The present work explores the properties for binary (LA/DPPC), (cholesterol/DPPC) and also ternary (LA/cholesterol/DPPC) mixed Langmuir monolayers, at the air-water interface, treated as the simplest models of a half of the biological membranes. In ternary monolayers both cholesterol and DPPC were mixed at constant molar ratios that correspond to the proportions occuring in different natural membranes, among which fibroblast membrane (where the amount of phospholipid predominates) and also erythrocyte membrane (where the amount of sterol predominates) were taken into consideration. Our researches were conducted by using the Langmuir film balance, by means of which we registered the surface pressure (pi) as a function of the area of water surface available to each molecule (A). It was found that LA and DPPC also cholesterol and DPPC are miscible in binary as well as LA, cholesterol and DPPC in ternary mixed monolayers, however in ternary mixed monolayers, at higher content of fatty acid (for molar fraction X(LA)=0.6, 0.8) these components were miscible only at the surface pressure below approximately 27 mN/m. Furthermore the results of our measurements show that LA reveals very strong influence on the membrane composition. Depending on various amounts of this fatty acid within the models of biological membranes it seems to affect different stability of natural bilayer.
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http://dx.doi.org/10.1016/j.colsurfb.2009.01.005 | DOI Listing |
J Phys Chem B
January 2025
Institute of Chemical Kinetics and Combustion, Russian Academy of Sciences, Novosibirsk 630090, Russia.
Plasma membranes are known to segregate into liquid disordered and ordered nanoscale phases, the latter being called lipid rafts. The structure, lipid composition, and function of lipid rafts have been the subject of numerous studies using a variety of experimental and computational methods. Double electron-electron resonance (DEER, also known as PELDOR) is a member of the pulsed dipole EPR spectroscopy (PDS) family of techniques, allowing the study of nanoscale distances between spin-labeled molecules.
View Article and Find Full Text PDFJ Phys Chem B
January 2025
Department of Chemistry, University of Tennessee, Knoxville, Tennessee 37916, United States.
Eukaryotic plasma membranes exhibit nanoscale lateral lipid heterogeneity, a feature that is thought to be central to their function. Studying these heterogeneities is challenging since few biophysical methods are capable of detecting domains at submicron length scales. We recently showed that cryogenic electron microscopy (cryo-EM) can directly image nanoscale liquid-liquid phase separation in extruded liposomes due to its ability to resolve the intrinsic thickness and electron density differences of ordered and disordered phases.
View Article and Find Full Text PDFJ Agric Food Chem
December 2024
Department of Food Science and Technology, Zhejiang University of Technology, Hangzhou, Zhejiang 310014, People's Republic of China.
Cholesterol (Cho) is commonly used to stabilize nanoliposomes; however, there is controversy on the relationship between Cho and health. In this study, we developed a novel multifunctional nanoliposome utilizing structurally similar sitogluside (SG) and dioscin (Dio) instead of Cho to anchor the phospholipid bilayer and synergistically modulate the membrane properties of the nanoliposome (DPPC or DOPC). The storage and gastrointestinal tract stability experiment demonstrated that the changes of physical and chemical properties, including the significantly reduced size and Dio retention rate of nanoliposomes synergistically modulated by SG and Dio compared to those of SG alone, regulated nanoliposomes.
View Article and Find Full Text PDFBiochim Biophys Acta Biomembr
December 2024
Applied Biophysics and Food Research Center (Centro de Investigaciones en Biofísica Aplicada y Alimentos, CIBAAL, National University of Santiago del Estero and CONICET), RN 9 - Km 1125, 4206 Santiago del Estero, Argentina. Electronic address:
Langmuir
December 2024
Sao Carlos Institute of Physics, University of Sao Paulo, CP 369, 13560-970 São Carlos, SP, Brazil.
The design of chemotherapeutic drug carriers requires precise information on their interaction with the plasma membrane since the carriers should be internalized by cells without disrupting or compromising the overall integrity of the membrane. In this study, we employ Langmuir monolayers mimicking the outer leaflet of plasma membranes of healthy and cancerous cells to determine the molecular-level interactions with a water-soluble calixarene derivative, -sulfonic acid calix[4]arene (SCX4), which is promising as drug carrier. The cancer membrane models comprised either 40% 1,2-dipalmitoyl--glycero-3-phosphocholine (DPPC) or 1,2-dioleoyl--glycero-3-phosphocholine (DOPC), 30% cholesterol (Chol), 20% 1,2-dipalmitoyl--glycero-3-phosphoethanolamine (DPPE), and 10% 1,2-dipalmitoyl--glycero-3-phospho-l-serine (DPPS).
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