Search results for "POPC"

showing 10 items of 18 documents

Lateral organization of G M1 in phase-separated monolayers visualized by scanning force microscopy

2002

Phase separation of glycolipids in lipid mono- and bilayers is of great interest for the understanding of membrane function. The distribution of the ganglioside GM1 in sphingomyelin (SM)/1-palmitoyl-2-oleoyl- sn-glycero-3-phosphocholine (POPC), SM/1,2-dipalmitoyl- sn-glycero-3-phosphocholine (DOPC) and SM/cholesterol/POPC Langmuir-Blodgett (LB) monolayers transferred at 36 mN/m has been studied by scanning force microscopy. Besides lateral organization of the glycolipid in LB monolayers as deduced from topography, material properties have been investigated by phase imaging, pulsed force mode and force modulation microscopy. It was shown that GM1 preferentially clusters in an ordered lipid m…

Aqueous solutionChemistryLipid BilayersBiophysicsAnalytical chemistryBrainMembranes ArtificialG(M1) GangliosideGeneral MedicineMicroscopy Atomic ForceLipidsMicelleSphingomyelinschemistry.chemical_compoundCrystallographyCholesterolGlycolipidPhase (matter)MicroscopyMonolayerPhosphatidylcholinesSphingomyelinPOPCEuropean Biophysics Journal
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Roles of a conserved proline in the internal fusion peptide of Ebola glycoprotein

2004

AbstractThe structural determinants underlying the functionality of viral internal fusion peptides (IFPs) are not well understood. We have compared EBOwt (GAAIGLAWIPYFGPAAE), representing the IFP of the Ebola fusion protein GP, and EBOmut (GAAIGLAWIPYFGRAAE) derived from a non-functional mutant with conserved Pro537 substituted by Arg. P537R substitution did not abrogate peptide-membrane association, but interfered with the ability to induce bilayer destabilization. Structural determinations suggest that Pro537 is required to preserve a membrane-perturbing local conformation in apolar environments.

Circular dichroismEbola glycoproteinProtein insertion into membranesProlinePeptide conformationMutantMolecular Sequence DataBiophysicsBiochemistrySendai viruschemistry.chemical_compoundStructural BiologyGeneticsProlineAmino Acid SequenceMolecular BiologyPeptide sequencePOPCchemistry.chemical_classificationChemistryProteïnes de membranaCell BiologyEbolavirusFusion proteinPeptide FragmentsPeptide ConformationViral fusion peptideBiochemistryAvian Sarcoma VirusesLiposomesHIV-1PèptidsGlycoproteinPeptide–lipid interactionViral Fusion ProteinsFEBS Letters
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Structure Of Complexes Of Helix-5 From Bax With Lipid Membranes

2009

Bax is a proapoptotic protein implicated in the release of cell-death activating factors from the mitochondrial intermembrane space. Although the structure of the membrane-bound forms of Bax is unknown, it has been proposed to form proteolipidic pores. Studies with synthetic lipid vesicles have shown that fragments encompassing helix-5 of Bax retain a membrane permeabilization ability that is similar to that of the full-length protein. Here we report on the structure of peptide-membrane complexes formed by a Bax helix-5 peptide and lipid bilayers. The relative orientation of the peptide and the lipids are determined using site-specific infrared spectroscopy, assisted by isotopic labeling of…

Crystallographychemistry.chemical_compoundMembraneChemistryMitochondrial intermembrane spaceBilayerMembrane fluidityBiophysicsBiological membraneLipid bilayer phase behaviorLipid bilayerPOPCBiophysical Journal
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Time-resolved fluorescence and fourier transform infrared spectroscopic investigations of lateral packing defects and superlattice domains in composi…

2003

Time-resolved fluorescence and Fourier transform infrared spectroscopies were used to investigate the lateral organization of lipids in compositionally uniform and fully equilibrated 1-palmitoyl-2-oleoyl-phosphatidylcholine/cholesterol (POPC/CHOL) liposomes prepared by a recently devised low-temperature trapping method. Independent fluorescence decay lifetime and rotational dynamics parameters of diphenylhexatriene (DPH) chain-labeled phosphatidylcholine (DPH-PC) in these liposomes were recovered from the time-resolved fluorescence measurements as a function of cholesterol molar fraction (X(CHOL)) at 23 degrees C. The results indicate significantly greater lifetime heterogeneity, shorter av…

DiphenylhexatrieneModels MolecularMacromolecular SubstancesMembrane FluidityLipid BilayersBiophysicsAnalytical chemistry010402 general chemistryMole fraction01 natural sciences03 medical and health scienceschemistry.chemical_compoundPhosphatidylcholineSpectroscopy Fourier Transform InfraredMembrane fluiditypolycyclic compoundsComputer SimulationLipid bilayerPOPCRotational correlation time030304 developmental biology0303 health sciencesLiposomeMembranestechnology industry and agricultureSignal Processing Computer-Assisted0104 chemical sciencesCrystallographyCholesterolSpectrometry FluorescencechemistryLiposomesPhosphatidylcholinesAnisotropylipids (amino acids peptides and proteins)AlgorithmsBiophysical journal
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Bis(imidazolium) salts derived from amino acids as receptors and transport agents for chloride anions

2015

The binding properties of bis(imidazolium) hosts 1a–c derived from amino acids towards different anions have been studied by 1H NMR titration experiments in 95 : 05 CD3CN : H2O at 303 K, ESI-MS and theoretical calculations. Among this family, the salt 1c showed a strong and high selectivity for chloride anions. Transmembrane chloride transport activity has also been studied for the three bis(imidazolium) based transporters in POPC liposome models, and compound 1a was identified as an active chloride/nitrate exchanger.

General Chemical EngineeringChemistry OrganicSalt (chemistry)Medicinal chemistryChlorideCompostos orgànics Síntesichemistry.chemical_compoundmedicineLife ScienceOrganic chemistryPOPCVLAGchemistry.chemical_classificationLiposomeamino acidsOrganic Chemistrychloride anionsQuímica orgánicaGeneral ChemistryOrganische ChemieTransmembrane proteinAmino acidchemistryProton NMRbis(imidazolium)TitrationAminoàcidsmedicine.drug
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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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Nanoparticle structure development in the gastro‐intestinal model fluid FaSSIF mod6.5 from several phospholipids at various water content relevant fo…

2014

The characteristics of intestinal model fluids were investigated at conditions, which simulate the passage from the middle to the end of the duodenum. The formation and decay of liposomes and micelles in model bile fluids were studied, because of their role as an intermediate host for the resolution and uptake of hydrophobic drugs (BCS classes II, IV). The conditions, which may influence the formation of these nanoparticulate intermediates were studied, i.e., the lipid composition of the bile, the preparation method, the time of the passage through the modelled duodenum segment and the concentration, which results from the variable dilution of the bile by mixing with the transfer medium rep…

LiposomeChromatographyfood.ingredientChemistryKineticsGeneral ChemistryLecithinMicelleIndustrial and Manufacturing EngineeringDilutionchemistry.chemical_compoundmedicine.anatomical_structurefoodIn vivoDuodenummedicinelipids (amino acids peptides and proteins)POPCFood ScienceBiotechnologyEuropean Journal of Lipid Science and Technology
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Microstructuring of phospholipid bilayers on gold surfaces by micromolding in capillaries

2005

Microstructuring of lipid bilayers on gold surfaces was achieved by micromolding in capillaries employing chemically modified polydimethylsiloxane (PDMS). Microfluidic networks of PDMS were prepared by micromolding and functionalized with thiol end-groups using 3-mercaptopropyltrimethoxysilane. The PDMS stamps were firmly attached to the gold substrate via quasi-covalent linkage providing a tight seal, a prerequisite for establishing individual addressable capillaries. Bilayers composed of POPC/POPG were subsequently prepared on microstructured self assembly monolayers of 11-amino-1-undecanethiol via strong electrostatic interactions. This way it is possible to generate individually address…

Materials sciencePolydimethylsiloxaneLipid BilayersMicrofluidicsMicrofluidicsSiliconestechnology industry and agriculturePDMS stampNanotechnologyMicroscopy Atomic ForceSoft lithographySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundColloid and Surface ChemistrychemistryMonolayerDimethylpolysiloxanesGoldSelf-assemblyLipid bilayerPOPCPhospholipidsJournal of Colloid and Interface Science
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Phase coexistence in a triolein-phosphatidylcholine system. Implications for lysosomal membrane properties.

2010

The effects of tri- and monoglycerides on phospholipid (POPC) membranes were studied using spectroscopical methods. Triolein was found to form two types of POPC-rich membranes, both with POPC or as a three-component system with monopalmitin. These two membrane types were determined as co-existing phases based on their spontaneous and stable separation and named heavy and light phase according to their sedimentation behaviour. Marked differences were seen in the physical properties of these phases, even though only minor compositional variation was detected. The light, less polar phase was found to be less ordered and more fluid and seemed to allow significantly lower amount of water penetra…

Membrane FluidityLipid BilayersPhospholipidCalorimetryBiochemistryPhase TransitionGlycerideschemistry.chemical_compoundPhosphatidylcholineMembrane fluidityTransition TemperatureTrioleinMolecular BiologyPOPCChromatographyCalorimetry Differential ScanningOrganic ChemistryElectron Spin Resonance SpectroscopyWaterCell BiologyPenetration (firestop)MembranechemistryBiophysicsPhosphatidylcholineslipids (amino acids peptides and proteins)LysosomesTrioleinChemistry and physics of lipids
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Regulation of Calcium Channel Activity by Lipid Domain Formation in Planar Lipid Bilayers

2003

The sarcoplasmic reticulum channel (ryanodine receptor) from cardiac myocytes was reconstituted into planar lipid bilayers consisting of 1-palmitoyl-2-oleoyl-phosphatidylethanolamine (POPE) and 1-palmitoyl-2-oleoyl-phosphatidylcholine (POPC) in varying ratios. The channel activity parameters, i.e., open probability and average open time and its resolved short and long components, were determined as a function of POPE mole fraction (X(PE)) at 22.4 degrees C. Interestingly, all of these parameters exhibited a narrow and pronounced peak at X(PE) approximately 0.80. Differential scanning calorimetric measurements on POPE/POPC liposomes with increasing X(PE) indicated that the lipid bilayer ente…

Membrane FluidityProtein ConformationLipid BilayersBiophysicsAnalytical chemistryMolecular Conformation010402 general chemistryElectric Capacitance01 natural sciencesMembrane Potentials03 medical and health scienceschemistry.chemical_compoundStructure-Activity RelationshipProtein structureMembrane MicrodomainsChannels Receptors and TransportersMembrane fluidityLipid bilayer phase behaviorLipid bilayerPOPC030304 developmental biologyMembrane potential0303 health sciencesLiposomeEndoplasmic reticulumPhosphatidylethanolaminesMembranes ArtificialRyanodine Receptor Calcium Release Channel0104 chemical scienceschemistry13. Climate actionBiophysicsPhosphatidylcholineslipids (amino acids peptides and proteins)Calcium ChannelsIon Channel Gating
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