Search results for "molecular dynamics simulation"

showing 10 items of 260 documents

Proposal of a Computational Approach for Simulating Thermal Bosonic Fields in Phase Space

2019

When a quantum field is in contact with a thermal bath, the vacuum state of the field may be generalized to a thermal vacuum state, which takes into account the thermal noise. In thermo field dynamics, this is realized by doubling the dimensionality of the Fock space of the system. Interestingly, the representation of thermal noise by means of an augmented space is also found in a distinctly different approach based on the Wigner transform of both the field operators and density matrix, which we pursue here. Specifically, the thermal noise is introduced by augmenting the classical-like Wigner phase space by means of Nos&eacute

PhysicsDensity matrixQuantum PhysicsField (physics)Vacuum statebosonic fieldFOS: Physical sciencesFock spacemolecular dynamics simulationPhase spaceBosonic fieldWigner distribution functionWigner functionStatistical physicsQuantum field theoryWigner function bosonic field temperature control molecular dynamics simulationQuantum Physics (quant-ph)temperature controlPhysics
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Fractional-order theory of heat transport in rigid bodies

2014

Abstract The non-local model of heat transfer, used to describe the deviations of the temperature field from the well-known prediction of Fourier/Cattaneo models experienced in complex media, is framed in the context of fractional-order calculus. It has been assumed (Borino et al., 2011 [53] , Mongiovi and Zingales, 2013 [54] ) that thermal energy transport is due to two phenomena: ( i ) A short-range heat flux ruled by a local transport equation; ( ii ) A long-range thermal energy transfer proportional to a distance-decaying function, to the relative temperature and to the product of the interacting masses. The distance-decaying function is assumed in the functional class of the power-law …

PhysicsNumerical AnalysisField (physics)business.industryApplied MathematicsFractional derivatives; Fractional-order calculus; Fractional-order derivatives; Generalized entropies; Molecular dynamics simulations; Nonlocal; Relative temperatures; Thermal energy transportThermodynamicsContext (language use)Fractional derivativeFractional-order calculuFractional calculusRelative temperatureHeat fluxModeling and SimulationHeat transferGeneralized entropieMolecular dynamics simulationFractional-order derivativeBoundary value problembusinessConvection–diffusion equationNonlocalSettore ICAR/08 - Scienza Delle CostruzioniThermal energyThermal energy transport
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The Internal Dynamics of Fibrinogen and Its Implications for Coagulation and Adsorption

2015

Fibrinogen is a serum multi-chain protein which, when activated, aggregates to form fibrin, one of the main components of a blood clot. Fibrinolysis controls blood clot dissolution through the action of the enzyme plasmin, which cleaves fibrin at specific locations. Although the main biochemical factors involved in fibrin formation and lysis have been identified, a clear mechanistic picture of how these processes take place is not available yet. This picture would be instrumental, for example, for the design of improved thrombolytic or anti-haemorrhagic strategies, as well as, materials with improved biocompatibility. Here, we present extensive molecular dynamics simulations of fibrinogen w…

Plasminmedicine.medical_treatmentAllosteric regulationPlasma protein bindingMolecular Dynamics SimulationFibrinogenFibrinCellular and Molecular NeuroscienceFibrinolysisGeneticsmedicineHumanslcsh:QH301-705.5Molecular BiologyBlood CoagulationEcology Evolution Behavior and SystematicsIntegrin bindingEcologybiologyChemistryComputational BiologyFibrinogenlcsh:Biology (General)Computational Theory and MathematicsCoagulationBiochemistryModeling and Simulationbiology.proteinAdsorptionmedicine.drugResearch ArticleProtein BindingPLoS Computational Biology
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Bioinspired catechol-terminated self-assembled monolayers with enhanced adhesion properties

2013

The role of the catechol moiety in the adhesive properties of mussel proteins and related synthetic materials has been extensively studied in the last years but still remains elusive. Here, a simplified model approach is presented based on a self-assembled monolayer (SAM) of upward-facing catechols thiol-bound to epitaxial gold substrates. The orientation of the catechol moieties is confirmed by spectroscopy, which also showed lack of significant amounts of interfering o-quinones. Local force-distance curves on the SAM measured by atomic force microscopy (AFM) shows an average adhesion force of 45 nN, stronger than that of a reference polydopamine coating, along with higher reproducibility …

PolydopamineIndolesPolymersCatecholsBiocompatible MaterialsNanotechnologyMolecular Dynamics Simulationengineering.materialBiomimèticaMicroscopy Atomic ForceBiomaterialsMolecular dynamicschemistry.chemical_compound:Enginyeria química [Àrees temàtiques de la UPC]Coated Materials BiocompatibleCoatingMonolayerMoietyGeneral Materials ScienceMagnetite NanoparticlesAdhesive surfaceCatecholChemistrySAMsAdhesivenessSelf-assembled monolayerGeneral ChemistryAdhesionBiomimetic polymersChemical engineeringCatecholengineeringPrintingMagnetic nanoparticlesBiomimeticGoldBiotechnology
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Conformations, Transverse Fluctuations and Crossover Dynamics of a Semi-Flexible Chain in Two Dimensions

2014

We present a unified scaling description for the dynamics of monomers of a semiflexible chain under good solvent condition in the free draining limit. We consider both the cases where the contour length $L$ is comparable to the persistence length $\ell_p$ and the case $L\gg \ell_p$. Our theory captures the early time monomer dynamics of a stiff chain characterized by $t^{3/4}$ dependence for the mean square displacement(MSD) of the monomers, but predicts a first crossover to the Rouse regime of $t^{2\nu/{1+2\nu}}$ for $\tau_1 \sim \ell_p^3$, and a second crossover to the purely diffusive dynamics for the entire chain at $\tau_2 \sim L^{5/2}$. We confirm the predictions of this scaling descr…

PolymersCrossoverMolecular ConformationGeneral Physics and AstronomyFOS: Physical sciencesMolecular Dynamics SimulationCondensed Matter - Soft Condensed MatterChain (algebraic topology)Statistical physicsPhysics - Biological PhysicsPhysical and Theoretical ChemistryScalingBrownian motionPhysicsPersistence lengthQuantitative Biology::BiomoleculesMathematics::Functional AnalysisModels TheoreticalSolutionsCondensed Matter::Soft Condensed MatterMean squared displacementLennard-Jones potentialBiological Physics (physics.bio-ph)SolventsBrownian dynamicsSoft Condensed Matter (cond-mat.soft)
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A Monte Carlo Study of Knots in Long Double-Stranded DNA Chains.

2016

We determine knotting probabilities and typical sizes of knots in double-stranded DNA for chains of up to half a million base pairs with computer simulations of a coarse-grained bead-stick model: Single trefoil knots and composite knots which include at least one trefoil as a prime factor are shown to be common in DNA chains exceeding 250,000 base pairs, assuming physiologically relevant salt conditions. The analysis is motivated by the emergence of DNA nanopore sequencing technology, as knots are a potential cause of erroneous nucleotide reads in nanopore sequencing devices and may severely limit read lengths in the foreseeable future. Even though our coarse-grained model is only based on …

PolymersMaterials by StructureMolecular biologyMaterials ScienceElectrophoretic techniquesDNA electrophoresisNucleotide SequencingMolecular Dynamics SimulationBiochemistryNanoporesSequencing techniquesMathematical and Statistical Techniquesstomatognathic systemGeneticsBiochemical SimulationsNanotechnologyDNA sequencingMaterials by AttributeNanomaterialsQuantitative Biology::BiomoleculesBiology and life sciencesMathematical Modelsfood and beveragesComputational BiologyDNAPolymer ChemistryMathematics::Geometric TopologyResearch and analysis methodsNucleic acidsChemistrysurgical procedures operativeMolecular biology techniquesMacromoleculesRandom WalkPhysical SciencesNucleic Acid ConformationEngineering and TechnologyMonte Carlo MethodResearch ArticlePLoS computational biology
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A lipocentric view of peptide-induced pores

2010

Although lipid membranes serve as effective sealing barriers for the passage of most polar solutes, nonmediated leakage is not completely improbable. A high activation energy normally keeps unassisted bilayer permeation at a very low frequency, but lipids are able to self-organize as pores even in peptide-free and protein-free membranes. The probability of leakage phenomena increases under conditions such as phase coexistence, external stress or perturbation associated to binding of nonlipidic molecules. Here, we argue that pore formation can be viewed as an intrinsic property of lipid bilayers, with strong similarities in the structure and mechanism between pores formed with participation …

Pore Forming Cytotoxic ProteinsCell Membrane PermeabilityMembrane permeabilityMembrane lipidsPore energeticsBiophysicsThermal fluctuationsReviewMolecular Dynamics SimulationSurface tensionMembrane LipidsAnti-Infective AgentsLipid bilayerChemistryBilayerLipidic poreGeneral MedicinePermeationCrystallographyMembrane permeabilityMembraneBiophysicsAntimicrobial peptidePore structurePorosityPore-forming proteinsEuropean Biophysics Journal
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Immunoproteasome and Non-Covalent Inhibition: Exploration by Advanced Molecular Dynamics and Docking Methods

2021

The selective inhibition of immunoproteasome is a valuable strategy to treat autoimmune, inflammatory diseases, and hematologic malignancies. Recently, a new series of amide derivatives as non-covalent inhibitors of the β1i subunit with Ki values in the low/submicromolar ranges have been identified. Here, we investigated the binding mechanism of the most potent and selective inhibitor, N-benzyl-2-(2-oxopyridin-1(2H)-yl)propanamide (1), to elucidate the steps from the ligand entrance into the binding pocket to the ligand-induced conformational changes. We carried out a total of 400 ns of MD-binding analyses, followed by 200 ns of plain MD. The trajectories clustering allowed identifying thre…

Proteasome Endopeptidase ComplexStereochemistryPharmaceutical ScienceOrganic chemistryinduced-fit dockingMolecular Dynamics Simulation01 natural sciencesArticlemetadynamicsAnalytical Chemistry03 medical and health scienceschemistry.chemical_compoundimmunoproteasomeQD241-441AmideDrug DiscoveryOrganosilicon CompoundsPhysical and Theoretical Chemistrynon-covalent inhibitor030304 developmental biology0303 health sciencesBinding Sites010405 organic chemistrymolecular dynamicnon-covalent inhibitorsMetadynamicsRational designDipeptidesLigand (biochemistry)PropanamideSettore CHIM/08 - Chimica Farmaceuticamolecular dynamics0104 chemical sciencesMolecular Docking SimulationchemistryChemistry (miscellaneous)Docking (molecular)MD bindingMolecular MedicinemetadynamicLead compoundOligopeptidesProteasome InhibitorsAcetamideProtein BindingMolecules
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Kinetic analysis and molecular modeling of the inhibition mechanism of roneparstat (SST0001) on human heparanase

2016

Heparanase is a β-d-glucuronidase which cleaves heparan sulfate chains in the extracellular matrix and on cellular membranes. A dysregulated heparanase activity is intimately associated with cell invasion, tumor metastasis and angiogenesis, making heparanase an attractive target for the development of anticancer therapies. SST0001 (roneparstat; Sigma-Tau Research Switzerland S.A.) is a non-anticoagulant 100% N-acetylated and glycol-split heparin acting as a potent heparanase inhibitor, currently in phase I in advanced multiple myeloma. Herein, the kinetics of heparanase inhibition by roneparstat is reported. The analysis of dose-inhibition curves confirmed the high potency of roneparstat (I…

Protein Conformation alpha-Helical0301 basic medicineSST0001Molecular modelhomology modelingAmino Acid MotifsPlasma protein bindingMolecular Dynamics SimulationBiochemistryMolecular Docking SimulationheparanaseSubstrate Specificity03 medical and health scienceschemistry.chemical_compound0302 clinical medicinePolysaccharidesHumansProtein Interaction Domains and MotifsHeparanaseHomology modelingEnzyme InhibitorsGlucuronidaseBinding Siteskinetic inhibition analysisHeparinComputational BiologyHeparan sulfateRecombinant ProteinsAcidobacteriaMolecular Docking SimulationEnzyme bindingKinetics030104 developmental biologyCarbohydrate SequenceFondaparinuxchemistryBiochemistryStructural Homology ProteinDocking (molecular)030220 oncology & carcinogenesisBiophysicsroneparstatThermodynamicsProtein Conformation beta-StrandORIGINAL ARTICLESProtein BindingGlycobiology
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A potential solution to avoid overdose of mixed drugs in the event of Covid-19: Nanomedicine at the heart of the Covid-19 pandemic.

2021

Since 2020, the world is facing the first global pandemic of 21st century. Among all the solutions proposed to treat this new strain of coronavirus, named SARS-CoV-2, the vaccine seems a promising way but the delays are too long to be implemented quickly. In the emergency, a dual therapy has shown its effectiveness but has also provoked a set of debates around the dangerousness of a particular molecule, hydroxychloroquine. In particular, the doses to be delivered, according to the studies, were well beyond the acceptable doses to support the treatment without side effects. We propose here to use all the advantages of nanovectorization to address this question of concentration. Using quantum…

Protein Conformation alpha-HelicalComputer science02 engineering and technologyAzithromycinDrug Delivery SystemsPandemicMaterials ChemistryDrug Dosage CalculationsSpectroscopymedia_common0303 health sciencesEvent (computing)021001 nanoscience & nanotechnologyComputer Graphics and Computer-Aided DesignMolecular Docking SimulationNanomedicineRisk analysis (engineering)Spike Glycoprotein CoronavirusDensity functional theory calculationsNanomedicineThermodynamicsNitrogen OxidesAngiotensin-Converting Enzyme 20210 nano-technologyHydroxychloroquineProtein BindingDrugBoron CompoundsCoronavirus disease 2019 (COVID-19)media_common.quotation_subjectSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2)Molecular Dynamics SimulationAntiviral AgentsArticle03 medical and health sciencesHumansProtein Interaction Domains and MotifsDual therapyPhysical and Theoretical Chemistry030304 developmental biologyDrug transportBinding SitesSARS-CoV-2Molecular dynamics simulationsCOVID-19NanostructuresCOVID-19 Drug TreatmentKineticsQuantum TheoryProtein Conformation beta-StrandNanovectorizationJournal of molecular graphicsmodelling
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