Search results for "THERMODYNAMICS"

showing 10 items of 2774 documents

Nuclear receptors modulate the interaction of Sp1 and GC-rich DNA via ternary complex formation

2000

Binding sites for transcription factor Sp1have been implicated in the transcriptional regulation of several genes by hormones or vitamins, and here we show that a GC-rich element contributes to the retinoic acid response of the interleukin 1β promoter. To explain such observations, it has been proposed that nuclear receptors can interact with Sp1 bound to GC-rich DNA. However, evidence supporting this model has remained indirect. So far, nuclear receptors have not been detected in a complex with Sp1 and GC-rich DNA, and the expected ternary complexes in non-denaturing gels were not seen. In search for these missing links we found that nuclear receptors [retinoic acid receptor (RAR), thyroid…

Cell ExtractsTranscriptional ActivationReceptors Retinoic AcidSp1 Transcription FactorRecombinant Fusion ProteinsReceptors Cytoplasmic and NuclearTretinoinRetinoic acid receptor betaBiologyRetinoid X receptorLigandsResponse ElementsTransfectionModels BiologicalBiochemistryAntibodiesCell LineSubstrate SpecificityAnimalsPromoter Regions GeneticMolecular BiologyNuclear receptor co-repressor 1Nuclear receptor co-repressor 2Binding SitesReceptors Thyroid HormoneDNACell BiologyRetinoic acid receptor gammaRetinoid X receptor gammaGC Rich SequenceProtein Structure TertiaryNuclear receptor coactivator 1Retinoic acid receptorDrosophila melanogasterEcdysteroneRetinoid X ReceptorsOligodeoxyribonucleotidesBiochemistryReceptors CalcitriolThermodynamicsResearch ArticleInterleukin-1Protein BindingTranscription FactorsBiochemical Journal
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Quantitative characterization of tetraspanin 8 homointeractions in the plasma membrane

2021

The spatial distribution of proteins in cell membranes is crucial for signal transduction, cell communication and membrane trafficking. Members of the Tetraspanin family organize functional protein clusters within the plasma membrane into so-called Tetraspanin-enriched microdomains (TEMs). Direct interactions between Tetraspanins are believed to be important for this organization. However, studies thus far have utilized mainly co-immunoprecipitation methods that cannot distinguish between direct and indirect, through common partners, interactions. Here we study Tetraspanin 8 homointeractions in living cells via quantitative fluorescence microscopy. We demonstrate that Tetraspanin 8 exists i…

Cell signalingTetraspaninsLipoylationDimerTransfectionBiochemistryArticleProtein–protein interactionchemistry.chemical_compoundMembrane MicrodomainsTetraspaninFluorescence Resonance Energy TransferHumansMolecular BiologyChemistryCell BiologyDissociation constantHEK293 CellsMembraneMicroscopy FluorescenceMembrane proteinembryonic structuresBiophysicsThermodynamicsProtein MultimerizationSignal transductionSignal TransductionBiochemical Journal
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Intrinsic Acidity of Surface Sites in Calcium Silicate Hydrates and Its Implication to Their Electrokinetic Properties

2014

Calcium Silicate Hydrates (C–S–H) are the major hydration products of portland cement paste. The accurate description of acid–base reactions at the surface of C–S–H particles is essential for both understanding the ion sorption equilibrium in cement and prediction of mechanical properties of the hardened cement paste. Ab initio molecular dynamics simulations at the density functional level of theory were applied to calculate intrinsic acidity constants (pKa’s) of the relevant ≡SiOH and ≡CaOH2 groups on the C–S–H surfaces using a thermodynamic integration technique. Ion sorption equilibrium in C–S–H was modeled applying ab initio calculated pKa’s in titrating Grand Canonical Monte Carlo simu…

CementQuantitative Biology::BiomoleculesChemistryAb initioThermodynamicsThermodynamic integrationSorptionElectrolyteSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionElectrokinetic phenomenachemistry.chemical_compoundPortland cementGeneral EnergylawCalcium silicate550 Earth sciences & geologyPhysical chemistry[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Physical and Theoretical ChemistryPhysics::Chemical PhysicsComputingMilieux_MISCELLANEOUS
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Experimental investigation of calcium silicate hydrate (C-S-H) nucleation

1999

Due to the importance of calcium silicate hydrate (C-S-H) in cement chemistry, its nucleation mode and parameters influencing it were investigated. It has been observed that the C-S-H nucleation follows the general laws governing the nucleation. The degree of supersaturation has been found to be the main parameter controlling homogeneous nucleation rates. The lime concentration in solution, well known to be the most important parameter determining the kinetic, morphological and structural features of C-S-H, also controls the nucleation characteristics of heterogeneous nucleation, i.e. during hydration of cement. The correlation between heterogeneous nucleation of C-S-H and possible final me…

CementSupersaturationInorganic chemistryNucleationThermodynamicsengineering.materialCondensed Matter PhysicsKinetic energyInorganic Chemistrychemistry.chemical_compoundchemistryCalcium silicateMaterials ChemistryengineeringCalcium silicate hydrateHydrateLimeJournal of Crystal Growth
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Centrifuge tests on strip footings on sand with a weak layer

2017

Tests on small-scale physical models of a strip footing resting on a dense sand bed containing a thin horizontal weak soil layer were carried out at normal gravity (1 g ). The results, reported in a companion paper, point out that the weak layer plays an important role in the failure mechanism and the ultimate bearing capacity of the footing if it falls within the ground volume relevant to the behaviour of the sand–footing system. The same problem was also investigated by means of centrifuge tests on reduced-scale models at 25 g and 40 g . The results of these tests, reported and discussed in this paper, confirm that failure mechanisms are governed substantially by the presence of the weak…

CentrifugeGravity (chemistry)Physical modelgeotechnical engineering models (physical)shallow foundationsSettore ICAR/07 - Geotecnicageotechnical engineering0211 other engineering and technologiesgeotechnical engineering/models (physical)/shallow foundations02 engineering and technologyGeotechnical Engineering and Engineering GeologyCritical valueNO020303 mechanical engineering & transports0203 mechanical engineeringShallow foundationVolume (thermodynamics)Geotechnical engineeringBearing capacitymodels (physical)Layer (electronics)Geology021101 geological & geomatics engineeringshallow foundations
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Comparative computational analysis of different active site conformations and substrates in a chalcone isomerase catalyzed reaction.

2006

Chalcone isomerase catalyzes the transformation of chalcones to flavanones. We present a computational study of the rate-limiting chemical step, an intramolecular Michael addition of a 2'-oxyanion to the alpha,beta-double bound. By using quantum mechanical/molecular mechanical hybrid methods we traced the free-energy profiles associated with the reaction of two different substrates (chalcone and 6'-deoxychalcone) in two different conformations of the active site that are described in the different crystallographic structures available. We have obtained significant differences (about 4 kcal/mol) in the free-energy barriers calculated for the two active sites. According to our results, the ac…

Chalcone isomeraseAnionsModels MolecularChalconeStereochemistryProtein ConformationMolecular ConformationCatalysisCatalysischemistry.chemical_compoundAtomMaterials ChemistryComputer SimulationPhysical and Theoretical ChemistryIntramolecular LyasesBinding SitesbiologyActive siteSubstrate (chemistry)Hydrogen-Ion ConcentrationCarbonSurfaces Coatings and FilmsKineticschemistryModels ChemicalIntramolecular forcebiology.proteinMichael reactionQuantum TheoryThermodynamicsSoftwareThe journal of physical chemistry. B
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Nonlocal (Pair Site) Reactivity from Second-Order Static Density Response Function:  Gas- and Solution-Phase Reactivity of the Acetaldehyde Enolate a…

1999

A nonlocal (pair site) reactivity scheme is developed and tested. The theory is cast in terms of the first-order Fukui response function f(r,r‘), previously proposed by Fuentealba and Parr [J. Chem. Phys. 1991, 94, 5559]. A change of variables is introduced by using the softness s(r) and t(r) = [∂s(r)/∂N]υ(r) (the variation of softness with respect to the changes in the total number of electrons N at constant external potential υ(r)) that leads to a simple expression for the variation of the Fukui function at site k, namely = − for an electrophilic attack. The first term describes a local contribution, proportional to the variation of the electrostatic potential that can be induced, for exa…

Change of variables (PDE)Computational chemistryChemistryOrder (group theory)ThermodynamicsReactivity (chemistry)ElectronFunction (mathematics)Physical and Theoretical ChemistryConstant (mathematics)Fukui functionVariable (mathematics)The Journal of Physical Chemistry A
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Thermomechanical effects in the flow of a fluid in porous media

2002

This paper deals with analysis, by methods of extended thermodynamics, of the thermomechanical effects which arise in the flow of a weakly viscous fluid in a porous medium. Under the hypothesis that the fluid fills all the interstices among the powder and that the size of the powder grains and of the interstices is much lower than a suitable characteristic length, linearized field equations are written, which include, in a natural way, terms which take into account the Dufour, Soret, and virtual mass effects. As a limiting case when the evolution time of the heat flux goes to infinite and no entropy flux is carried, the flow of liquid helium II in a porous medium is obtained.

Characteristic lengthThermodynamicsViscous liquidComputer Science ApplicationsPhysics::Fluid DynamicsHeat fluxModeling and SimulationMass transferModelling and SimulationHeat transferFluid dynamicsBoundary value problemPorous mediumMathematicsMathematical and Computer Modelling
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Diffusion of Oxygen through Cork Stopper: Is It a Knudsen or a Fickian Mechanism?

2014

International audience; The aim of this work is to identify which law governs oxygen transfer through cork: Knudsen or Fickian mechanism. This is important to better understand wine oxidation during post-bottling aging. Oxygen transfer through cork wafers is measured at 298 K using a manometric permeation technique. Depending on the mechanism, we can extract the transport coefficients. Increasing the initial pressure of oxygen from 50 to 800 hPa leads to a change in the values of the transport coefficients. This implies that oxygen transport through cork does not obey the Knudsen law. From these results, we conclude that the limiting step of oxygen transport through cork occurs in the cell …

Chemical PhenomenaDiffusionchemistry.chemical_elementThermodynamicsWineCorkengineering.materialOxygenPermeabilityQuercusactivation volume[CHIM]Chemical SciencesdiffusionFood PackagingOxygen transportGeneral ChemistryPermeationFick's laws of diffusionOxygenchemistryVolume (thermodynamics)oxygen transportengineeringThermodynamicspermeationGasesKnudsen numbercork stopperGeneral Agricultural and Biological SciencesOxidation-Reduction
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Chemical and catalytical properties of thermal polymers of amino acids (proteinoids)

1974

The significance of thermal polyamino acids (proteinoids) as abiotic predecessors of proteins is reviewed on the basis of new experimental results. Most proteinoids yield only 50% to 80% amino acid upon acid hydrolysis. They contain 40% to 60% less peptide links than typical proteins, whereas their average nitrogen content is like that of proteins. The arrangement of amino acid residues is nonrandom. The degree of nonrandomness is difficult to determine because unusual crosslinks disturb most of the sequencing methods typically applied in protein chemistry. The products obtained in a polymerization experiment are heterogeneous. They can be separated into a limited number of related fraction…

Chemical PhenomenaMacromolecular SubstancesPolymersOrigin of LifePeptideCatalysisChromatography DEAE-CelluloseProteinoidOrganic chemistryAmino Acid SequenceAmino AcidsMolecular BiologyEcology Evolution Behavior and SystematicsGeneral Environmental Sciencechemistry.chemical_classificationMolecular massHydrolysisProteinsGeneral MedicinePolymerHydrogen-Ion ConcentrationElectrophoresis DiscBiological EvolutionAgricultural and Biological Sciences (miscellaneous)Amino acidMolecular WeightChemistrySolubilitychemistryPolymerizationSpace and Planetary ScienceYield (chemistry)ThermodynamicsGeneral Earth and Planetary SciencesAcid hydrolysisOrigins of Life
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