Search results for "Lipid bilayers"

showing 10 items of 135 documents

Quantification of the Raf-C1 Interaction With Solid-Supported Bilayers

2002

By use of the quartz crystal microbalance technique, the interaction of the Raf-Ras binding domain (RafRBD) and the cysteine-rich domain Raf-C1 with lipids was quantified by using solid-supported bilayers immobilized on gold electrodes deposited on 5 MHz quartz plates. Solid-supported lipid bilayers were composed of an initial octanethiol monolayer chemisorbed on gold and a physisorbed phospholipid monolayer varying in its lipid composition as the outermost layer. The integrity of bilayer preparation was monitored by impedance spectroscopy. For binding experiments, a protein construct comprising the RafRBD and Raf-C1 linked to the maltose binding protein and a His tag, termed MBP-Raf-C1, wa…

Lipid BilayersPhospholipidBiosensing TechniquesMicroscopy Atomic ForceBiochemistrychemistry.chemical_compoundMonolayerLipid bilayerMolecular BiologyBilayerOrganic ChemistryUnithiolQuartz crystal microbalanceProtein Structure TertiaryProto-Oncogene Proteins c-rafDissociation constantCrystallographychemistryThermodynamicsMolecular Medicinelipids (amino acids peptides and proteins)AdsorptionGoldDimyristoylphosphatidylcholineProtein adsorptionBinding domainChemBioChem
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In situ synthesis of lipopeptides as versatile receptors for the specific binding of nanoparticles and liposomes to solid-supported membranes.

2008

A detailed study of the in situ coupling of small peptides such as CGGH6 (H6) and CGWK8 (K8) to maleimide functionalized phospholipid bilayers is presented. Individually addressable microstructured membranes are employed to unequivocally probe the conjugation. The in situ coupling of peptides via a terminal cysteine moiety to maleimide functionalized phospholipids is shown to be a convenient and versatile way to selectively fabricate peptide-modified phospholipid bilayers serving as specific receptor platforms for functionalized vesicles and nanoparticles. Specific binding of functional vesicles to the peptide-modified bilayers is achieved by either histidine complexation with Ni-NTA-DOGS c…

Lipid BilayersStatic ElectricityPhospholipidBiomaterialsDiffusionMaleimideschemistry.chemical_compoundMoietyOrganic chemistryNanotechnologyGeneral Materials ScienceCysteineLipid bilayerMaleimidePOPCMicellesPhospholipidsLiposomeMicroscopy ConfocalChemistryVesicleLysineWaterGeneral ChemistryMembraneModels ChemicalLiposomesBiophysicsNanoparticlesPeptidesBiotechnologySmall (Weinheim an der Bergstrasse, Germany)
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Reaction of melatonin with lipoperoxyl radicals in phospholipid bilayers.

1997

Melatonin, at 5 to 500 microM was incorporated in unilamellar soybean phosphatidylcholine (PC) liposomes, the peroxidation of which was induced by 2,2'-azobis (2-amidinopropane-hydrochloride) (AAPH), and measured as production of conjugated diene lipid hydroperoxides. Concentration as low as 5 and 10 microM were poorly effective in reducing lipid peroxidation. Melatonin at 30 to 500 microM caused short inhibition periods, increasing with, but not linearly related to concentration, with a concurrent net decrease of the propagation rate. The time course of melatonin oxidation, measured as loss of fluorescence, was studied during the AAPH-stimulated peroxidation of soybean PC liposomes, or whe…

Lipid PeroxidesAntioxidantFree Radicalsmedicine.medical_treatmentLipid BilayersPhospholipidPhotochemistryBiochemistryMelatoninLipid peroxidationchemistry.chemical_compoundPhysiology (medical)PhosphatidylcholinemedicineVitamin ETocopherolMelatoninLiposomeVitamin EDrug SynergismFree Radical ScavengersKineticschemistryBiophysicsPhosphatidylcholinesLipid PeroxidationOxidation-Reductionhormones hormone substitutes and hormone antagonistsmedicine.drugFree radical biologymedicine
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Interaction of Quinine with Model Lipid Membranes of Different Compositions

2002

The binding of a drug such as Quinine with neutral and negatively charged small unilamellar lipid vesicles at pH 7 and 37 degrees C was investigated. Changes in the fluorescence properties of the drug after association with the liposomes were used to obtain binding isotherms over a range of phospholipid compositions at different ionic strengths. Under such conditions, the association was strongly enhanced by the negative net charge of the bilayer but diminished by the increasing presence of electrolytes in the aqueous media. Binding data were analyzed in terms of a surface partition equilibrium without and after correcting for electrostatic effects by means of the Gouy-Chapman theory. The i…

LiposomeBinding SitesChromatographyQuinineChemistryBilayerLipid BilayersStatic ElectricityPhospholipidPharmaceutical ScienceMembranes ArtificialPhosphatidylglycerolsBinding constantPartition coefficientHydrophobic effectchemistry.chemical_compoundIonic strengthPartition equilibriumBiophysicsJournal of Pharmaceutical Sciences
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The impact of humic and fulvic acids on the dynamic properties of liposome membranes: the ESR method

2013

This paper presents the results of research on the influence of two fractions of humic substances (HS): fulvic acids (FA) and humic acids (HA), as a function of concentration, on the liposome membranes formed from egg yolk lecithin (EYL). The concentration of HS in relation to EYL changed from 0% to 10% by weight. The influence of HS on various areas of membranes: interphase water-lipid, in the lipid layer just below the polar part of the membrane and in the middle of the lipid bilayer, was investigated by different spin labels (TEMPO, DOXYL 5, DOXYL 16). The study showed that HA slightly decreased the fluidity of the analyzed membranes on the surface layer, while FA significantly liquidate…

LiposomeChromatographyfood.ingredientESR methodFree RadicalsMembrane FluidityChemistryhumic substancesRadicalLipid BilayersElectron Spin Resonance SpectroscopyPharmaceutical ScienceLecithinKineticsfoodMembraneYolkLiposomesBenzopyransSpin LabelsInterphaseEYL liposomesSurface layerLipid bilayerNuclear Magnetic Resonance BiomolecularJournal of Liposome Research
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Electrically induced deformation of giant liposomes monitored by thickness shear mode resonators.

2006

Thickness shear mode resonators are capable of registering small changes in the thickness and viscoelastic properties of ultrathin films attached to their surface. It was found that it is possible to monitor the deformation of surface-bound giant liposomes by applying an electric field with small amplitudes. Changes in the apparent height of attached vesicles in the nanometer range were easily detected as a function of lipid composition. Increasing the bending modulus by adding cholesterol results in a significantly reduced deformation from 16.8 nm (5% cholesterol) down to 3.2 nm (20% cholesterol), rendering this new method a robust and sensitive tool to detect the bending elasticity of lip…

LiposomeMaterials scienceFlexural modulusbusiness.industrySurface PropertiesVesicleLipid BilayersSurfaces and InterfacesCondensed Matter PhysicsViscoelasticityElasticityResonatorOpticsCholesterolShear (geology)Electric fieldLiposomesElectrochemistryPhosphatidylcholinesGeneral Materials ScienceNanometreComposite materialbusinessSpectroscopyLangmuir : the ACS journal of surfaces and colloids
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Identification of a putative membrane-inserted segment in the alpha-toxin of Staphylococcus aureus.

1994

To gain a fuller understanding of the regions of the Staphylococcus aureus alpha-toxin important in pore formation, we have used Forster dipole-dipole energy transfer to demonstrate that a central glycine-rich region of alpha-toxin (the so-called "hinge" region) inserts deeply into the bilayer on association of toxin with liposomes. Mutant alpha-toxins with unique cysteine (C) residues at positions 69 and 130 [Palmer, M., et al. (1993) J. Biol. Chem. 268, 11959) were reacted with the C-specific fluorophore acrylodan, which acted as an energy donor. The chosen acceptor was N-(7-nitrobenz-2-oxa-13- diazol-4-yl)-1,2-bis(hexadecanoyl)-sn-glycero-3-phosphoethanolamin e (NBD-PE). Measurement of t…

LiposomeStaphylococcus aureusQuenching (fluorescence)FluorophoreStereochemistryBilayerPhosphatidylethanolaminesBacterial ToxinsLipid BilayersMembrane ProteinsFluorescence PolarizationBiochemistryAcceptorLipidschemistry.chemical_compoundHemolysin ProteinsMembranechemistryMutagenesis Site-DirectedStaphylococcus aureus delta toxinCysteineFluorescent DyesBiochemistry
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Membrane fluidity and the surface properties of the lipid bilayer: ESR experiment and computer simulation

2009

Penetration of the liposome membranes formed in the gel phase from DPPC (DPPC liposomes) and in the liquid-crystalline phase from egg yolk lecithin (EYL liposomes) by the TEMPO (2,2,6,6-tetramethylpiperidine-1-oxyl) and 16 DOXYL (2-ethyl-2-(15-methoxy-oxopentadecyl)-4,4-dimethyl-3-oxazolidinyloxy) spin probes has been investigated. The penetration process was followed by 120 hours at 24(0)C, using the electron spin resonance (ESR) method. The investigation of the kinetics of the TEMPO probe building into the membranes of both types of liposomes revealed differences appearing 30 minutes after the start of the experiment. The number of TEMPO particles built into the EYL liposome membranes beg…

Liposomefood.ingredient12-DipalmitoylphosphatidylcholineMembrane FluiditySurface PropertiesChemistryBilayerLipid BilayersElectron Spin Resonance SpectroscopyAnalytical chemistryPharmaceutical SciencePenetration (firestop)Lecithinlaw.inventionCyclic N-OxidesMembranefoodlawMembrane fluidityComputer SimulationSpin LabelsLipid bilayerElectron paramagnetic resonanceMonte Carlo MethodJournal of Liposome Research
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Scrutiny of the Failure of Lipid Membranes As A Function of Headgroups, Chain Length, and Lamellarity Measured by Scanning Force Microscopy

2004

AbstractA fast, quantitative, and unambiguous screening of material properties of biomembranes using scanning force microscopy in pulsed force mode on lipid membranes is presented. The spatially resolved study of breakthrough force, breakthrough distance, adhesion, stiffness, and topography of lipid membranes as determined simultaneously by digitalized pulsed force mode provides new insight into the structure-function relationship of model membranes, which are systematically analyzed by varying chain length, lipid headgroup, and lamellarity. For this purpose, a novel unbiased analysis method is presented. A strong correlation between adhesion and breakthrough events is found on lipid bilaye…

Macromolecular SubstancesMembrane FluidityLipid BilayersBiophysicsAnalytical chemistryMolecular ConformationMicroscopy Atomic ForceMicromanipulationMotionStructure-Activity RelationshipMicroscopyMaterials TestingmedicineMembrane fluidityLipid bilayerLiposomeMembranesChemistrytechnology industry and agricultureStiffnessMembranes ArtificialElasticityMembraneStructural stabilityLiposomesBiophysicslipids (amino acids peptides and proteins)Stress Mechanicalmedicine.symptomMaterial properties
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Partitioning of Pyrene-Labeled Phospho- and Sphingolipids between Ordered and Disordered Bilayer Domains

2004

AbstractHere we have studied how the length of the pyrene-labeled acyl chain (n) of a phosphatidylcholine, sphingomyelin, or galactosylceramide affects the partitioning of these lipids between 1), gel and fluid domains coexisting in bovine brain sphingomyelin (BB-SM) or BB-SM/spin-labeled phosphatidylcholine (PC) bilayers or 2), between liquid-disordered and liquid-ordered domains in BB-SM/spin-labeled PC/cholesterol bilayers. The partitioning behavior was deduced either from modeling of pyrene excimer/monomer ratio versus temperature plots, or from quenching of the pyrene monomer fluorescence by spin-labeled PC. New methods were developed to model excimer formation and pyrene lipid quenchi…

Macromolecular SubstancesMembrane FluidityLipid BilayersMolecular ConformationBiophysicsPhase Transition03 medical and health scienceschemistry.chemical_compoundMembrane MicrodomainsPhosphatidylcholineMembrane fluidityFluorometryLipid bilayerPhospholipids030304 developmental biologySphingolipids0303 health sciencesPyrenesMembranesQuenching (fluorescence)Staining and LabelingChemistry030302 biochemistry & molecular biologyTemperatureBiological membraneModels ChemicalBiochemistryDipalmitoylphosphatidylcholineLiposomesBiophysicsPyrenelipids (amino acids peptides and proteins)SphingomyelinBiophysical Journal
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