically tune adhesion properties by varying receptor and ligand densities, and assess their effects on the reversibility and dynamics of adhesion.
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