Plasma membranes sit at the divide – conceptually and literally – between the interior and exterior milieu of cells, coordinating communication between nearby cells and structuring surrounding tissue. While great effort over the last half century has advanced our understanding of the molecular organization of the plasma membrane, much of this work has focused on free plasma membranes that are not in contact with other cells. Recent studies have, however, highlighted unique and unexpected features of membrane interfaces between two cells, where the physical and chemical constraints of the interface conspire to create a system that is distinct from either plasma membrane alone. Inspired by this emerging view of cell-cell contacts, we propose classifying interfaces between cells as a distinct cellular compartment.
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http://dx.doi.org/10.1038/s41580-018-0057-3 | DOI Listing |
J Phys Chem Lett
January 2025
Soft Matter Biophysics, Institute for Condensed Matter Physics, TU Darmstadt, Hochschulstraße 8, 64289 Darmstadt, Germany.
Glycolipids are known to stabilize biomembrane multilayers through preferential sugar-sugar interactions that act as weak transient membrane cross-links. Here, we use small-angle and quasi-elastic neutron scattering on oligolamellar phospholipid vesicles containing defined glycolipid fractions in order to elucidate the influence of glycolipids on membrane mechanics and dynamics. Small-angle neutron scattering (SANS) reveals that the oligolamellar vesicles (OLVs) obtained by extrusion are polydisperse with regard to the number of lamellae, , which renders the interpretation of the quasi-elastic neutron spin echo (NSE) data nontrivial.
View Article and Find Full Text PDFLangmuir
January 2025
Department of Physics and Astronomy, University of Tennessee, Knoxville, Tennessee 37996, United States.
We demonstrate, using non-equilibrium molecular dynamics simulations, that lipid membrane capacitance varies with surface charge accumulation linked to membrane shape and curvature changes. Specifically, we show that lipid membranes exhibit a hysteretic response when exposed to oscillatory electric fields. The electromechanical coupling in these membranes leads to hysteretic buckling, in which the membrane can spontaneously buckle in one of two distinct directions along the electric field, even for the same ionic charge accumulation at the water-membrane interface.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Department of Stomatology, Zhongnan Hospital of Wuhan University, No. 169 Donghu Road, Wuhan 430071, China.
How to accurately diagnose and treat bacterial infections in vivo remains a huge challenge. Therefore, we have developed a targeted delivery nanosystem by coextruding the pretreated macrophage membrane of with carbon dots (M@CD). The M@CD nanosystem demonstrates potent antibacterial effects both in vivo and in vitro through the generation of reactive oxygen species (ROS).
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Division of Micro and Nanosystems (MST), School of Electrical Engineering and Computer Science (EECS), KTH Royal Institute of Technology, Stockholm SE-10044, Sweden.
Controlled breakdown has emerged as an effective method for fabricating solid-state nanopores in thin suspended dielectric membranes for various biomolecular sensing applications. On an unpatterned membrane, the site of nanopore formation by controlled breakdown is random. Nanopore formation on a specific site on the membrane has previously been realized using local thinning of the membrane by lithographic processes or laser-assisted photothermal etching under immersion in an aqueous salt solution.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Key Laboratory for Advanced Ceramics and Machining Technology of Ministry of Education, Institute of New-Energy, School of Materials Science and Engineering, Tianjin University, Tianjin 300072, China.
The development of water splitting technology in alkaline medium requires the exploration of electrocatalysts superior to Pt/C to boost the alkaline hydrogen evolution reaction (HER). Ruthenium oxides with strong water dissociation ability are promising candidates; however, the lack of hydrogen combination sites immensely limits their performance. Herein, we reported a unique RuO catalyst with metallic Ru on its surface through a simple cation exchange method.
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