Search results for "Branes"

showing 10 items of 525 documents

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
researchProduct

Polysialic acid can mediate membrane interactions by interacting with phospholipids

2009

Polysialic acid (polySia) is expressed on the surface of neural cells, neuroinvasive bacterial cells and several tumor cells. PolySia chains attached to NCAM can influence both trans interactions between membranes of two cells and cis interactions. Here, we report on the involvement of phospholipids in regulation of membrane interactions by polySia. The pH at the surface of liposomes, specific molecular area of phosphatidylcholine molecules, phase transition of DPPC bilayers, cyclic voltammograms of BLMs, and electron micrographs of phosphatidylcholine vesicles were studied after addition of polysialic acid free in solution. The results indicate that polySia chains can associate with phosph…

LiposomeChemistryPolysialic acidVesicleOrganic ChemistryPhospholipidMembranes ArtificialCell BiologyHydrogen-Ion ConcentrationBiochemistrychemistry.chemical_compoundSpectrometry FluorescenceMembraneMicroscopy Electron TransmissionBiochemistryPhosphatidylcholineSialic AcidsBiophysicsNeural cell adhesion moleculeAdsorptionLipid bilayerMolecular BiologyPhospholipidsChemistry and Physics of Lipids
researchProduct

Multipore membranes with nanofluidic diodes allowing multifunctional rectification and logical responses

2016

[EN] We have arranged two multipore membranes with conical nanopores in a three-compartment electrochemical cell. The membranes act as tunable nanofluidic diodes whose functionality is entirely based on the pH-reversed ion current rectification and does not require specific surface functionalizations. This electrochemical arrangement can display different electrical behaviors (quasi-linear ohmic response and inward/outward rectifications) as a function of the electrolyte concentration in the external solutions and the applied voltage at the pore tips. The multifunctional response permits to implement different logical responses including NOR and INHIBIT functions.

Logic functionsTechnologyMaterials sciencePhysics and Astronomy (miscellaneous)NanotechnologyNanofluidics02 engineering and technology010402 general chemistry01 natural sciencesElectrochemical cellEngineeringRectificationNanofluidic diodesMultipore membranesMultifunctional electrical responseOhmic contactApplied PhysicsDiodepH-reversed rectificationIon current021001 nanoscience & nanotechnology0104 chemical sciencesNanoporeMembraneFISICA APLICADAPhysical Sciences0210 nano-technologyApplied Physics Letters
researchProduct

Differences in the signaling pathways of α(1A)- and α(1B)-adrenoceptors are related to different endosomal targeting.

2013

AIMS: To compare the constitutive and agonist-dependent endosomal trafficking of α(1A)- and α(1B)-adrenoceptors (ARs) and to establish if the internalization pattern determines the signaling pathways of each subtype. METHODS: Using CypHer5 technology and VSV-G epitope tagged α(1A)- and α(1B)-ARs stably and transiently expressed in HEK 293 cells, we analyzed by confocal microscopy the constitutive and agonist-induced internalization of each subtype, and the temporal relationship between agonist induced internalization and the increase in intracellular calcium (determined by FLUO-3 flouorescence), or the phosphorylation of ERK1/2 and p38 MAP kinases (determined by Western blot). RESULTS AND C…

MAPK signaling cascadesEndosomemedia_common.quotation_subjecteducationIntracellular Spacelcsh:MedicineEndosomesSignal transductionERK signaling cascadeBiologyEndocytosisp38 Mitogen-Activated Protein KinasesSignaling PathwaysCell LineMolecular cell biologyReceptors Adrenergic alpha-1Calcium-Mediated Signal TransductionHumansMembrane Receptor SignalingCalcium SignalingInternalizationlcsh:ScienceBiologyCalcium signalingmedia_commonMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3MultidisciplinaryHEK 293 cellslcsh:RNeurotransmitter Receptor SignalingSignaling cascadesNeurotransmittersLipid signalingEndocytosisCell biologyTransport proteinProtein TransportHEK293 CellsCalcium signaling cascadeMembranes and Sortinglcsh:QAdrenergic alpha-1 Receptor AgonistsMolecular NeuroscienceSignal transductionResearch ArticleAdrenergic Signal TransductionNeurosciencePLoS ONE
researchProduct

Trefoil factor TFF1-induced protection of conjunctival cells from apoptosis at premitochondrial and postmitochondrial levels.

2008

PURPOSE. Goblet cells of the conjunctival epithelium synthesize and secrete TFF1 (Trefoil factor 1), a small protease-resistant peptide that, together with mucins, is responsible for the rheologic properties of the tear film. This study aimed to determine whether TFF1, whose synthesis increases in inflammatory conditions such as pterygium, could protect conjunctival cells from apoptosis. METHODS. Chang conjunctival cells, either wild-type or expressing TFF1 through stable transfection, were exposed to benzalkonium chloride (BAK) and ultraviolet (UV) irradiation to trigger apoptosis. The authors used cell fractionation to detect lipid raft‐associated proteins, coimmunoprecipitation to explor…

MESH : Cell LineMESH : Chromosomes Human Pair 21Chromosomes Human Pair 21CellApoptosisMESH: Flow CytometryMESH: Caspase 8Membrane Potentials0302 clinical medicineMESH: Mitochondrial MembranesMESH: Chromosomes Human Pair 21MESH : Membrane Potentials0303 health sciencesCaspase 8MESH : Caspase 8MESH : Benzalkonium CompoundsMESH : Tumor Suppressor ProteinsChromosome MappingFas receptorFlow CytometryXIAPMitochondriaMESH : Epithelial Cellsmedicine.anatomical_structureMESH: Epithelial Cells030220 oncology & carcinogenesisMitochondrial MembranesTrefoil Factor-1MESH : MitochondriaMESH : TransfectionBenzalkonium CompoundsConjunctivaMESH: Benzalkonium CompoundsProgrammed cell deathMESH: Enzyme ActivationMESH : ConjunctivaUltraviolet RaysMESH : Flow CytometryMESH: MitochondriaMESH: ConjunctivaCaspase 3BiologyInhibitor of apoptosisCaspase 8TransfectionCell Line03 medical and health sciencesMESH : Mitochondrial Membranesmedicine[SDV.BBM] Life Sciences [q-bio]/Biochemistry Molecular BiologyHumansMESH: Membrane PotentialsMESH: Tumor Suppressor Proteins[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular Biology[ SDV.BBM ] Life Sciences [q-bio]/Biochemistry Molecular Biology030304 developmental biologyMESH: HumansTumor Suppressor ProteinsMESH: ApoptosisMESH: TransfectionMESH : HumansEpithelial CellsMolecular biologyMESH: Cell LineEnzyme ActivationApoptosisMESH : Ultraviolet RaysMESH: Ultraviolet RaysMESH : Enzyme ActivationMESH: Chromosome MappingMESH : ApoptosisMESH : Chromosome Mapping
researchProduct

DNA nanofilm thickness measurement on microarray in air and in liquid using an atomic force microscope.

2005

International audience; The measurement of the thickness of DNA films on microarray as a function of the medium (liquid, air) is gaining importance for understanding the signal response of biosensors. Thiol group has been used to attach DNA strands to gold micropads deposited on silicon surface. Atomic force microscopy (AFM) was employed in its height mode to measure the change in the pad thickness and in its force mode to measure the indentation depth of the nanofilm. A good coherence between the height and force modes is observed for the film thickness in air. The adhesion force was found to be an alternative way to measure the surface coverage of the biolayer at nanoscopic scale. However…

MESH : Membranes ArtificialMESH: Materials TestingMESH : DNAMESH : Nucleic Acid ConformationAnalytical chemistryTissue Adhesions02 engineering and technologyMicroscopy Atomic Force01 natural sciencesCoated Materials BiocompatibleMESH: Coated Materials BiocompatibleIndentationMESH : Particle SizeMicroscopyMaterials TestingMESH : Coated Materials BiocompatibleElectrochemistryMESH : SolutionsMESH : Surface PropertiesComposite materialOligonucleotide Array Sequence AnalysisMESH: Microscopy Atomic ForceChemistryAirMESH: DNAGeneral Medicine021001 nanoscience & nanotechnologySolutionsMESH : Oligonucleotide Array Sequence AnalysisMembraneMESH: Nucleic Acid ConformationMESH : AirMESH: Membranes Artificial0210 nano-technologyBiotechnologySiliconSurface PropertiesBiomedical EngineeringBiophysicschemistry.chemical_elementMESH: Solutions010402 general chemistryMESH : Materials TestingAdsorptionMESH : Adsorption[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyMESH: Particle SizeParticle SizeNanoscopic scale[ SDV.BBM ] Life Sciences [q-bio]/Biochemistry Molecular BiologyMESH: Surface PropertiesMembranes ArtificialDNAMESH : Microscopy Atomic Force0104 chemical sciencesMESH : Tissue AdhesionsMESH: AirMESH: Oligonucleotide Array Sequence AnalysisNucleic Acid ConformationParticle sizeAdsorptionMESH: Tissue AdhesionsMESH: AdsorptionBiosensor
researchProduct

Early mitochondrial dysfunction, superoxide anion production, and DNA degradation are associated with non-apoptotic death of human airway epithelial …

2002

It has been shown that bacterial exoproducts may induce airway epithelium injury. During the epithelial repair process, the respiratory epithelial cells no more establish tight junctional intercellular complexes and may be particularly susceptible to bacterial virulence factors. In this study, we analyzed the effect of Pseudomonas aeruginosa exotoxin A (ETA) at different periods of time and concentrations on 16 HBE 14o(-) human bronchial epithelial cells in culture conditions inducing a phenotype of repairing cells. ETA treatment for 24 and 48 h led to the killing of 40.0 +/- 5.7% and 79.0 +/- 1.4% of the cells, respectively, as determined by the dimethylthiazole 2,5 diphenyl tetrazolium br…

MESH: Cell DeathMESH: ADP Ribose TransferasesMESH : DNAClinical BiochemistryCellApoptosisMESH : Dose-Response Relationship DrugMitochondrion[SDV.MHEP.PSR]Life Sciences [q-bio]/Human health and pathology/Pulmonology and respiratory tractMembrane PotentialsMESH: Dose-Response Relationship Drugchemistry.chemical_compoundSuperoxidesMESH: Intracellular MembraneMESH : DNA FragmentationRespiratory systemEnzyme InhibitorsCells CulturedADP Ribose TransferasesMESH : Cell SurvivalCell DeathSuperoxideMESH: DNAMESH: BronchiCaspase InhibitorsMESH : BronchiMitochondriaMESH : Epithelial Cellsmedicine.anatomical_structureMESH: Cell SurvivalMESH: Enzyme InhibitorsMESH: Epithelial CellsMESH : ADP Ribose TransferasesIntracellularMESH: Cells CulturedPulmonary and Respiratory MedicineProgrammed cell deathCell SurvivalVirulence FactorsBacterial ToxinsExotoxinsBronchiDNA FragmentationRespiratory MucosaBiologyMicrobiologyNecrosisNasal PolypsMESH : Cells CulturedmedicineHumansMESH: DNA FragmentationMESH : Intracellular MembraneMolecular BiologyMESH : Enzyme InhibitorsMESH: HumansMESH: CaspasesDose-Response Relationship DrugMESH: ApoptosisMESH : HumansEpithelial CellsCell BiologyDNAIntracellular MembranesMESH: ExotoxinschemistryMESH: Bacterial ToxinsApoptosisMESH : ExotoxinsMESH : Cell DeathMESH : Bacterial ToxinsRespiratory epithelium[SDV.MHEP.PSR] Life Sciences [q-bio]/Human health and pathology/Pulmonology and respiratory tractMESH : CaspasesMESH : Apoptosis[ SDV.MHEP.PSR ] Life Sciences [q-bio]/Human health and pathology/Pulmonology and respiratory tract
researchProduct

Ultrathin and nanostructured ZnO-based films for fluorescence biosensing applications

2011

The fluorescence-based sensing capability of ultrathin ZnO-SiO(2) nanoplatforms, deposited by an integrated approach of colloidal lithography and metal organic chemical vapor deposition, has been investigated upon adsorption of fluorescein-labeled albumin, used as model analyte biomolecule. The protein immobilization process after spontaneous adsorption/desorption significantly enhances the green emission of the different ZnO-based films, as evidenced by scanning confocal microscopy, corresponding to a comparable protein coverage detected by X-ray photoelectron spectroscopy. Moreover, experiments of fluorescence recovery after photobleaching evidence that the protein lateral diffusion at th…

MOCVD–colloidal lithography; Protein adsorption; Fluorescence recovery after photobleachingMaterials scienceSilicon dioxideMOCVD-colloidal lithographyZnO thin film; MOCVD-colloidal lithography; Biosensing; Protein adsorption; Fluorescence recovery after photobleachingProtein adsorptionNanotechnologyBiointerfaceBiosensing TechniquesChemical vapor depositionFluorescenceFluorescence recovery after photobleachingBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryAdsorptionX-ray photoelectron spectroscopyAlbuminschemistry.chemical_classificationBiosensingBiomoleculeMOCVD–colloidal lithographyMembranes ArtificialZnO thin filmSilicon DioxideNanostructuresSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryFluoresceinZinc OxideBiosensorProtein adsorptionJournal of Colloid and Interface Science
researchProduct

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
researchProduct

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
researchProduct