Search results for "Lipid bilayers"

showing 10 items of 135 documents

Incorporation of the acetylcholine receptor dimer from Torpedo californica in a peptide supported lipid membrane investigated by surface plasmon and …

1998

Abstract The dimer species (Mr 580 000) of the nicotinic acetylcholine receptor, isolated from the electric organ of Torpedo californica, was incorporated into a thiopeptide supported lipid bilayer. The incorporation was achieved by fusion of liposomes with reconstituted receptor onto a gold-supported thiopeptide lipid monolayer. Surface plasmon resonance spectroscopy (SPS) was used to monitor in real time the fusion process as well as the specific binding of the antagonist α-bungarotoxin. A recently developed extension of SPS offering enhanced sensitivity and specificity, surface plasmon fluorescence spectroscopy (SPFS), was then used to monitor subsequent binding of the monoclonal WF6 and…

Electric OrganLiposomeChemistryLipid BilayersSurface plasmonBiomedical EngineeringBiophysicsMembranes ArtificialGeneral MedicineReceptors NicotinicSurface Plasmon ResonanceTorpedoFluorescence spectroscopylaw.inventionNicotinic acetylcholine receptorSpectrometry FluorescenceBiochemistrylawElectrochemistryAnimalsLipid bilayerTorpedoIon channelBiotechnologyAcetylcholine receptorBiosensors and Bioelectronics
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Flotillin-involved uptake of silica nanoparticles and responses of an alveolar-capillary barrier in vitro

2013

AbstractDrug and gene delivery via nanoparticles across biological barriers such as the alveolar-capillary barrier of the lung constitutes an interesting and increasingly relevant field in nanomedicine. Nevertheless, potential hazardous effects of nanoparticles (NPs) as well as their cellular and systemic fate should be thoroughly examined. Hence, this study was designed to evaluate the effects of amorphous silica NPs (Sicastar) and (poly)organosiloxane NPs (AmOrSil) on the viability and the inflammatory response as well as on the cellular uptake mechanisms and fate in cells of the alveolar barrier. For this purpose, the alveolar epithelial cell line (NCI H441) and microvascular endothelial…

EndosomeCell SurvivalLipid BilayersPharmaceutical ScienceGene deliverysilica nanoparticlesEndocytosisClathrinNP transportCell LineDrug Delivery SystemsAlveolar-capillary barrierAlveolar capillary barrierElectric ImpedanceHumansColoring AgentsInflammationFlotillin-1/-2-dependent uptake/traffickingbiologyChemistryRhodaminesVesicleMicrocirculationEndothelial CellsMembrane ProteinsGeneral Medicinerespiratory systemSilicon DioxideNP uptakeIn vitroCoculture TechniquesEndocytosisCapillariesEndothelial stem cellPulmonary AlveoliNP-transportNanomedicineCell cultureImmunologybiology.proteinBiophysicsNanoparticlesBiotechnologyEuropean Journal of Pharmaceutics and Biopharmaceutics
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Transmembrane beta-barrel of staphylococcal alpha-toxin forms in sensitive but not in resistant cells.

1997

Staphylococcal α-toxin is a 293-residue, single-chain polypeptide that spontaneously assembles into a heptameric pore in target cell membranes. To identify the pore-forming domain, substitution mutants have been produced in which single cysteine residues were introduced throughout the toxin molecule. By attaching the environmentally sensitive dye acrylodan to the sulfhydryl groups, the environment of individual amino acid side chains could be probed. In liposomes, a single 23-amino acid sequence (residues 118–140) was found to move from a polar to a nonpolar environment, indicating that this sequence forms the walls of the pore. However, periodicity in side chain environmental polarity coul…

ErythrocytesNeutrophilsStaphylococcusT-LymphocytesBacterial ToxinsLipid BilayersBiologyHemolysin ProteinsCell membraneHemolysin ProteinsAdenosine TriphosphatePhagocytosismedicineAnimalsHumansCysteineLipid bilayerchemistry.chemical_classificationLiposomeMultidisciplinaryCell MembraneBiological SciencesFlow CytometryTransmembrane proteinRecombinant ProteinsAmino acidmedicine.anatomical_structureBeta barrelchemistryBiochemistryAmino Acid SubstitutionMutagenesis Site-DirectedPotassiumRabbitsCysteine
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Relationship between the structure of amphiphilic copolymers and their ability to disturb lipid bilayers.

2005

Nonionic amphiphiles and particularly block copolymers of ethylene oxide and propylene oxide (Pluronics) cause pronounced chemosensitization of tumor cells that exhibit multiple resistance to antineoplastic drugs. This effect is due to inhibition of P-glycoprotein (P-gp) responsible for drug efflux. It was suggested that the inhibition of P-gp might be due to changes in its lipid surrounding. Indeed, high dependence of P-gp activity on the membrane microviscosity was demonstrated [Regev et al. (1999) Eur. J. Biochem. 259, 18-24], suggesting that the ability of Pluronics to affect the P-gp activity is mediated by their effect on the membrane structure. We have found recently that adsorption …

Ethylene OxideGlycerolFree RadicalsPolymersLipid BilayersPoloxamerBiochemistryPermeabilityPolyethylene GlycolsMicroviscositychemistry.chemical_compoundStructure-Activity RelationshipAmphiphilePolymer chemistryCopolymerAnimalsHexanesLipid bilayerLiposomeEthylene oxideWaterMembranes ArtificialPoloxamerMembranechemistryDoxorubicinLiposomesBiophysicsPhosphatidylcholinesEpoxy CompoundsCattleAdsorptionBiochemistry
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N- and O-methylation of sphingomyelin markedly affects its membrane properties and interactions with cholesterol

2011

We have prepared palmitoyl sphingomyelin (PSM) analogs in which either the 2-NH was methylated to NMe, the 3-OH was methylated to OMe, or both were methylated simultaneously. The aim of the study was to determine how such modifications in the membrane interfacial region of the molecules affected interlipid interactions in bilayer membranes. Measuring DPH anisotropy in vesicle membranes prepared from the SM analogs, we observed that methylation decreased gel-phase stability and increased fluid phase disorder, when compared to PSM. Methylation of the 2-NH had the largest effect on gel-phase instability (T(m), was lowered by similar to 7 degrees C). Atomistic molecular dynamics simulations sho…

Hydrogen bondingLipid BilayersBiophysicsSterol partitioningMethylationBiochemistryMembrane Lipidschemistry.chemical_compoundAmideMolecular dynamics simulationOrganic chemistryMoleculeAcyl chain orderMolecular StructureHydrogen bondChemistryVesicleBilayerTemperatureta1182MethylationCell BiologySphingomyelinsKineticsSterolsCholesterolMembraneLateral domainsBiophysicsAnisotropySphingomyelinBiochimica et Biophysica Acta (BBA) - Biomembranes
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Kinetics of the lipoperoxyl radical-scavenging activity of indicaxanthin in solution and unilamellar liposomes

2007

Abstract The reaction of the phytochemical indicaxanthin with lipoperoxyl radicals generated in methyl linoleate methanol solution by 2,20-azobis(2,4-dimethylvaleronitrile), and in aqueous soybean phosphatidylcholine unilamellar liposomes by 2,20-azobis(2- amidinopropane)hydrochloride, was studied. The molecule acts as a chain-terminating lipoperoxyl radical scavenger in solution, with a calculated inhibition constant of 3.63 £ 105M21 s21, and a stoichiometric factor approaching 2. Indicaxanthin incorporated in liposomes prevented lipid oxidation, inducing clear-cut lag periods and decrease of the propagation rate. Both effects were concentration-dependent, but not linearly related to the p…

Indicaxanthin membranes radical scavenger liposomesLipid PeroxidesAntioxidant12-DipalmitoylphosphatidylcholinePyridinesmedicine.medical_treatmentRadicalLipid Bilayersalpha-TocopherolAmidinesContext (language use)In Vitro TechniquesBiochemistryAntioxidantsLipid peroxidationchemistry.chemical_compoundLipid oxidationSuspensionsPhosphatidylcholineNitrilesmedicineOrganic chemistryLiposomeDose-Response Relationship DrugMolecular StructureMethanolDrug SynergismGeneral MedicineFree Radical ScavengersBetaxanthinsSolutionsKineticschemistryLinoleic AcidsLiposomesPhosphatidylcholinesSolventsLipid PeroxidationIndicaxanthinAzo CompoundsOxidation-ReductionNuclear chemistry
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Unsaturated Fatty Acids Drive Disintegrin and Metalloproteinase (ADAM)-dependent Cell Adhesion, Proliferation, and Migration by Modulating Membrane F…

2011

The disintegrin-metalloproteinases ADAM10 and ADAM17 mediate the release of several cell signaling molecules and cell adhesion molecules such as vascular endothelial cadherin or L-selectin affecting endothelial permeability and leukocyte transmigration. Dysregulation of ADAM activity may contribute to the pathogenesis of vascular diseases, but the mechanisms underlying the control of ADAM functions are still incompletely understood. Atherosclerosis is characterized by lipid plaque formation and local accumulation of unsaturated free fatty acids (FFA). Here, we show that unsaturated FFA increase ADAM-mediated substrate cleavage. We demonstrate that these alterations are not due to genuine ch…

KeratinocytesMembrane FluidityADAM10Lipid BilayersVascular permeabilityBiologyADAM17 ProteinBiochemistryCapillary PermeabilityADAM10 ProteinCell MovementMembrane fluidityCell AdhesionAnimalsHumansCell adhesionMolecular BiologyCell ProliferationCell adhesion moleculeCell growthFluorescence recovery after photobleachingEndothelial CellsMembrane ProteinsCell BiologyAtherosclerosisADAM ProteinsCell biologyLipoproteins LDLADAM ProteinsHEK293 CellsFatty Acids UnsaturatedCholesterol EstersRabbitsAmyloid Precursor Protein SecretasesGranulocytes
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Pulmonary surfactant protein C containing lipid films at the air-water interface as a model for the surface of lung alveoli.

1995

The pulmonary surfactant lines as a complex monolayer of lipids and proteins the alveolar epithelial surface. The monolayer dynamically adapts the surface tension of this interface to the varying surface areas during inhalation and exhalation. Its presence in the alveoli is thus a prerequisite for a proper lung function. The lipid moiety represents about 90% of the surfactant and contains mainly dipalmitoylphosphatidylcholine (DPPC) and phosphatidylglycerol (PG). The surfactant proteins involved in the surface tension adaption are called SP-A, SP-B and SP-C. The aim of the present investigation is to analyse the properties of monolayer films made from pure SP-C and from mixtures of DPPC, DP…

LangmuirChemical PhenomenaSurface PropertiesProteolipidsLipid BilayersMolecular Sequence DataBiophysicsPalmitic AcidsBiophysical PhenomenaSurface tensionchemistry.chemical_compoundPulmonary surfactantEllipsometryMonolayerHumansPulmonary surfactant-associated protein CAmino Acid SequenceMolecular BiologyPhospholipidsPhosphatidylglycerolChemistryChemistry PhysicalAirtechnology industry and agricultureWaterMembranes ArtificialPulmonary SurfactantsCell BiologyLipid MetabolismLipidsPulmonary AlveoliCrystallographyChemical engineeringDipalmitoylphosphatidylcholinelipids (amino acids peptides and proteins)Protein BindingMolecular membrane biology
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Interactions of liposomes and hydrophobically-modified poly-(N-isopropylacrylamides): an attempt to model the cytoskeleton

1993

The interactions of small unilamellar vesicles (SUV) and water-soluble copolymers were studied by fluorescence spectroscopy, differential scanning calorimetry (DSC) and quasi-elastic light scattering (QELS). The anchoring onto liposomal bilayer membranes of copolymers of N-isopropylacrylamide, N-(2-(1-naphthyl)ethyl)-N-n-octadecylacrylamide and or N-[4-(1-pyrenyl)butyl]-N-n-octadecylacrylamide (0.5 mol% of the octadecylacrylamide comonomer) was monitored by non-radiative energy transfer between excited naphthalene and pyrene. The anchoring process occurred on zwitterionic lecithin liposomes and on negatively charged phosphatidic acid liposomes, whether the bilayer was in the crystalline or …

Lipid BilayersAcrylic ResinsBiophysicsSynthetic membranePhosphatidic AcidsModels BiologicalBiochemistryLower critical solution temperatureStructure-Activity Relationshipchemistry.chemical_compoundDifferential scanning calorimetryCopolymerOrganic chemistryCytoskeletonchemistry.chemical_classificationLiposomeBilayerComonomerCell BiologyPolymerchemistryChemical engineeringLiposomesPhosphatidylcholinesThermodynamicsDimyristoylphosphatidylcholineBiochimica et Biophysica Acta (BBA) - Biomembranes
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Spectrophotometric evidence for the solubilization site of betalain pigments in membrane biomimetic systems.

2007

The solubilization site of two betalain pigments, namely, betanin and indicaxantin, into l-alpha-dipalmitoyl-phosphatidylcholine (DPPC) and dimyristoylphosphatidylcholine (DMPC) vesicles was investigated by a spectrophotometric study. Pigment absorbance was monitored by varying phospholipid concentration, at a constant temperature that was varied in a range including the main phase transition temperature (Tm) of the relevant phospholipid bilayer. Maximum betanin absorption increased with the increase of DPPC concentration within the entire temperature range, reaching a plateau. The binding constant (Kb) of the pigment, calculated according to a pseudo-two-phase model, varied with the temper…

Lipid BilayersBetalainsPigmentchemistry.chemical_compoundBetalainvesiclePhospholipidsBetaninChromatographyChemistryVesicletechnology industry and agricultureGeneral Chemistrybetalain pigmentMembraneSolubilitySolubilizationSpectrophotometrybio-mimetic membranesvisual_artLiposomesvisual_art.visual_art_mediumBetalain Pigmentslipids (amino acids peptides and proteins)General Agricultural and Biological SciencesIndicaxanthinJournal of agricultural and food chemistry
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