Search results for "Molecular Dynamic"

showing 10 items of 1090 documents

In situ structural analysis of SARS-CoV-2 spike reveals flexibility mediated by three hinges

2020

Flexible spikes The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein enables viral entry into host cells by binding to the angiotensin-converting enzyme 2 (ACE2) receptor and is a major target for neutralizing antibodies. About 20 to 40 spikes decorate the surface of virions. Turoňová et al. now show that the spike is flexibly connected to the viral surface by three hinges that are well protected by glycosylation sites. The flexibility imparted by these hinges may explain how multiple spikes act in concert to engage onto the flat surface of a host cell. Science, this issue p. 203

In situElectron Microscope TomographyGlycanGlycosylationFlexibility (anatomy)virusesProtein domainPneumonia ViralHingeMolecular Dynamics SimulationBiologylaw.inventionBetacoronavirusProtein DomainslawTarget identificationmedicineHumansPandemicsResearch ArticlesHost cell surfaceMultidisciplinarySARS-CoV-2R-ArticlesCryoelectron MicroscopyBiochemCOVID-19MicrobioResearch HighlightCell biologymedicine.anatomical_structureSpike Glycoprotein Coronavirusbiology.proteinRecombinant DNASpike (software development)Protein MultimerizationStructural biologyCoronavirus InfectionsResearch ArticleScience (New York, N.y.)
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Nanomechanical cleavage of molybdenum disulphide atomic layers.

2014

The discovery of two-dimensional materials became possible due to the mechanical cleavage technique. Despite its simplicity, the as-cleaved materials demonstrated surprising macrocontinuity, high crystalline quality and extraordinary mechanical and electrical properties that triggered global research interest. Here such cleavage processes and associated mechanical behaviours are investigated by a direct in situ transmission electron microscopy probing technique, using atomically thin molybdenum disulphide layers as a model material. Our technique demonstrates layer number selective cleavage, from a monolayer to double layer and up to 23 atomic layers. In situ observations combined with mole…

In situMultidisciplinaryMaterials scienceta114General Physics and Astronomychemistry.chemical_elementNanotechnologyCleavage (crystal)02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesGeneral Biochemistry Genetics and Molecular BiologySurface energy0104 chemical sciencesStrain energyMolecular dynamicschemistryMolybdenumHomogeneousChemical physicsMonolayer0210 nano-technologyNature communications
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Molecular modeling approaches in the discovery of new drugs for anti-cancer therapy: the investigation of p53-MDM2 interaction and its inhibition by …

2010

The mdm2 oncogene product, MDM2, is an ubiquitin protein ligase that inhibits the transcriptional activity of the tumor suppressor p53 and promotes its degradation. About 50% of all human cancers present mutations or deletions in the TP53 gene. In the remaining half of all human neoplasias that express the wild-type protein, aberrations of p53 regula- tors, such as MDM2, account for p53 inhibition. For this reason, designing small-molecule inhibitors of the p53-MDM2 protein-protein interaction is a promising strategy for the treatment of cancers retaining wild-type p53. The development of inhibitors has been challenging. Although many small-molecule MDM2 inhibitors have shown potent in vitr…

IndolesTumor suppressor geneAntineoplastic AgentsMolecular Dynamics SimulationBioinformaticsBiochemistryGene productNeoplasmsDrug DiscoverymedicineHumansImidazolinesMolecular Modeling New Drugs for Anti-Cancer Therapy p53-MDM2 InteractionPharmacologyBenzodiazepinonesbiologyOncogeneOrganic ChemistryCancerProto-Oncogene Proteins c-mdm2medicine.diseaseSettore CHIM/08 - Chimica FarmaceuticaSmall moleculeUbiquitin ligaseOxindolesProtein Structure TertiaryDrug Designbiology.proteinCancer researchMolecular MedicineMdm2PharmacophoreTumor Suppressor Protein p53Current medicinal chemistry
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Computational methodologies applied to Protein-Protein Interactions for molecular insights in Medicinal Chemistry

2021

In living systems, proteins usually team up into “molecular machinery” implementing several protein-to-protein physical contacts – or protein-protein interactions (PPIs) – to exert biological effects at both cellular and systems levels. Deregulations of protein-protein contacts have been associated with a huge number of diseases in a wide range of medical areas, such as oncology, cancer immunotherapy, infectious diseases, neurological disorders, heart failure, inflammation and oxidative stress. PPIs are very complex and usually characterised by specific shape, size and complementarity. The protein interfaces are generally large, broad and shallow, and frequently protein-protein contacts are…

InflammationComputer-Aided Drug DesignMolecular DynamicFactor HMolecular ModelingCOVID-19ACE2MUC1SpikeDrug AddictionHOXComputational Alanine ScanningC3bSettore CHIM/08 - Chimica FarmaceuticaProtein-Protein InteractionMolecular DockingComputational ChemistryNLRP3PBXCIN85RasGRF1RaCancer
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Vibrational Sum Frequency Generation Spectroscopy of the Water Liquid–Vapor Interface from Density Functional Theory-Based Molecular Dynamics Simulat…

2013

International audience; The vibrational sum frequency generation (VSFG) spectrum of the water liquid-vapor (LV) interface is calculated using density functional theory-based molecular dynamics simulations. The real and imaginary parts of the spectrum are in good agreement with the experimental data, and we provide an assignment of the SFG bands according to the dipole orientation of the interfacial water molecules. We use an instantaneous definition of the surface, which is more adapted to the study of interfacial phenomena than the Gibbs dividing surface. By calculating the vibrational (infrared, Raman) properties for interfaces of varying thickness, we show that the bulk spectra signature…

InfraredBulk spectra02 engineering and technologyMolecular dynamicsVibrational sum-frequency generations010402 general chemistry01 natural sciencesMolecular physicsSpectral lineInterfacial phenomenaLiquid-vapor interfaceMolecular dynamicssymbols.namesakeDipole orientationComputational chemistryGeneral Materials SciencePhysical and Theoretical ChemistryDividing surfacesDensity functionalsSum-frequency generationMolecular dynamics simulationsChemistryInterfacial water moleculesThin layers021001 nanoscience & nanotechnologyLiquid-vapor0104 chemical sciencesDipoleImaginary partsDensity functional theoryVaporssymbolsDensity functional theory[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]0210 nano-technologyRaman spectroscopyVarying thicknessSum frequency generation spectroscopyThe Journal of Physical Chemistry Letters
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Dithiametacyclophane mit Dreifachbindungen

1994

Dithiametacyclophanes with Triple Bonds Schemes 1 and 2 show the syntheses of dithia[8]metacyclo-phanes 4a-d and tetrathia[m.n]metacyclophanes 9, 10 by cyclization reactions applying the cesium effect. All these cyclophanes contain C—C triple bonds which influence the molecular dynamics; especially the halogen substituents in 4b-d obstruct the topomerization.

Inorganic ChemistryMolecular dynamicschemistry.chemical_compoundThioureaChemistryHalogenTriple bondm-XylenePhotochemistryMedicinal chemistryCyclophaneChemische Berichte
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MMGBSA As a Tool To Understand the Binding Affinities of Filamin–Peptide Interactions

2013

Filamins (FLN) are large dimeric proteins that cross-link actin and work as important scaffolds in human cells. FLNs consist of an N-terminal actin-binding domain followed by 24 immunoglobulin-like domains (FLN1-24). FLN domains are divided into four subgroups based on their amino acid sequences. One of these subgroups, including domains 4, 9, 12, 17, 19, 21, and 23, shares a similar ligand-binding site between the β strands C and D. Several proteins, such as integrins β2 and β7, glycoprotein Ibα (GPIbα), and migfilin, have been shown to bind to this site. Here, we computationally estimated the binding free energies of filamin A (FLNa) subunits with bound peptides using the molecular mechan…

Integrin beta ChainsFilaminsGeneral Chemical EngineeringIntegrinPeptidePlasma protein bindingMolecular Dynamics SimulationLibrary and Information SciencesBiologyLigandsFilaminta3111Protein Structure SecondaryProtein structureProtein Interaction MappingHumansFLNAProtein Interaction Domains and MotifsBinding siteta116chemistry.chemical_classificationBinding Sitesta1182General ChemistryComputer Science ApplicationsAmino acidCytoskeletal ProteinsCrystallographyPlatelet Glycoprotein GPIb-IX ComplexchemistryCD18 AntigensBiophysicsbiology.proteinThermodynamicsPeptidesCell Adhesion MoleculesAlgorithmsProtein BindingJournal of Chemical Information and Modeling
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Tracking Ca

2019

We characterize thus-far elusive domain rearrangements of a calcium-transporting ATPase in the native membrane.

Ion TransportProtein ConformationBiophysicsQuantitative Structure-Activity RelationshipSciAdv r-articlesMolecular Dynamics SimulationCrystallography X-RaySarcoplasmic Reticulum Calcium-Transporting ATPasesKineticsStructural BiologyCalciumProtein Interaction Domains and MotifsResearch ArticlesProtein BindingResearch ArticleScience advances
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Mesoscopic organization in ionic liquids.

2017

We discuss some published results and provide new observations concerning the high level of structural complexity that lies behind the nanoscale correlations in ionic liquids (ILs) and their mixtures with molecular liquids. It turns out that this organization is a consequence of the hierarchical construction on both spatial (from ångström to several nanometer) and temporal (from fraction of picosecond to hundreds of nanosecond) scales, which requires joint use of experimental and computational tools. © 2017, Springer International Publishing Switzerland.

Ionic LiquidsNanotechnology02 engineering and technologyIonic liquidMolecular Dynamics Simulation010402 general chemistry01 natural sciencesMesoscopic and microscopic structurechemistry.chemical_compoundMolecular dynamicsX-ray and neutron scattering;Molecular dynamics simulation;Ionic liquid;Mesoscopic and microscopic structureAngstromNanoscopic scaleMesoscopic physicsChemistry (all)X-ray and neutron scatteringGeneral ChemistryNanosecond021001 nanoscience & nanotechnology0104 chemical sciencesIonic liquid; Mesoscopic and microscopic structure; Molecular dynamics simulation; X-ray and neutron scattering.chemistryChemical physicsPicosecondIonic liquid0210 nano-technologyTopics in current chemistry (Cham)
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Mesoscopic structural organization in triphilic room temperature ionic liquids

2013

Room temperature ionic liquids are one of the most exciting classes of materials in the last decade. The interest for these low melting, ionic compounds stems from both their technological impact and the stimulating plethora of structural and dynamic peculiarities in the mesoscopic space-time scales. It is nowadays well-established that they are characterised by an enhanced degree of mesoscopic order originating from their inherent amphiphilicity. In this contribution we highlight the existence of a further degree of mesoscopic complexity when dealing with RTILs bearing a medium length fluorous tail: such triphilic materials (they simultaneously contain polar, hydrophobic and fluorophilic m…

Ionic liquids StructureMesoscopic physicsStructural organizationethylammonium; molecular dynamics; 1-ethyl-3-methylimidazoliumIonic bondingNanotechnology02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology1-ethyl-3-methylimidazolium01 natural sciencesmolecular dynamics0104 chemical scienceschemistry.chemical_compoundethylammoniumchemistryIonic liquidTechnological impactPhysical and Theoretical Chemistry0210 nano-technologySmart applications
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