Search results for "BILAYER"

showing 10 items of 391 documents

Altered pore-forming properties of proteolytically nicked staphylococcal alpha-toxin

1993

Staphylococcal alpha-toxin is a single-chain polypeptide with a molecular weight of 34,000 that hexamerizes in lipid bilayers to form pores of 1-1.5 nm effective diameter in membranes. We demonstrate that limited proteolysis of purified alpha-toxin with proteinase K generates a hemolytically active product that yields one major protein band of 17-18 kDa in SDS-polyacrylamide gel electrophoresis. The 17-18-kDa protein band harbors two major fragments of similar size representing the N- and C-terminal halves, which remain associated with each other in non-denaturing buffers but dissociate in 6 M urea. Dissociation in urea leads to loss of hemolytic activity. In contrast, unnicked alpha-toxin …

Staphylococcus aureusLysisProteolysisBacterial ToxinsHemolysin ProteinsHemolysisBiochemistryMonocytesCell membraneHemolysin ProteinsmedicineHumansLymphocytesLipid bilayerMolecular BiologyGel electrophoresismedicine.diagnostic_testbiologyCell MembraneErythrocyte MembraneSerine EndopeptidasesCell BiologyProteinase KPeptide FragmentsKineticsMembranemedicine.anatomical_structureBiochemistryChromatography Gelbiology.proteinElectrophoresis Polyacrylamide GelEndopeptidase KJournal of Biological Chemistry
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Lipid and phase specificity of α-toxin from S. aureus

2013

AbstractThe pore forming toxin Hla (α-toxin) from Staphylococcus aureus is an important pathogenic factor of the bacterium S. aureus and also a model system for the process of membrane-induced protein oligomerisation and pore formation. It has been shown that binding to lipid membranes at neutral or basic pH requires the presence of a phosphocholine-headgroup. Thus, sphingomyelin and phosphatidylcholine may serve as interaction partners in cellular membranes. Based on earlier studies it has been suggested that rafts of sphingomyelin are particularly efficient in toxin binding. In this study we compared the oligomerisation of Hla on liposomes of various lipid compositions in order to identif…

Staphylococcus aureusPore formationLiquid ordered phaseBacterial ToxinsLipid BilayersBiophysicsBiologyBiochemistryPhase Transitionchemistry.chemical_compoundHemolysin ProteinsMembrane LipidsMembrane MicrodomainsPhosphatidylcholineBinding siteLipid raftUnilamellar LiposomesPore-forming toxinLiposomeArtificial membranesBinding SitesCell MembraneOligomerisationCell BiologyS. aureusSphingomyelinsMembraneBiochemistrychemistryMicroscopy FluorescenceMutationPhosphatidylcholineslipids (amino acids peptides and proteins)Protein MultimerizationToxinSphingomyelinBiochimica et Biophysica Acta (BBA) - Biomembranes
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Staphylococcal alpha-toxin: formation of the heptameric pore is partially cooperative and proceeds through multiple intermediate stages.

1997

Staphylococcal alpha-toxin is a 293 residue polypeptide that assembles into pore-forming heptamers, residues 118-140, thereby inserting to form an amphipathic beta-barrel in the lipid bilayer. Fluorometric analyses were here conducted using cysteine-substitution mutants site-specifically-labeled at positions 35 or 130 with the environmentally-sensitive fluorophore acrylodan. In conjunction with functional assays, three conformational states of the heptamer were defined, which may represent transitional configurations of the toxin molecule along its way to membrane insertion and pore formation. The first was the freshly assembled, SDS-sensitive heptamer alpha7*a, where a minor alteration in …

Staphylococcus aureusProtein ConformationMutantBacterial ToxinsLipid BilayersExotoxinsSequence (biology)ProtomerBiochemistryResidue (chemistry)Hemolysin ProteinsProtein structureBacterial Proteins2-NaphthylamineAmphiphileAnimalsAmino Acid SequenceLipid bilayerFluorescent DyesChemistryErythrocyte MembraneMembraneSpectrometry FluorescenceBiophysicsMutagenesis Site-DirectedRabbitsBiochemistry
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Dynamics of Pattern Formation in Biomimetic Systems

2008

This paper is an attempt to conceptualize pattern formation in self-organizing systems and, in particular, to understand how structures, oscillations or waves arise in a steady and homogenous environment, a phenomenon called symmetry breaking. The route followed to develop these ideas was to couple chemical oscillations produced by Belousov-Zhabotinsky reaction with confined reaction environments, the latter being an essential requirement for any process of Life. Special focus was placed on systems showing organic or lipidic compartments, which represent more reliable biomimetic matrices.

Statistics and Probability{CHEMICAL} {OSCILLATORS}Belousov-Zhabotinsky reactionLipid BilayersPattern formationNanotechnology{CHEMICAL} {OSCILLATORS}; Lipid systems; Reverse microemulsionsModels BiologicalTuring structuresGeneral Biochemistry Genetics and Molecular BiologyDiffusionBiomimeticsChemical oscillatorsAnimalsSymmetry breakingPhysicsGeneral Immunology and MicrobiologyChemistry PhysicalSystems BiologyApplied MathematicsLipid systemsBiomimetic systemsGeneral MedicineBelousov-Zhabotinsky reaction; Chemical oscillators; Turing structures; Biomimetic systems; Lipid systems; Reverse microemulsionsReverse microemulsionsBelousov–Zhabotinsky reactionModeling and SimulationEmulsionsGeneral Agricultural and Biological SciencesBiological system
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Putative identification of an amphipathic alpha-helical sequence in hemolysin of Escherichia coli (HlyA) involved in transmembrane pore formation.

2008

Abstract Escherichia coli hemolysin is a pore-forming protein belonging to the RTX toxin family. Cysteine scanning mutagenesis was performed to characterize the putative pore-forming domain of the molecule. A single cysteine residue was introduced at 48 positions within the sequence spanning residues 170–400 and labeled with the polarity-sensitive dye badan. Spectrofluorimetric analyses indicated that several amino acids in this domain are inserted into the lipid bilayer during pore formation. An amphipathic α-helix spanning residues 272–298 was identified that may line the aqueous pore. The importance of this sequence was highlighted by the introduction of two prolines at positions 284 and…

StereochemistryClinical BiochemistryAmino Acid MotifsPorinsmedicine.disease_causeBiochemistryProtein Structure SecondaryHemolysin ProteinsCell Line TumormedicineAnimalsHumansLipid bilayerMolecular BiologyEscherichia colichemistry.chemical_classificationEscherichia coli ProteinsRTX toxinMutagenesisErythrocyte MembraneHemolysinTransmembrane proteinAmino acidchemistryMutant ProteinsRabbitsCysteineBiological chemistry
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Electrostatic Contribution to the Surface Pressure of Charged Monolayers Containing Polyphosphoinositides

2008

Structural and functional studies of lateral heterogeneity in biological membranes have underlined the importance of membrane organization in biological function. Most inquiries have focused on steric determinants of membrane organization, such as headgroup size and acyl-chain saturation. This manuscript reports a combination of theory and experiment that shows significant electrostatic contributions to surface pressures in monolayers of phospholipids where the charge spacing is smaller than the Bjerrum length. For molecules with steric cross sections typical of phospholipids in the cell membrane (approximately 50 A(2)), only polyphosphoinositides achieve this threshold. The most abundant s…

Steric effectsModels MolecularMembrane FluiditySurface PropertiesLipid BilayersStatic ElectricityBiophysics010402 general chemistryBjerrum length01 natural sciences03 medical and health sciencesPhosphatidylinositol PhosphatesMonolayerMembrane fluidityPressureComputer SimulationLipid bilayer030304 developmental biology0303 health sciencesChromatographyMembranesHydrogen bondChemistryBiological membrane0104 chemical sciencesModels ChemicalChemical physicsIonic strength
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Investigation of Temperature-Induced Phase Transitions in DOPC and DPPC Phospholipid Bilayers Using Temperature-Controlled Scanning Force Microscopy

2004

Under physiological conditions, multicomponent biological membranes undergo structural changes which help define how the membrane functions. An understanding of biomembrane structure-function relations can be based on knowledge of the physical and chemical properties of pure phospholipid bilayers. Here, we have investigated phase transitions in dipalmitoylphosphatidylcholine (DPPC) and dioleoylphosphatidylcholine (DOPC) bilayers. We demonstrated the existence of several phase transitions in DPPC and DOPC mica-supported bilayers by both atomic force microscopy imaging and force measurements. Supported DPPC bilayers show a broad L(beta)-L(alpha) transition. In addition to the main transition …

Steric effectsPhase transition12-DipalmitoylphosphatidylcholineBiophysicsPhospholipid02 engineering and technologyMicroscopy Atomic Force010402 general chemistry01 natural sciencesPhase TransitionQuantitative Biology::Subcellular Processeschemistry.chemical_compoundTransition TemperaturePhospholipidsPhysics::Biological PhysicsMembranesBilayerTransition temperaturedigestive oral and skin physiologyBiological membrane021001 nanoscience & nanotechnology0104 chemical sciencesCondensed Matter::Soft Condensed MatterCrystallographyMembranechemistryChemical physicsDipalmitoylphosphatidylcholineAluminum Silicateslipids (amino acids peptides and proteins)0210 nano-technologyBiophysical Journal
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Protein-membrane interaction probed by single plasmonic nanoparticles.

2008

We present a nanosized and addressable sensor platform based on membrane coated plasmonic particles and show unequivocally the covering with lipid bilayers as well as the subsequent detection of streptavidin binding to biotinylated lipids. The binding is detected on membrane covered gold nanorods by monitoring the spectral shift by fast single particle spectroscopy (fastSPS) on many particles in parallel. Our approach allows for local analysis of protein interaction with biological membranes as a function of the lateral composition of phase separated membranes.

StreptavidinMaterials scienceNanoparticleMolecular Probe TechniquesBioengineeringNanotechnologyResonance (particle physics)Spectral lineQuantitative Biology::Subcellular Processeschemistry.chemical_compoundProtein Interaction MappingGeneral Materials ScienceSurface plasmon resonanceSpectroscopyLipid bilayerPlasmonPlasmonic nanoparticlesbusiness.industryChemistryMechanical EngineeringCell MembraneMembrane ProteinsBiological membraneGeneral ChemistrySurface Plasmon ResonanceCondensed Matter PhysicsDark field microscopyMembraneTransmission electron microscopyBiotinylationParticleOptoelectronicsNanoparticlesbusinessNano letters
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Molecular mechanisms determining the strength of receptor-mediated intermembrane adhesion

1995

The strength of receptor-mediated cell adhesion is directly controlled by the mechanism of cohesive failure between the cell surface and underlying substrate. Unbinding can occur either at the locus of the specific bond or within the bilayer, which results in tearing the hydrophobic anchors from the membrane interior. In this work, the surface force apparatus has been used to investigate the relationship between the receptor-ligand bond affinities and the dominant mechanism of receptor-coupled membrane detachment. The receptors and ligands used in this study were membrane-bound streptavidin and biotin analogs, respectively, with solution affinities ranging over 10 orders of magnitude. With …

StreptavidinStereochemistryLipid BilayersMolecular ConformationBiophysicsReceptors Cell Surface02 engineering and technologyModels BiologicalCell membrane03 medical and health scienceschemistry.chemical_compoundBacterial ProteinsmedicineCell AdhesionAnimalsBond energyLipid bilayer030304 developmental biologyFluorescent Dyes0303 health sciencesThioctic AcidBilayerPhosphatidylethanolaminesCell MembraneSurface forces apparatus021001 nanoscience & nanotechnologyAffinitiesModels StructuralKineticsmedicine.anatomical_structureMembranechemistryBiophysicsStreptavidin0210 nano-technologyAzo CompoundsResearch ArticleBiophysical Journal
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Bilayer Formation of Streptavidin Bridged by Bis(biotinyl) Peptide at the Air/Water Interface

1994

Streptavidinchemistry.chemical_classificationchemistry.chemical_compoundColloid and Surface ChemistrychemistryAir water interfaceBilayerPolymer chemistryOrganic chemistryPeptideGeneral ChemistryBiochemistryCatalysisJournal of the American Chemical Society
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