Search results for "Hydrophobic effect"

showing 10 items of 74 documents

Enthalpy/entropy compensation effects from cavity desolvation underpin broad ligand binding selectivity for rat odorant binding protein 3

2014

Evolution has produced proteins with exquisite ligand binding specificity, and manipulating this effect has been the basis for much of modern rational drug design. However, there are general classes of proteins with broader ligand selectivity linked to function, the origin of which is poorly understood. The odorant binding proteins (OBPs) sequester volatile molecules for transportation to the olfactory receptors. Rat OBP3, which we characterize by X-ray crystallography and NMR, binds a homologous series of aliphatic gamma-lactones within its aromatic-rich hydrophobic pocket with remarkably little variation in affinity but extensive enthalpy/entropy compensation effects. We show that the bin…

Models Molecular[SDV.BIO]Life Sciences [q-bio]/BiotechnologyOdorant bindingolfactory receptor[ SDV.AEN ] Life Sciences [q-bio]/Food and NutritionEnthalpywaterDrug designCrystallography X-RayLigandsReceptors Odorantentropy compensationBiochemistryHydrophobic effectLactonesdifferent chemical classessiteAnimalsMoleculeNuclear Magnetic Resonance Biomolecularisotopically enriched proteinsbiologyChemistrycarbonic-anhydrase[ SDV.BIO ] Life Sciences [q-bio]/BiotechnologyLigand (biochemistry)RatsCrystallographyEnthalpy–entropy compensationSolventsOdorant-binding proteinbiology.proteinBiophysicsThermodynamicsidentificationrecognitionsolvent reorganization[SDV.AEN]Life Sciences [q-bio]/Food and NutritionProtein Binding
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Collective properties of hydration: long range and specificity of hydrophobic interactions

1997

We report results of molecular dynamics (MD) simulations of composite model solutes in explicit molecular water solvent, eliciting novel aspects of the recently demonstrated, strong many-body character of hydration. Our solutes consist of identical apolar (hydrophobic) elements in fixed configurations. Results show that the many-body character of PMF is sufficiently strong to cause 1) a remarkable extension of the range of hydrophobic interactions between pairs of solute elements, up to distances large enough to rule out pairwise interactions of any type, and 2) a SIF that drives one of the hydrophobic solute elements toward the solvent rather than away from it. These findings complement re…

Models Molecularchemistry.chemical_classificationRange (particle radiation)BiomoleculeBiophysicsWaterEnergy landscapeSolutionsFolding (chemistry)Hydrophobic effectMolecular dynamicsCharacter (mathematics)Models ChemicalchemistryChemical physicsComputational chemistrySolventsProtein recognitionThermodynamicsComputer SimulationResearch ArticleBiophysical Journal
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Phosphatidylcholine covalently linked to a methacrylate-based monolith as a biomimetic stationary phase for capillary liquid chromatography

2015

Abstract In this study a strategy to immobilize phospholipids onto a polymer-based stationary phase is described. Methacrylate-based monoliths in capillary format (150 × 0.1 mm) were modified by soybean phosphatidylcholine through 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide coupling to obtain stationary phases suitable to mimic cell surface membranes. The covalent coupling reaction involves the phosphate group in phospholipids; therefore, the described methodology is suitable for all types of phospholipids. Immobilization of soy bean phosphatidylcholine on the monolith was confirmed by attenuated total reflectance Fourier transform infrared spectroscopy and gas chromatography-mass spectro…

Monolithic HPLC columnPolymersPhospholipid010402 general chemistryMethacrylate01 natural sciencesBiochemistryChemistry Techniques AnalyticalAnalytical ChemistryHydrophobic effectchemistry.chemical_compoundBiomimeticsEthyldimethylaminopropyl CarbodiimidePhosphatidylcholineMonolithFourier transform infrared spectroscopyPhospholipidsgeographygeography.geographical_feature_categoryChromatography010401 analytical chemistryOrganic ChemistryWaterGeneral Medicine0104 chemical sciencesMembranechemistryPhosphatidylcholinesMethacrylatesHydrophobic and Hydrophilic InteractionsChromatography LiquidJournal of Chromatography A
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Micellar versus hydro-organic mobile phases for retention-hydrophobicity relationship studies with ionizable diuretics and an anionic surfactant

2004

Abstract Logarithm of retention factors (log  k ) of a group of 14 ionizable diuretics were correlated with the molecular (log  P o/w ) and apparent (log  P app ) octanol–water partition coefficients. The compounds were chromatographed using aqueous–organic (reversed-phase liquid chromatography, RPLC) and micellar–organic mobile phases (micellar liquid chromatography, MLC) with the anionic surfactant sodium dodecyl sulfate (SDS), in the pH range 3–7, and a conventional octadecylsilane column. Acetonitrile was used as the organic modifier in both modes. The quality of the correlations obtained for log  P app at varying ionization degree confirms that this correction is required in the aqueou…

OctanolsChromatographyStatic ElectricityOrganic ChemistryAnalytical chemistryWaterGeneral MedicineReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryPartition coefficientHydrophobic effectSurface-Active Agentschemistry.chemical_compoundchemistryPulmonary surfactantMicellar liquid chromatographySpectrophotometry UltravioletSodium dodecyl sulfateDiureticsAcetonitrileChromatography High Pressure LiquidMicellesJournal of Chromatography A
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Effects of electric charges on hydrophobic forces. II.

2000

We study by molecular-dynamics simulations the effect of electric charges of either sign on hydrophobic interactions and on the dynamics of hydration water, using explicit water and very simplified solutes. Results show that the presence of a charged solute can disrupt the "hydrophobic contact bond" between two apolar solutes nearby, by forcing them towards a different configuration. As a consequence of different structural changes of the solvent caused by charges of opposite sign, the effect is markedly charge-sign-dependent. Analogous weaker effects appear to be induced by the presence of one additional apolar element. The dynamics of hydration water around each solute is also seen to be …

PhysicsHydrophobic effectMolecular dynamicsChemical physicsPhysical chemistryCharge (physics)Electric chargePhysical Review E
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Influence of End Groups on the Stimulus-Responsive Behavior of Poly[oligo(ethylene glycol) methacrylate] in Water

2010

The influence of the chemical structure of both end groups onto the lower critical solution temperature (LCST) of poly[oligo(ethylene glycol) monomethyl ether methacrylate] (POEGMA) in water was systematically investigated. POEGMA of Mn = 3550 g/mol and Mw/Mn = 1.14 prepared by reversible addition-fragmentation chain transfer (RAFT) polymerization was equipped with two different functional end groups in a one-step postpolymerization reaction combining activated esters, functional amines, and functional methane thiosulfonates. As end groups, n-propyl, n-hexadecyl, di(n-octadecyl), poly(ethylene glycol)-550 (PEG), 1H,1H-perfluorononyl, azobenzene, and trimethylethylammonium groups were system…

Polymers and PlasticsChemistryOrganic ChemistryChain transferLower critical solution temperatureMicelleInorganic ChemistryHydrophobic effectEnd-groupchemistry.chemical_compoundPolymerizationAzobenzenePolymer chemistryMaterials ChemistryEthylene glycolMacromolecules
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Kinetic evidence for the solubilization of pyridine-2-azo-p-dimethylaniline in alkanediyl-α,ω-bis(dimethylcetylammonium nitrate) surfactants. Role of…

2004

The incorporation of the bidentate ligand pyridine-2-azo-p-dimethylaniline (PADA) into micellar aggregates of the dimeric cationic surfactants propanediyl-, hexanediyl- and dodecanediyl-alpha,omega-bis(dimethylcetylammonium nitrate) (16-3-16,2NO(3)(-), 16-6-16,2NO(3)(-) and 16-12-16,2NO(3)(-), respectively) has been studied at 25 degreesC by examining the kinetics of the complexation reaction of the Ni(II) ion with this ligand. For comparison, cetyltrimethylammonium nitrate ( CTAN), which can be considered as the "monomeric'' surfactant of 16-3-16,2NO(3)(-), has also been used. The kinetic data have shown that, for 16-3-16,2NO(3)(-) and CTAN, at a surfactant concentration below the critical…

Reaction mechanismInorganic chemistryMicelleCATIONIC GEMINI SURFACTANTSCatalysisHydrophobic effectReaction rate constantPulmonary surfactantDIMERIC SURFACTANTSPolymer chemistryMaterials ChemistryWATERELECTRON TRANSFERANGLE NEUTRON SCATTERINGInterfaces (materials) Optical waveguides metal ionsAqueous solutionAGGREGATION PROPERTIESChemistryAQUEOUS SOLUTIONCationic polymerizationGeneral ChemistryANIONIC MICELLESSUBSTITUTED FERROCENESCritical micelle concentrationBROMIDE SURFACTANTSANGLE NEUTRON SCATTERING; CATIONIC GEMINI SURFACTANTS; AQUEOUS SOLUTION; BROMIDE SURFACTANTS; DIMERIC SURFACTANTS; SUBSTITUTED FERROCENES; AGGREGATION PROPERTIES; ELECTRON TRANSFER; ANIONIC MICELLES; WATERNew J. Chem.
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High-Generation Amphiphilic Janus-Dendrimers as Stabilizing Agents for Drug Suspensions

2018

Pharmaceutical nanosuspensions are formed when drug crystals are suspended in aqueous media in the presence of stabilizers. This technology offers a convenient way to enhance the dissolution of poorly water-soluble drug compounds. The stabilizers exert their action through electrostatic or steric interactions, however, the molecular requirements of stabilizing agents have not been studied extensively. Here, four structurally related amphiphilic Janus-dendrimers were synthesized and screened to determine the roles of different macromolecular domains on the stabilization of drug crystals. Physical interaction and nanomilling experiments have substantiated that Janus-dendrimers with fourth gen…

Recrystallization (geology)huumeetPolymers and Plastics116 Chemical sciences02 engineering and technology01 natural sciencesdrugsContact angleMaterials ChemistryHUMAN LECTINSSurface plasmon resonanceta116chemistry.chemical_classificationChemistryBIOLOGICAL-MEMBRANES021001 nanoscience & nanotechnologyPROGRAMMABLE GLYCAN LIGANDSINDOMETHACIN317 PharmacyCLICK CHEMISTRYfarmaseuttinen kemia0210 nano-technologyHydrophobic and Hydrophilic InteractionsDendrimersSURFACEBioengineeringPoloxamer010402 general chemistryRSPOORLY SOLUBLE DRUGBiomaterialsHydrophobic effectSurface-Active AgentsSuspensionslääkeyhdisteetDendrimerAmphiphileGLYCODENDRIMERSOMESta216ta215AlkylMODULAR SYNTHESISWaterPoloxamerCombinatorial chemistry0104 chemical scienceslääkkeet1182 Biochemistry cell and molecular biologypharmaceutical nanosuspensionsCOMPLEX ARCHITECTURESBiomacromolecules
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Retention effect of human saliva on aroma release and respective contribution of salivary mucin and alpha-amylase

2014

International audience; As great differences were observed in the amount of alpha-amylase in human saliva, there is a need to better understand the effect of this protein alone or in mixture with mucin on aroma compound partitioning. We report. the respective role of mucin and alpha-amylase on the air/liquid partition coefficients of two series of 5 methylketones and 5 ethyl-esters. We confirm that mucin affects the release of aroma compounds and, for the first time, we demonstrate the ability of alpha-amylase to decrease the release of aroma compounds. For both proteins, we report the involvement of hydrophobic effects. Interestingly, no cumulative effect was observed when both proteins we…

Saliva030309 nutrition & dieteticsEsteraseHydrophobic effect03 medical and health scienceschemistry.chemical_compound0404 agricultural biotechnologyfluids and secretionsstomatognathic systemmucin[SDV.IDA]Life Sciences [q-bio]/Food engineeringAroma compoundAmylaseAroma0303 health sciencessalivaair/liquid partition coefficientbiologyMucinalpha-amylase04 agricultural and veterinary sciencesbiology.organism_classification040401 food sciencePartition coefficientchemistryBiochemistryaromabiology.protein[SDV.AEN]Life Sciences [q-bio]/Food and Nutritionhydrophobic effectFood Science
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Effect of T-R conformational change on sickle-cell hemoglobin interactions and aggregation

2004

We compare the role of a conformational switch and that of a point mutation in the thermodynamic stability of a protein solution and in the consequent propensity toward aggregation. We study sickle-cell hemoglobin (HbS), the beta6 Glu-Val point mutant of adult human hemoglobin (HbA), in its R (CO-liganded) conformation, and compare its aggregation properties to those of both HbS and HbA in their T (unliganded) conformation. Static and dynamic light scattering measurements performed for various hemoglobin concentrations showed critical divergences with mean field exponents as temperature was increased. This allowed determining spinodal data points T(S)(c) by extrapolation. These points were …

SpinodalConformational changeLightProtein ConformationEntropyHemoglobin SickleEnthalpyMolecular ConformationNucleationThermodynamicsProtein aggregationBiochemistryHydrophobic effectDynamic light scatteringStructural BiologySpectroscopy Fourier Transform InfraredHumansPoint MutationScattering RadiationMolecular BiologyCell AggregationCarbon MonoxideChemistryTemperatureProteinsHydrogen-Ion ConcentrationCrystallographyModels ChemicalSpectrophotometryThermodynamicsProtein BindingEntropy (order and disorder)Proteins: Structure, Function, and Bioinformatics
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