Search results for "Computer Science Applications"

showing 10 items of 3993 documents

Computational analysis of lung deformation after murine pneumonectomy. [corrected].

2012

In many mammalian species, the removal of one lung (pneumonectomy) is associated with the compensatory growth of the remaining lung. To investigate the hypothesis that parenchymal deformation may trigger lung regeneration, we used microCT scanning to create 3-dimensional finite element geometric models of the murine lung pre- and post-pneumonectomy (24 hours). The structural correspondence between models was established using anatomic landmarks and an iterative computational algorithm. When compared with the pre-pneumonectomy lung, the post-pneumonectomy models demonstrated significant translation and rotation of the cardiac lobe into the post-pneumonectomy pleural space. 2-dimensional maps…

Models AnatomicPathologymedicine.medical_specialtyX-ray microtomographymedicine.medical_treatmentFinite Element AnalysisBiomedical EngineeringCompensatory growth (organ)BioengineeringBiologyDeformation (meteorology)ArticlePneumonectomyMiceParenchymamedicineAnimalsRegenerationComputational analysisPneumonectomyLungLungGeneral MedicineAnatomyX-Ray Microtomographyrespiratory systemLoberespiratory tract diseasesComputer Science ApplicationsHuman-Computer InteractionMice Inbred C57BLmedicine.anatomical_structureComputer methods in biomechanics and biomedical engineering
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Isolation and Characterization of Two Klebsiella pneumoniae Phages Encoding Divergent Depolymerases

2020

The emergence of multidrug-resistant bacteria is a major global health concern. The search for new therapies has brought bacteriophages into the spotlight, and new phages are being described as possible therapeutic agents. Among the bacteria that are most extensively resistant to current antibiotics is Klebsiella pneumoniae, whose hypervariable extracellular capsule makes treatment particularly difficult. Here, we describe two new K. pneumoniae phages, &pi

Models Molecular0301 basic medicineKlebsiellaPhage therapyKlebsiella pneumoniae<i>Klebsiella pneumoniae</i>virusesmedicine.medical_treatmentAntibioticsMolecular Conformationlcsh:ChemistryBacteriophagebacteriophagewide infection rangeBacteriophagesAntigens Virallcsh:QH301-705.5PhylogenySpectroscopybiologyGeneral Medicine3. Good healthComputer Science ApplicationsKlebsiella pneumoniaePhenotypephage therapyPhage therapymedicine.drug_class030106 microbiologyGenome ViralArticleHost SpecificityCatalysisMicrobiologyInorganic ChemistryViral Proteins03 medical and health sciencesPodoviridaeBacteriolysismedicineAmino Acid SequencePhysical and Theoretical ChemistryBacteriophageMolecular BiologyTropismWhole Genome SequencingOrganic ChemistryComputational BiologyGenetic VariationMolecular Sequence Annotationbiology.organism_classificationKlebsiella Infections030104 developmental biologylcsh:Biology (General)lcsh:QD1-999Wide infection rangeBacteriaInternational Journal of Molecular Sciences
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Metallothionein Gene Family in the Sea Urchin Paracentrotus lividus: Gene Structure, Differential Expression and Phylogenetic Analysis

2017

Metallothioneins (MT) are small and cysteine-rich proteins that bind metal ions such as zinc, copper, cadmium, and nickel. In order to shed some light on MT gene structure and evolution, we cloned seven Paracentrotus lividus MT genes, comparing them to Echinodermata and Chordata genes. Moreover, we performed a phylogenetic analysis of 32 MTs from different classes of echinoderms and 13 MTs from the most ancient chordates, highlighting the relationships between them. Since MTs have multiple roles in the cells, we performed RT-qPCR and in situ hybridization experiments to understand better MT functions in sea urchin embryos. Results showed that the expression of MTs is regulated throughout de…

Models Molecular0301 basic medicineProtein Conformationmetallothionein; multigene families; evolution; metal; echinoderms; embryonic development; gene expressionCatalysiGene OrderMetallothioneinSea urchinPhylogenySpectroscopyPhylogenetic treebiologyEchinodermMetalGene Expression Regulation DevelopmentalComputer Science Applications1707 Computer Vision and Pattern RecognitionExonsGeneral MedicineAnatomyMultigene familiemultigene familiesComputer Science ApplicationsCell biologymedicine.anatomical_structureMetalsMultigene FamilyParacentrotusEchinoderms; Embryonic development; Evolution; Gene expression; Metal; Metallothionein; Multigene families; Catalysis; Molecular Biology; Computer Science Applications1707 Computer Vision and Pattern Recognition; Spectroscopy; Physical and Theoretical Chemistry; Organic Chemistry; Inorganic ChemistryMesenchymeSettore BIO/11 - Biologia MolecolareIn situ hybridizationArticleCatalysisParacentrotus lividusInorganic Chemistry03 medical and health sciencesbiology.animalevolutionmedicineAnimalsGene familyProtein Interaction Domains and MotifsAmino Acid SequencePhysical and Theoretical ChemistryGeneMolecular BiologydevelopmentechinodermsOrganic Chemistrybiology.organism_classificationmetallothioneinAlternative Splicing030104 developmental biologyGene Expression RegulationEmbryonic developmentgene expression
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Molecular Docking approach on the Topoisomerase I inhibitors series included in the NCI anti-cancer agents mechanism database

2006

Topoisomerase I (Top1) is an essential enzyme participating to all those processes associated with separation of DNA strands. It manages superhelical tensions through the transient breakage of one strand of duplex DNA, followed by the unwinding of supercoiled DNA. Camptothecins, a class of alkaloids extracted from the wood of a Chinese tree, were found to be potent inhibitors of Topoisomerase I. The National Cancer Institute (NCI) Anti-cancer Agents Mechanism Database contains several camptothecins derivatives, classified as selective Top1 inhibitors. In this work we performed molecular docking studies on 24 camptothecin-like inhibitors present in this database (using Autodock 3.0.5). In or…

Models MolecularDatabases FactualProtein ConformationStereochemistryMolecular ConformationAntineoplastic AgentsTopoisomerase I inhibitorsTopoisomerase-I Inhibitorcomputer.software_genreCatalysisInorganic Chemistrychemistry.chemical_compoundEnzyme InhibitorsPhysical and Theoretical ChemistryAutodockchemistry.chemical_classificationBinding SitesDatabasebiologyTopoisomeraseOrganic ChemistryActive siteDNAAutoDockUnited StatesComputer Science ApplicationsEnzymeDNA Topoisomerases Type INational Institutes of Health (U.S.)Computational Theory and MathematicschemistryDocking (molecular)Molecular dockingbiology.proteinDNA supercoilCamptothecincomputerDNA
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DFT studies on the structural and vibrational properties of polyenes

2015

Detailed density functional theory (DFT) calculations on the structure and harmonic frequencies of model all-trans and all-cis polyenes were undertaken. For the first time, we report on the convergence of selected B3LYP/6-311++G** and BLYP/6-311++G** calculated structural parameters resulting from a systematic increase in polyene size (chains containing 2 to 14 C = C units). The limiting values of the structural parameters for very long chains were estimated using simple three-parameter empirical formulae. BLYP/6-311++G** calculated ν(C = C) and ν(C–C) frequencies for all-trans and all-cis polyenes containing up to 14 carbon–carbon double bonds were used to estimate these values for very lo…

Models MolecularDouble bondPolyenes02 engineering and technologyConjugated systemSpectrum Analysis RamanVibrationC-C bondAll-trans polyenesDFT01 natural sciencesMolecular physicsCatalysisInorganic ChemistryIR and Raman spectroscopychemistry.chemical_compoundComputational chemistry0103 physical sciencesWavenumberMoleculePhysical and Theoretical Chemistrychemistry.chemical_classificationOriginal Paper010304 chemical physicsChemistryOrganic ChemistryLimitingEthylenes021001 nanoscience & nanotechnologyPolyeneComputer Science ApplicationsC = C bondComputational Theory and MathematicsQuantum TheoryDensity functional theoryAll-cis polyenes0210 nano-technologyJournal of Molecular Modeling
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Molecular dynamics studies on HIV-1 protease: a comparison of the flap motions between wild type protease and the M46I/G51D double mutant

2007

The emergence of drug-resistant mutants of HIV-1 is a tragic effect associated with conventional long-treatment therapies against acquired immunodeficiency syndrome. These mutations frequently involve the aspartic protease encoded by the virus; knowledge of the molecular mechanisms underlying the conformational changes of HIV-1 protease mutants may be useful in developing more effective and longer lasting treatment regimes. The flap regions of the protease are the target of a particular type of mutations occurring far from the active site. These mutations modify the affinity for both substrate and ligands, thus conferring resistance. In this work, molecular dynamics simulations were perform…

Models MolecularGromacs 3.2Anti-HIV AgentsProtein Conformationmedicine.medical_treatmentflap motionMutantCatalysisVirusInorganic ChemistryProtein structureHIV ProteaseHIV-1 proteaseDrug Resistance ViralEnzyme StabilityHIV-1 proteasemedicineHumansComputer SimulationPhysical and Theoretical Chemistrychemistry.chemical_classificationProteasebiologyHIV-1 drug-resistant mutantOrganic ChemistryWild typeActive siteRecombinant ProteinsComputer Science ApplicationsCell biologyEnzymemolecular dynamics simulationAmino Acid SubstitutionComputational Theory and MathematicsBiochemistrychemistryMutationHIV-1biology.protein
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3-Chlorotyramine Acting as Ligand of the D2 Dopamine Receptor. Molecular Modeling, Synthesis and D2 Receptor Affinity.

2014

We synthesized and tested 3-chlorotyramine as a ligand of the D2 dopamine receptor. This compound displayed a similar affinity by this receptor to that previously reported for dopamine. In order to understand further the experimental results we performed a molecular modeling study of 3-chlorotyramine and structurally related compounds. By combining molecular dynamics simulations with semiempirical (PM6), ab initio and density functional theory calculations, a simple and generally applicable procedure to evaluate the binding energies of these ligands interacting with the D2 dopamine receptors is reported here. These results provided a clear picture of the binding interactions of these compou…

Models MolecularMolecular modelChemistryReceptors Dopamine D2Organic ChemistryBinding energyAtoms in moleculesAb initioTyramineComputer Science ApplicationsMolecular dynamicsDopamine D2 Receptor AntagonistsStructural BiologyDopamine receptorComputational chemistryDopamine receptor D2Drug DiscoveryHydrocarbons ChlorinatedMolecular MedicineHumansDensity functional theoryMolecular informatics
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Molecular Rearrangement of an Aza-Scorpiand Macrocycle Induced by pH: A Computational Study †

2016

Rearrangements and their control are a hot topic in supramolecular chemistry due to the possibilities that these phenomena open in the design of synthetic receptors and molecular machines. Macrocycle aza-scorpiands constitute an interesting system that can reorganize their spatial structure depending on pH variations or the presence of metal cations. In this study, the relative stabilities of these conformations were predicted computationally by semi-empirical and density functional theory approximations, and the reorganization from closed to open conformations was simulated by using the Monte Carlo multiple minimum method Financial support by the Spanish Ministerio de Economía y Competitiv…

Models MolecularMontecarlo Mètode deMonte Carlo method01 natural sciencessupramolecular chemistryMonte Carlo Multiple Minimumlcsh:ChemistryComputational chemistryaza-scorpiandsMolecular rearrangementpH controlled; supramolecular chemistry; synthetic receptors; aza-scorpiands; semi-empirical; Density Functional Theory; Monte Carlo Multiple Minimumlcsh:QH301-705.5semi-empiricalSpectroscopyDensity Functional TheoryDensity functionalsSpatial structureChemistryGeneral MedicineHydrogen-Ion ConcentrationMolecular machineComputer Science ApplicationsMonte Carlo methodpH controlledvisual_artsynthetic receptorsvisual_art.visual_art_mediumDensity functional theoryMonte Carlo MethodMacrocyclic CompoundsSupramolecular chemistry010402 general chemistryQuímica supramolecularCatalysisArticleInorganic ChemistryMetalQuantitative Biology::Subcellular ProcessesPhysical and Theoretical ChemistryMolecular BiologyAza CompoundsFuncional de densitat Teoria del010405 organic chemistryOrganic ChemistryComputational Biology0104 chemical scienceslcsh:Biology (General)lcsh:QD1-999Synthetic ReceptorsQuantum TheorySupramolecular chemistryInternational Journal of Molecular Sciences
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Docking and multivariate methods to explore HIV-1 drug-resistance: a comparative analysis

2007

In this paper we describe a comparative analysis between multivariate and docking methods in the study of the drug resistance to the reverse transcriptase and the protease inhibitors. In our early papers we developed a simple but efficient method to evaluate the features of compounds that are less likely to trigger resistance or are effective against mutant HIV strains, using the multivariate statistical procedures PCA and DA. In the attempt to create a more solid background for the prediction of susceptibility or resistance, we carried out a comparative analysis between our previous multivariate approach and molecular docking study. The intent of this paper is not only to find further supp…

Models MolecularMultivariate statisticsMultivariate analysisAnti-HIV AgentsCombined useHuman immunodeficiency virus (HIV)Computational biologyDrug resistanceBiologyLigandsBioinformaticsmedicine.disease_causeHIV ProteaseMolecular descriptorDrug Resistance ViralDrug DiscoverymedicineHumansDOCKINGPhysical and Theoretical ChemistryBinding SitesHIV Protease InhibitorsSettore CHIM/08 - Chimica FarmaceuticaHIV Reverse TranscriptaseComputer Science ApplicationsDRUG RESISTANCEDocking (molecular)Drug DesignMultivariate AnalysisMutationHIV-1Computer-Aided DesignReverse Transcriptase InhibitorsMultivariate statisticalJournal of Computer-Aided Molecular Design
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In-silico screening of new potential Bcl-2/Bcl-xl inhibitors as apoptosis modulators

2008

One of the major problems in the fight against cancer is drug-resistance, which, at a molecular level, can be acquired through mutations able to deactivate apoptosis. In particular, proteins in the Bcl-2 family are central regulators of programmed cell death, and members that inhibit apoptosis, such as Bcl-xl and Bcl-2, are overexpressed in many tumours. The development of new inhibitors of these proteins as potential anticancer therapeutics represents a new frontier. In this work, we carried out an in-silico screening of compounds from a free database of more than 2 million structures (ZINC database), which allowed us to identify 17 sulfonamide derivatives as new potential inhibitors; thes…

Models MolecularProgrammed cell deathDatabases FactualIn silicobcl-X ProteinAntineoplastic AgentsApoptosisBcl-xLDrug resistanceBiologyCatalysisInorganic ChemistryNeoplasmsmedicineAnimalsHumansPhysical and Theoretical ChemistryOrganic ChemistrySulfonamide (medicine)CancerApoptosis Bcl-2 Bcl-xl Inhibitors Molecular dockingmedicine.diseaseSettore CHIM/08 - Chimica FarmaceuticaMolecular medicineComputer Science ApplicationsCell biologyComputational Theory and MathematicsDrug Resistance NeoplasmApoptosisCancer researchbiology.proteinDrug Screening Assays Antitumormedicine.drugJournal of Molecular Modeling
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