Search results for "bonding"

showing 10 items of 996 documents

An efficient dissipative particle dynamics-based algorithm for simulating electrolyte solutions

2015

We propose an efficient simulation algorithm based on the dissipative particle dynamics (DPD) method for studying electrohydrodynamic phenomena in electrolyte fluids. The fluid flow is mimicked with DPD particles while the evolution of the concentration of the ionic species is described using Brownian pseudo particles. The method is designed especially for systems with high salt concentrations, as explicit treatment of the salt ions becomes computationally expensive. For illustration, we apply the method to electro-osmotic flow over patterned, superhydrophobic surfaces. The results are in good agreement with recent theoretical predictions.

Models MolecularOsmosisMaterials scienceSurface PropertiesGeneral Physics and AstronomyIonic bondingFOS: Physical sciencesElectrolyteCondensed Matter - Soft Condensed MatterIonPhysics::Fluid DynamicsElectrolytesFluid dynamicsPhysical and Theoretical ChemistryBrownian motionDissipative particle dynamicsFluid Dynamics (physics.flu-dyn)MechanicsPhysics - Fluid DynamicsComputational Physics (physics.comp-ph)SolutionsCondensed Matter::Soft Condensed MatterFlow (mathematics)HydrodynamicsSoft Condensed Matter (cond-mat.soft)SaltsElectrohydrodynamicsPhysics - Computational PhysicsHydrophobic and Hydrophilic InteractionsAlgorithms
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Origins of fluorescence in evolved bacteriophytochromes

2014

Use of fluorescent proteins to study in vivo processes in mammals requires near-infrared (NIR) biomarkers that exploit the ability of light in this range to penetrate tissue. Bacteriophytochromes (BphPs) are photoreceptors that couple absorbance of NIR light to photoisomerization, protein conformational changes, and signal transduction. BphPs have been engineered to form NIR fluorophores, including IFP1.4, Wi-Phy, and the iRFP series, initially by replacement of Asp-207 by His. This position was suggestive because its main chain carbonyl is within hydrogen-bonding distance to pyrrole ring nitrogens of the biliverdin chromophore, thus potentially functioning as a crucial transient proton sin…

Models MolecularPhotoisomerizationNitrogenSurface PropertiesQuantum yieldCrystallography X-RayLigandsProtein EngineeringPhotochemistryBiochemistrychemistry.chemical_compoundparasitic diseasesSide chainAnimalsCloning MolecularneoplasmsMolecular BiologySpectroscopy Near-InfraredBiliverdinBacteriaPhytochromeChemistryBiliverdinetechnology industry and agricultureta1182WaterHydrogen BondingCell BiologyChromophoreequipment and suppliesFluorescenceProtein Structure Tertiarysurgical procedures operativeSpectrometry FluorescenceStructural biologySpectrophotometryProtein Structure and FoldingPhytochromeHydrophobic and Hydrophilic InteractionsBiomarkersProtein BindingJournal of Biological Chemistry
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2NH and 3OH are crucial structural requirements in sphingomyelin for sticholysin II binding and pore formation in bilayer membranes.

2013

AbstractSticholysin II (StnII) is a pore-forming toxin from the sea anemone Stichodactyla heliantus which belongs to the large actinoporin family. The toxin binds to sphingomyelin (SM) containing membranes, and shows high binding specificity for this lipid. In this study, we have examined the role of the hydrogen bonding groups of the SM long-chain base (i.e., the 2NH and the 3OH) for StnII recognition. We prepared methylated SM-analogs which had reduced hydrogen bonding capability from 2NH and 3OH. Both surface plasmon resonance experiments, and isothermal titration calorimetry measurements indicated that StnII failed to bind to bilayers containing methylated SM-analogs, whereas clear bind…

Models MolecularPore Forming Cytotoxic ProteinsMembrane permeabilizationLipid BilayersBiophysicsCalorimetryta3111Biochemistrychemistry.chemical_compoundCnidarian VenomsAnimalsComputer SimulationLipid bilayerta116Binding selectivityUnilamellar LiposomesPhosphocholineBinding SitesMolecular StructureChemistryHydrogen bondVesicleta1182Isothermal titration calorimetryHydrogen BondingCell BiologySurface Plasmon ResonanceProtein Structure TertiarySphingomyelinsKineticsMembraneSea AnemonesBiochemistryMolecular dockingIsothermal titration calorimetryBiophysicsPhosphatidylcholinesSphingomyelinProtein BindingBiochimica et biophysica acta
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Exploring the redox reactivity of magnesium porphine. Insight into the origins of electropolymerisation.

2010

International audience; Magnesium(II) porphine, MgP (1), was synthesised according to the Lindsey procedure allowing to isolate and crystallise 1-formyldipyrromethane (2) as a synthetic intermediate. Unprecedented Xray diffraction studies revealed multiple intermolecular associations in the crystal between neighbouring units of 2, namely hydrogen bond and CH … π. The electrochemical behaviour of 1 was examined by means of cyclic voltammetry. In oxydation, two well-defined and distinct steps are assigned to macrocycle concerned electron transfers yielding initially the π-cation radical and π dication, respectively. The highly reactive dication condenses neutral magnesium porphine to form a d…

Models MolecularPorphyrinsInorganic chemistrychemistry.chemical_element010402 general chemistryElectrochemistryCrystallography X-Ray01 natural sciencesRedoxOligomerInorganic Chemistrychemistry.chemical_compound[CHIM.ANAL]Chemical Sciences/Analytical chemistryPolymer chemistryElectrochemistryOrganometallic Compounds[CHIM.COOR]Chemical Sciences/Coordination chemistryReactivity (chemistry)Magnesium[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryHydrogen bondChemistryMagnesiumHydrogen Bonding[CHIM.MATE]Chemical Sciences/Material chemistry0104 chemical sciencesDicationCyclic voltammetryOxidation-ReductionDalton transactions (Cambridge, England : 2003)
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A Ser residue influences the structure and stability of a Pro-kinked transmembrane helix dimer

2012

AbstractWhen localized adjacent to a Pro-kink, Thr and Ser residues can form hydrogen bonds between their polar hydroxyl group and a backbone carbonyl oxygen and thereby modulate the actual bending angle of a distorted transmembrane α-helix. We have used the homo-dimeric transmembrane cytochrome b559′ to analyze the potential role of a highly conserved Ser residue for assembly and stabilization of transmembrane proteins. Mutation of the conserved Ser residue to Ala resulted in altered heme binding properties and in increased stability of the holo-protein, most likely by tolerating subtle structural rearrangements upon heme binding. The results suggest a crucial impact of an intrahelical Ser…

Models MolecularProlineHeme bindingStereochemistryDimerMolecular ConformationBiophysicsCofactor bindingHemeBiochemistryProtein Structure Secondarychemistry.chemical_compoundProtein structureProtein stabilitySerineProtein foldingCofactor bindingHydrogen bondCell MembranePhotosystem II Protein ComplexHydrogen BondingCell BiologyCytochrome b GroupTransmembrane proteinProtein Structure TertiaryOxygenTransmembrane domainHelix interactionchemistrySpectrophotometryMembrane proteinMutationTransmembrane helixProtein foldingDimerizationProtein BindingBiochimica et Biophysica Acta (BBA) - Biomembranes
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NMR Solution Structure of the Non-RGD Disintegrin Obtustatin

2003

The solution structure of obtustatin, a novel non-RGD disintegrin of 41 residues isolated from Vipera lebetina obtusa venom, and a potent and selective inhibitor of the adhesion of integrin alpha(1)beta(1) to collagen IV, has been determined by two-dimensional nuclear magnetic resonance. Almost the whole set of chemical shifts for 1H, 13C and 15N were assigned at natural abundance from 2D homonuclear and heteronuclear 500 MHz, 600 MHz and 800 MHz spectra at pH 3.0 recorded at 298 K and 303 K. Final structural constraints consisted of 302 non-redundant NOE (95 long-range, 60 medium, 91 sequential and 56 intra-residue), four disulfide bond distances, five chi1 dihedral angles and four hydroge…

Models MolecularProtein ConformationStereochemistryDisintegrinsMolecular Sequence DataStatic ElectricityViper VenomsDihedral angleCrystallography X-RayStructural BiologyDisintegrinAnimalsAmino Acid SequenceNuclear Magnetic Resonance BiomolecularMolecular BiologyProtein secondary structureConformational isomerismRGD motifMolecular StructureSequence Homology Amino AcidbiologyHydrogen bondChemistryCircular DichroismChemical shiftHydrogen BondingHydrogen-Ion ConcentrationSolutionsKineticsHeteronuclear moleculebiology.proteinOligopeptidesJournal of Molecular Biology
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Multiscale simulations of protein landscapes: Using coarse-grained models as reference potentials to full explicit models

2010

Evaluating the free-energy landscape of proteins and the corresponding functional aspects presents a major challenge for computer simulation approaches. This challenge is due to the complexity of the landscape and the enormous computer time needed for converging simulations. The use of simplified coarse-grained (CG) folding models offers an effective way of sampling the landscape but such a treatment, however, may not give the correct description of the effect of the actual protein residues. A general way around this problem that has been put forward in our early work (Fan et al., Theor Chem Acc 1999;103:77-80) uses the CG model as a reference potential for free-energy calculations of diffe…

Models MolecularProtein FoldingWork (thermodynamics)Protein ConformationChemistryMolecular Sequence DataStatic ElectricityProteinsSampling (statistics)Hydrogen BondingFolding (DSP implementation)Ph changesBiochemistryArticleStructure function correlationStructural BiologyKey (cryptography)Computer SimulationProtein foldingAmino Acid SequenceMolecular BiologyAlgorithmMathematicsSimulationEnergy (signal processing)Proteins: Structure, Function, and Bioinformatics
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The amorphous silica-liquid water interface studied by ab initio molecular dynamics (AIMD): local organization in global disorder

2014

International audience; The structural organization of water at a model of amorphous silica-liquid water interface is investigated by ab initio molecular dynamics (AIMD) simulations at room temperature. The amorphous surface is constructed with isolated, H-bonded vicinal and geminal silanols. In the absence of water, the silanols have orientations that depend on the local surface topology (i.e. presence of concave and convex zones). However, in the presence of liquid water, only the strong inter-silanol H-bonds are maintained, whereas the weaker ones are replaced by H-bonds formed with interfacial water molecules. All silanols are found to act as H- bond donors to water. The vicinal silanol…

Models MolecularProtonSurface Propertiesamorphous silicawatergeminal silanols02 engineering and technologyMolecular Dynamics Simulation010402 general chemistry01 natural sciencesAb initio molecular dynamicsComputational chemistryMoleculeGeneral Materials ScienceQuartzGeminalMolecular StructureChemistryab initio molecular dynamicsHydrogen Bonding[CHIM.MATE]Chemical Sciences/Material chemistrySilanes021001 nanoscience & nanotechnologyCondensed Matter PhysicsSilicon Dioxide0104 chemical sciencesAmorphous solidChemical physicsQuantum TheoryAmorphous silicaProtons0210 nano-technologyVicinal
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Computational study on hydrolysis of cefotaxime in gas phase and in aqueous solution

2012

We are presenting a theoretical study of the hydrolysis of a β-lactam antibiotic in gas phase and in aqueous solution by means of hybrid quantum mechanics/molecular mechanics potentials. After exploring the potential energy surfaces at semiempirical and density functional theory (DFT) level, potentials of mean force have been computed for the reaction in solution with hybrid PM3/TIP3P calculations and corrections with the B3LYP and M06-2X functionals. Inclusion of the full molecule of the antibiotic, Cefotaxime, in the gas phase molecular model has been demonstrated to be crucial since its carboxylate group can activate a nucleophilic water molecule. Moreover, the flexibility of the substra…

Models MolecularReaction mechanismPopulationCefotaximebeta-Lactamaseschemistry.chemical_compoundComputational chemistryMoleculeCarboxylateeducationConformational isomerismReaction mechanismeducation.field_of_studyAqueous solutionHydrolysisWaterHydrogen BondingGeneral ChemistryAnti-Bacterial AgentsSolutionsKineticsMetallo-beta-lactamasesComputational MathematicsModels ChemicalchemistryIntramolecular forceMβLsQuantum TheoryThermodynamicsDensity functional theoryGasesJournal of Computational Chemistry
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Fourfold [2]rotaxanes of calix[4]arenes by ring closure.

2006

Models MolecularRotaxanesChemistryStereochemistryClosure (topology)Hydrogen BondingGeneral ChemistryRing (chemistry)MetathesisCatalysisCyclizationPolymer chemistryCalixareneCalixarenesAngewandte Chemie (International ed. in English)
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