Search results for "Surfaces"

showing 10 items of 2837 documents

Elucidation of Carbohydrate Molecular Interaction Mechanism of Recombinant and Native ArtinM

2013

[EN] The quartz crystal microbalance (QCM) technique has been applied for monitoring the biorecognition of ArtinM lectins at low horseradish peroxidase glycoprotein (HRP) concentrations, using a simple kinetic model based on Langmuir isotherm in previous work.(18) The latter approach was consistent with the data at dilute conditions but it fails to explain the small differences existing in the jArtinM and rArtinM due to ligand binding concentration limit. Here we extend this analysis to differentiate sugar-binding event of recombinant (rArtinM) and native (jArtinM) ArtinM lectins beyond dilute conditions. Equivalently, functionalized quartz crystal microbalance with dissipation monitoring (…

Models MolecularPROTEIN ADSORPTIONSURFACEKM+Horseradish peroxidaselaw.inventionsymbols.namesakelawQUARTZ-CRYSTAL MICROBALANCEBINDINGQUIMICA ANALITICAMaterials ChemistryPhysical and Theoretical ChemistrySPECIFICITYGlycoproteinsBinding SitesChromatographybiologyChemistryLectinLangmuir adsorption modelQuartz crystal microbalanceQuartz Crystal Microbalance TechniquesLECTINRecombinant ProteinsSurfaces Coatings and FilmsMannose-Binding LectinsSolvation shellHYDRATION-SHELLQuartz Crystal Microbalance TechniquesBiophysicsbiology.proteinRecombinant DNAsymbolsPlant LectinsBIOMOLECULAR ADSORPTIONARTOCARPINProtein adsorption
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Interfacial behavior of recombinant forms of human pulmonary surfactant protein SP-C.

2012

The behavior at air-liquid interfaces of two recombinant versions of human surfactant protein SP-C has been characterized in comparison with that of native palmitoylated SP-C purified from porcine lungs. Both native and recombinant proteins promoted interfacial adsorption of dipalmitoylphosphatidylcholine bilayers to a limited extent, but catalyzed very rapid formation of films from different lipid mixtures containing both zwitterionic and anionic phospholipids. Once at the interface, the recombinant variants exhibited compression-driven structural transitions, consistent with changes in the orientation of the deacylated N-terminal segment, which were not observed in the native protein. Com…

Models MolecularProtein ConformationSurface PropertiesMolecular Sequence DataCatalysislaw.inventionchemistry.chemical_compoundAdsorptionPulmonary surfactantlawMoleElectrochemistryMoleculeNative proteinAnimalsHumansGeneral Materials ScienceAmino Acid SequenceSpectroscopyPhospholipidsSurfaces and InterfacesCondensed Matter PhysicsPulmonary Surfactant-Associated Protein CPeptide FragmentsRecombinant ProteinschemistryBiochemistryDipalmitoylphosphatidylcholineRecombinant DNABiophysicsLangmuir : the ACS journal of surfaces and colloids
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Theoretical Study of the Catalytic Mechanism of DNA-(N4-Cytosine)-Methyltransferase from the Bacterium Proteus vulgaris

2010

In this paper the reaction mechanism for methylation of cytosine at the exocyclic N4 position catalyzed by M.PvuII has been explored by means of hybrid quantum mechanics/molecular mechanics (QM/MM) methods. A reaction model was prepared by placing a single cytosine base in the active site of the enzyme. In this model the exocyclic amino group of the base establishes hydrogen bond interactions with the hydroxyl oxygen atom of Ser53 and the carbonyl oxygen atom of Pro54. The reaction mechanism involves a direct methyl transfer from AdoMet to the N4 atom and a proton transfer from this atom to Ser53, which in turn transfers a proton to Asp96. Different timings for the proton transfers and meth…

Models MolecularReaction mechanismProtonbiologyHydrogen bondStereochemistrySite-Specific DNA-Methyltransferase (Cytosine-N4-Specific)Active siteMethylationDNA MethylationPhotochemistryProtein Structure TertiarySurfaces Coatings and FilmsCatalysischemistry.chemical_compoundchemistryBiocatalysisMaterials Chemistrybiology.proteinProteus vulgarisQuantum TheoryPhysical and Theoretical ChemistryCytosineDNAThe Journal of Physical Chemistry B
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Magneto-optical nanomaterials: a SPIO–phthalocyanine scaffold built step-by-step towards bimodal imaging

2013

A SPIO-phthalocyanine nanohybrid is developed as a bimodal contrast agent for Optical and Magnetic Resonance Imaging. The organic coating was covalently attached onto SPIO in a step-by-step approach. Each coated-SPIO was thoroughly characterized. The hydrodynamic size of the SPIO-Pc is ca. 60 nm with a coverage of ca. 690 Pc/SPIO.

Models MolecularScaffoldIndolesMaterials scienceContrast MediaNanoparticleNanotechnology02 engineering and technologyIsoindolesengineering.material010402 general chemistry01 natural sciencesCatalysisNanomaterialsMagneto opticalchemistry.chemical_compoundCoatingMaterials Chemistry[CHIM]Chemical SciencesComputingMilieux_MISCELLANEOUSMetals and AlloysGeneral Chemistry021001 nanoscience & nanotechnologyMagnetic Resonance ImagingFerrosoferric Oxide0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryCeramics and CompositesPhthalocyanineengineeringNanoparticles0210 nano-technologyChemical Communications
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Comparative Studies on IR, Raman, and Surface Enhanced Raman Scattering Spectroscopy of Dipeptides Containing ΔAla and ΔPhe

2012

Three dipeptides containing dehydroresidues (\DeltaAla, \Delta (Z)Phe, and \Delta (E)Phe) were examined by IR, Raman, and surface-enhanced Raman techniques for the first time. The effect of the size and isomer type of the β -substituent in the dehydroresidue on the conformational structure of the peptide was evaluated by using the analysis of IR and Raman bands. Additionally, SERS spectroscopy provided insight into the adsorption mechanism of these species on the metal surface. SERS spectra were recorded at alkaline pH on the silver sol using visible light excitation. The dehydroresidues studied here strongly influenced the SERS profile of the peptides. The most pronounced SERS signal for a…

Models MolecularSpectrophotometry InfraredSurface PropertiesPhenylalanineAnalytical chemistryMolecular ConformationSpectrum Analysis RamanVibrationMetalchemistry.chemical_compoundsymbols.namesakeAdsorptionDeprotonationSpectrophotometryMaterials ChemistrymedicineCarboxylatePhysical and Theoretical ChemistrySpectroscopyAlaninemedicine.diagnostic_testDipeptidesSurfaces Coatings and FilmsCrystallographychemistryMetalsvisual_artvisual_art.visual_art_mediumsymbolsRaman spectroscopyVisible spectrumJournal of Physical Chemistry B
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Calorimetric Behavior of Phosphatidylcholine/Phosphatidylethanolamine Bilayers is Compatible with the Superlattice Model

2012

Differential scanning calorimetry was used to study the phase behavior of binary lipid bilayers consisting of phosphatidylcholine (PC) and phosphatidylethanolamine (PE) of varying acyl chain length. A two-state transition model was used to resolve the individual transition components, and the two-state transition enthalpy, the relative enthalpy, and the transition temperature of each component were plotted as a function of composition. Intriguingly, abrupt changes in these thermodynamic parameters were observed at or close to many "critical" X(PE) values predicted by the superlattice model proposing that phospholipids with different headgroups tend to adopt regular rather than random latera…

Models MolecularSuperlatticeLipid BilayersEnthalpyAnalytical chemistryThermodynamics02 engineering and technologyCalorimetryArticle03 medical and health scienceschemistry.chemical_compoundDifferential scanning calorimetryPhase (matter)PhosphatidylcholineMaterials ChemistryTransition TemperaturePhysical and Theoretical ChemistryLipid bilayer030304 developmental biologyPhysics::Biological Physics0303 health sciencesCalorimetry Differential ScanningChemistryPhosphatidylethanolaminesTransition temperature021001 nanoscience & nanotechnologySurfaces Coatings and FilmsPhosphatidylcholinesThermodynamics0210 nano-technologyThe Journal of Physical Chemistry B
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Modeling of the role of conformational dynamics in kinetics of the antigen-antibody interaction in heterogeneous phase.

2012

[EN] A novel approach that may potentially be used to study biomolecular interactions including the simultaneous determination of structural and kinetic binding parameters is described in this Article for the first time. It allows a rigid distinction between the possible reaction mechanisms of biomolecular recognition, induced fit and conformational selection. The relative importance of the two pathways is determined not by comparing rate constants but the structural aspects of the interaction instead. So the exact location of antigen molecules with respect to the capture antibody is depicted experimentally, avoiding the use of X-ray crystallography. The proposed pattern is applied to study…

Models MolecularTime FactorsSimultaneous determinationsProtein ConformationRate constantsBinding processAntigen-Antibody ComplexImmunoglobulin GFragment antigen-bindingConformational dynamicsMiceStructural aspectsBiomolecular recognitionMaterials ChemistrySteric hindrancesBovine serum albuminReaction mechanismbiologyChemistryIn-situSerum Albumin BovineLigand (biochemistry)Reaction schemesSurfaces Coatings and FilmsConformationsAntigen-antibody interactionBovine serum albuminsBiomolecular interactionsMolecular recognitionBSA moleculesAlgorithmsProtein BindingStereochemistryKinetic bindingReaction intermediateAntigen bindingAntibodiesMolecular recognitionAntigenQUIMICA ANALITICAAnimalsComputer SimulationPhysical and Theoretical ChemistryAntigensHeterogeneous phaseInduced fitX ray crystallographyMoleculesSensing surfaceKineticsSilicon chipInterferometryConformational selectionImmunoglobulin Gbiology.proteinBiophysicsCattleAntigen-antibody interactionThe journal of physical chemistry. B
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Theoretical insight into the intrinsic ultrafast formation of cyclobutane pyrimidine dimers in UV-irradiated DNA: thymine versus cytosine.

2008

The higher formation yields measured in the ultrafast photoinduced formation of cyclobutane thymine dimers (T T) with respect to those of cytosine (C C) are explained, on the basis of ab initio CASPT2 results, by the existence in thymine of more reactive orientations and a less efficient photoreversibility, whereas in cytosine the funnel toward the photolesion becomes competitive with that mediating the internal conversion of the excited-cytosine monomer.

Models MolecularTime FactorsUltraviolet RaysAb initioPyrimidine dimerDNAInternal conversion (chemistry)PhotochemistrySurfaces Coatings and FilmsThymineCyclobutanechemistry.chemical_compoundCytosineMonomerchemistryPyrimidine DimersMaterials ChemistryNucleic Acid ConformationPhysical and Theoretical ChemistryCytosineDNAThymineDNA DamageThe journal of physical chemistry. B
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Delivery modulation in silica mesoporous supports via alkyl chain pore outlet decoration

2012

This article focuses on the study of the release rate in a family of modified silica mesoporous supports. A collection of solids containing ethyl, butyl, hexyl, octyl, decyl, octadecyl, docosyl, and triacontyl groups anchored on the pore outlets of mesoporous MCM-41 has been prepared and characterized. Controlled release from pore voids has been studied through the delivery of the dye complex tris(2,2¿-bipyridyl)ruthenium(II). Delivery rates were found to be dependent on the alkyl chain length anchored on the pore outlets of the mesoporous scaffolding. Moreover, release rates follow a Higuchi diffusion model, and Higuchi constants for the different hybrid solids have been calculated. A decr…

Models MolecularTrisINGENIERIA DE LA CONSTRUCCIONSurface Propertieschemistry.chemical_elementMolecular Dynamics SimulationMolecular dynamicschemistry.chemical_compoundQUIMICA ORGANICAOrganometallic CompoundsElectrochemistryOrganic chemistryGeneral Materials ScienceParticle SizePorositySpectroscopyAlkylchemistry.chemical_classificationQUIMICA INORGANICASurfaces and InterfacesSilicon DioxideCondensed Matter PhysicsControlled releaseRutheniumChemical engineeringchemistryParticle sizeMesoporous materialPorosity
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Theoretical Study of the Hydroxyl Radical Addition to Uracil and Photochemistry of the Formed U6OH• Adduct

2014

Hydroxyl radical ((•)OH) is produced in biological systems by external or endogenous agents. It can damage DNA/RNA by attacking pyrimidine nucleobases through the addition to the C5═C6 double bond. The adduct resulting from the attachment at the C5 position prevails in the experimental measurements, although the reasons for this preference remain unclear. The first aim of this work is therefore to shed light on the comprehension of this important process. Thus, the thermal (•)OH addition to the C5═C6 double bond of uracil has been studied theoretically by using DFT, MP2, and the multiconfigurational CASPT2//CASSCF methodologies. The in-vacuo results obtained with the latter protocol plus th…

Models Molecularchemistry.chemical_classificationPyrimidineDouble bondHydroxyl RadicalPhotochemistryUracilPhotochemistrySurfaces Coatings and FilmsAdductNucleobaseDNA Adductschemistry.chemical_compoundchemistryMaterials ChemistryQuantum TheoryHydroxyl radicalPhysical and Theoretical ChemistrySolvent effectsUracilVisible spectrumThe Journal of Physical Chemistry B
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