Search results for " molecular dynamics"

showing 10 items of 126 documents

Structure, stability, and fragmentation of sodium bis(2-ethylhexyl)sulfosuccinate negatively charged aggregates in vacuo by MD simulations.

2014

Negatively charged supramolecular aggregates formed in vacuo by n bis(2-ethylhexyl)sulfosuccinate (AOT(-)) anions and n + n(c) sodium counterions (i.e., [AOT(n) Na(n+nc)](nc)) have been investigated by molecular dynamics (MD) simulations for n = 1 to 20 and n(c) = -1 to -5. By comparing the maximum excess charge values of negatively and positively charged AOTNa aggregates, it is found that the charge storage capability is higher for the latter systems, the difference decreasing as the aggregation number increases. Statistical analysis of physical properties like gyration radii and moment of inertia tensors of aggregates provides detailed information on their structural properties. Even for …

SodiumSupramolecular chemistryMolecular Conformationchemistry.chemical_elementFragmentation patternsMolecular Dynamics SimulationAOTNa Self-assembling Charged reverse micelles Molecular dynamics simulation (MD) Supramolecular aggregates in vacuo Fragmentation patternsMicelleMolecular dynamicsSurface-Active AgentsPulmonary surfactantStructural BiologyAotNa; self-assembling; charged revrse micelle; Molecular Dynamics simulations; Supramolecular aggregates in vacuo; Fragmentation patternsSpectroscopyAlkylMicellesSettore CHIM/02 - Chimica Fisicachemistry.chemical_classificationIonsDioctyl Sulfosuccinic AcidAggregation numberAotNacharged revrse micelleself-assemblingSupramolecular aggregates in vacuoCrystallographychemistryThermodynamicsMolecular Dynamics simulationsCounterionJournal of the American Society for Mass Spectrometry
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Tuning active Brownian motion with shot noise energy pulses

2009

The main aim of this work is to explore the possibility of modeling the biological energy support mediated by absorption of ATP (adenosine triphosphate) as an energetic shot noise. We develop a general model with discrete input of energy pulses and study shot-noise-driven ratchets. We consider these ratchets as prototypes of Brownian motors driven by energy-rich ATP molecules. Our model is a stochastic machine able to acquire energy from the environment and convert it into kinetic energy of motion. We present characteristic features and demonstrate the possibility of tuning these motors by adapting the mean frequency of the discrete energy inputs, which are described as a special shot noise…

Statistics and ProbabilityPhysicsPhysics::Biological PhysicsWork (thermodynamics)driven diffusive systems (theory) stochastic particle dynamics (theory) molecular motors (theory) molecular dynamics BRonian motion Fluctuation phenomenaShot noiseStatistical and Nonlinear PhysicsKinetic energyBrownian motorQuantitative Biology::Subcellular ProcessesClassical mechanicsMolecular motorStatistical physicsStatistics Probability and UncertaintyAbsorption (electromagnetic radiation)Energy (signal processing)Brownian motion
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In Silico Design, Synthesis and Biological Evaluation of Anticancer Arylsulfonamide Endowed with Anti-Telomerase Activity

2022

Telomerase, a reverse transcriptase enzyme involved in DNA synthesis, has a tangible role in tumor progression. Several studies have evidenced telomerase as a promising target for developing cancer therapeutics. The main reason is due to the overexpression of telomerase in cancer cells (85–90%) compared with normal cells where it is almost unexpressed. In this paper, we used a structure-based approach to design potential inhibitors of the telomerase active site. The MYSHAPE (Molecular dYnamics SHared PharmacophorE) approach and docking were used to screen an in-house library of 126 arylsulfonamide derivatives. Promising compounds were synthesized using classical and green methods. Com…

SulfonamidesRPharmaceutical ScienceAnticancer compounds; Arylsulfonamide; Docking; Molecular dynamics; Pharmacophore modeling; Structure-based drug design; Sulfonamides; Telomerase inhibitorsMolecular dynamicsSettore CHIM/08 - Chimica FarmaceuticaArticleDockingRS1-441Anticancer compoundsTelomerase inhibitorsPharmacy and materia medicaDrug DiscoveryArylsulfonamideMedicineMolecular Medicinesulfonamides; arylsulfonamide; anticancer compounds; telomerase inhibitors; structure-based drug design; pharmacophore modeling; docking; molecular dynamicsStructure-based drug designPharmacophore modeling
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A Stereochemically Driven Supramolecular Polymerisation

2018

Anthracyclines self-assemble in water into dimers. In the presence of sufficiently high salt (NaCl) concentrations, solutions of the antibiotic doxorubicin, but not those of the closely related molecules daunomycin and epirubicin, turn into gels barely compatible with the presence of small oligomers. The use of spectroscopic, scattering, imaging and computational techniques, allowed light to be shed on the self-assembly process that triggered doxorubicin gelification. A complex picture emerged, with doxorubicin molecules assembled into long, highly chiral, supramolecular aggregates made of hundreds of units, showing redshifted fluorescence spectra, very short fluorescence lifetimes and smal…

Supramolecular chemistry02 engineering and technology010402 general chemistryPhotochemistrydoxorubicin01 natural sciencesCatalysisTurn (biochemistry)chemistry.chemical_compoundMolecular dynamicsanthracyclines; doxorubicin; fluorescence; circular dichroism; SAXS; molecular dynamicsMoleculeanthracyclinesScatteringOrganic ChemistrySAXSGeneral Chemistry021001 nanoscience & nanotechnologyFluorescencemolecular dynamicscircular dichroism0104 chemical sciencesMonomerchemistryPolymerizationfluorescence0210 nano-technologyChemistry - A European Journal
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Study of High-Temperature Behaviour of ZnO by Ab Initio Molecular Dynamics Simulations and X-ray Absorption Spectroscopy

2021

Wurtzite-type zinc oxide (w-ZnO) is a widely used material with a pronounced structural anisotropy along the c axis, which affects its lattice dynamics and represents a difficulty for its accurate description using classical models of interatomic interactions. In this study, ab initio molecular dynamics (AIMD) was employed to simulate a bulk w-ZnO phase in the NpT ensemble in the high-temperature range from 300 K to 1200 K. The results of the simulations were validated by comparison with the experimental Zn K-edge extended X-ray absorption fine structure (EXAFS) spectra and known diffraction data. AIMD NpT simulations reproduced well the thermal expansion of the lattice, and the pronounced …

TechnologyMaterials science02 engineering and technology01 natural sciencesMolecular physicsThermal expansionArticleCondensed Matter::Materials Science0103 physical sciencesAtomGeneral Materials Science010306 general physicsAnisotropyAbsorption (electromagnetic radiation)MicroscopyQC120-168.85X-ray absorption spectroscopyExtended X-ray absorption fine structureTab initio molecular dynamicsQH201-278.5Anharmonicityzinc oxideEngineering (General). Civil engineering (General)021001 nanoscience & nanotechnologyTK1-9971Molecular geometryDescriptive and experimental mechanicsZnOElectrical engineering. Electronics. Nuclear engineeringTA1-20400210 nano-technologyextended X-ray absorption fine structureMaterials
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Atypical titration curves for GaAl12Keggin-ions explained by a joint experimental and simulation approach

2018

Although they have been widely used as models for oxide surfaces, the deprotonation behaviors of the Keggin-ions (MeAl127+) and typical oxide surfaces are very different. On Keggin-ions, the deprotonation occurs over a very narrow pH range at odds with the broad charging curve of larger oxide surfaces. Depending on the Me concentration, the deprotonation curve levels off sooner (high Me concentration) or later (for low Me concentration). The leveling off shows the onset of aggregation before which the Keggin-ions are present as individual units. We show that the atypical titration data previously observed for some GaAl12 solutions in comparison to the originally reported data can be explain…

Titration curveAnalytical chemistryOxideGeneral Physics and Astronomy02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesIonAb initio molecular dynamicschemistry.chemical_compoundDeprotonationchemistryOctahedronTitrationPhysical and Theoretical Chemistry0210 nano-technologyJoint (geology)The Journal of Chemical Physics
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TOWARD ENRICHED VHTS FOR CDK2 INHIBITORS: MOLECULAR DYNAMICS, PHARMACOPHORE MODELLING, AND DOCKING

2019

Cyclin-Dependent Kinases-2 (CDK2) are members of the serine/threonine protein kinases family. They play an important role in the regulation events of the eukaryotic cell division cycle, especially during the G1 to S phase transition. Experimental evidence indicates that excessive expression of CDK2s should cause abnormal cell cycle regulation. Therefore, since a long time, CDK2s have been considered potential therapeutic targets for cancer therapy. In this work, we collected one-hundred and forty-nine complexes of inhibitors bound in the CDK2-ATP pocket submitting to short MD simulations (10ns) and free energy calculation by means of MM-GBSA. The calculate ∆G values have been compared with …

VHTS CDK2 INHIBITORS MOLECULAR DYNAMICS PHARMACOPHORE MODELLING DOCKING
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Correction: “On-the-fly” coupled cluster path-integral molecular dynamics: impact of nuclear quantum effects on the protonated water dimer

2015

We present an accelerated ab initio path-integral molecular dynamics technique, where the interatomic forces are calculated “on-the-fly” by accurate coupled cluster electronic structure calculations. In this way not only dynamic electron correlation, but also the harmonic and anharmonic zero-point energy, as well as tunneling effects are explicitly taken into account. This method thus allows for very precise finite temperature quantum molecular dynamics simulations. The predictive power of this novel approach is illustrated on the example of the protonated water dimer, where the impact of nuclear quantum effects on its structure and the 1H magnetic shielding tensor are discussed in detail.

Water dimerElectronic correlationChemistryAb initioGeneral Physics and AstronomyElectronic structureMolecular physicsMolecular dynamicsCoupled clusterQuantum mechanicsPath integral molecular dynamicsPhysical and Theoretical ChemistryAtomic physicsQuantum tunnellingPhysical Chemistry Chemical Physics
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Iron’s Wake: The Performance of Quantum Mechanical-Derived Versus General-Purpose Force Fields Tested on a Luminescent Iron Complex

2020

Recently synthetized iron complexes have achieved long-lived excited states and stabilities which are comparable, or even superior, to their ruthenium analogues, thus representing an eco-friendly and cheaper alternative to those materials based on rare metals. Most of computational tools which could help unravel the origin of this large efficiency rely on ab-initio methods which are not able, however, to capture the nanosecond time scale underlying these photophysical processes and the influence of their realistic environment. Therefore, it exists an urgent need of developing new low-cost, but still accurate enough, computational methodologies capable to deal with the steady-state and trans…

Work (thermodynamics)AcetonitrilesLuminescenceIronPharmaceutical ScienceMolecular Dynamics Simulation010402 general chemistry01 natural sciencesArticleAnalytical Chemistrylcsh:QD241-441Molecular dynamicschemical environmentlcsh:Organic chemistry0103 physical sciencesDrug Discoverytime-dependent density functional theory.Statistical physicsPhysical and Theoretical ChemistryQuantumComputingMilieux_MISCELLANEOUSPhysics010304 chemical physicsSpectrum AnalysisScale (chemistry)Organic ChemistryTime-dependent density functional theoryNanosecond0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrytime-dependent density functional theoryiron complexChemistry (miscellaneous)Excited stateSolventsQuantum TheoryMolecular MedicineLuminescenceIron Compoundsforce field molecular dynamicsMolecules
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Targeting G-quadruplexes with Organic Dyes: Chelerythrine–DNA Binding Elucidated by Combining Molecular Modeling and Optical Spectroscopy

2019

The DNA-binding of the natural benzophenanthridine alkaloid chelerythrine (CHE) has been assessed by combining molecular modeling and optical absorption spectroscopy. Specifically, both double-helical (B-DNA) and G-quadruplex sequences&mdash

anticancer drugslcsh:Therapeutics. PharmacologySettore CHIM/03 - Chimica Generale E Inorganicalcsh:RM1-950All atom molecular dynamicall atom molecular dynamics[CHIM]Chemical Sciencesheterocyclic compoundsAnticancer drugguanine quadruplexesArticleComputingMilieux_MISCELLANEOUScircular dichroism
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