Search results for "hydrophobic"

showing 10 items of 332 documents

Transmembrane but not soluble helices fold inside the ribosome tunnel

2018

Integral membrane proteins are assembled into the ER membrane via a continuous ribosome-translocon channel. The hydrophobicity and thickness of the core of the membrane bilayer leads to the expectation that transmembrane (TM) segments minimize the cost of harbouring polar polypeptide backbones by adopting a regular pattern of hydrogen bonds to form α-helices before integration. Co-translational folding of nascent chains into an α-helical conformation in the ribosomal tunnel has been demonstrated previously, but the features governing this folding are not well understood. In particular, little is known about what features influence the propensity to acquire α-helical structure in the ribosom…

Protein FoldingSequence Homology Amino AcidScienceQProteïnes de membranaMembrane ProteinsMolecular Dynamics SimulationEndoplasmic ReticulumArticleProtein Structure SecondaryAnimalslcsh:QAmino Acid Sequencelcsh:ScienceHydrophobic and Hydrophilic InteractionsSignal Recognition ParticleRibosomes
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Metamagnetism in hydrophobically induced carboxylate (phenylmalonate)-bridged copper(II) layers

2006

Self-assembly of copper(II) ions, phenylmalonate and pyrimidine yields the layered compound [Cu(pym)(Phmal)]n ( 1) where intralayer ferro- and interlayer antiferromagnetic interactions occur with three-dimensional antiferromagnetic ordering at Tc = 2.15 K Lloret Pastor, Francisco, Francisco.Lloret@uv.es ; Julve Olcina, Miguel, Miguel.Julve@uv.es

PyrimidineUNESCO::QUÍMICAInorganic chemistrychemistry.chemical_element:QUÍMICA [UNESCO]CatalysisIonMetamagnetism ; Hydrophobically ; Copper ; Three-dimensional antiferromagneticchemistry.chemical_compoundThree-dimensional antiferromagneticMaterials ChemistryAntiferromagnetismCarboxylateMetamagnetismChemistryUNESCO::QUÍMICA::Química analíticaMetals and AlloysGeneral ChemistryHydrophobicallyCopperSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMetamagnetismCrystallographyCeramics and Composites:QUÍMICA::Química analítica [UNESCO]Copper
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Solvent-induced free energy landscape and solute-solvent dynamic coupling in a multielement solute

1999

AbstractMolecular dynamics simulations using a simple multielement model solute with internal degrees of freedom and accounting for solvent-induced interactions to all orders in explicit water are reported. The potential energy landscape of the solute is flat in vacuo. However, the sole untruncated solvent-induced interactions between apolar (hydrophobic) and charged elements generate a rich landscape of potential of mean force exhibiting typical features of protein landscapes. Despite the simplicity of our solute, the depth of minima in this landscape is not far in size from free energies that stabilize protein conformations. Dynamical coupling between configurational switching of the syst…

Quantitative Biology::BiomoleculesProtein ConformationChemistryBiophysicsDegrees of freedom (physics and chemistry)ProteinsEnergy landscapeMolecular Dynamics SimulationSolventMolecular dynamicsCoupling (computer programming)Chemical physicsComputational chemistrySolventsThermodynamicsProtein foldingPotential of mean forceHydrophobic and Hydrophilic InteractionsOrder of magnitudeResearch Article
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Determination of the hydrophobicity of organic compounds measured as logPo/w through a new chromatographic method

2009

A new chromatographic method to determine the octanol-water partition coefficient (logP(o/w)) of organic substances is proposed in this paper. This method is based on a previously reported model that relates the retention factor in reversed-phase liquid chromatography with solute (p), mobile phase (P(m)(N)) and stationary phase (P(s)(N)) polarity parameters: logk=(logk)(0)+p(P(m)(N)-P(s)(N)). P(m)(N) values are calculated through expressions that depend only on the organic solvent fraction in the mobile phase. (logk)(0) and P(s)(N) parameters are characteristic of the chromatographic system and are determined from the retention of a selected set of 12 compounds. Then, the p value of a solut…

Quantitative structure–activity relationshipChromatographyChemistryChemical structureOrganic ChemistryAnalytical chemistryQuantitative Structure-Activity RelationshipGeneral MedicineReversed-phase chromatographyHydrogen-Ion ConcentrationBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryPartition coefficientchemistry.chemical_compoundPhase (matter)LipophilicityOrganic ChemicalsAcetonitrileHydrophobic and Hydrophilic InteractionsChromatography LiquidJournal of Chromatography A
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Event-based criteria in GT-STAF information indices: theory, exploratory diversity analysis and QSPR applications

2012

Versatile event-based approaches for the definition of novel information theory-based indices (IFIs) are presented. An event in this context is the criterion followed in the "discovery" of molecular substructures, which in turn serve as basis for the construction of the generalized incidence and relations frequency matrices, Q and F, respectively. From the resultant F, Shannon's, mutual, conditional and joint entropy-based IFIs are computed. In previous reports, an event named connected subgraphs was presented. The present study is an extension of this notion, in which we introduce other events, namely: terminal paths, vertex path incidence, quantum subgraphs, walks of length k, Sach's subg…

Quantitative structure–activity relationshipEntropyChemistry OrganicInformation TheoryQuantitative Structure-Activity RelationshipBioengineeringInformation theoryJoint entropyMolecular descriptorDrug DiscoveryComputer GraphicsCluster AnalysisEntropy (information theory)QuantumMathematicsDiscrete mathematicsMolecular StructureLinear modelComputational BiologyGeneral MedicineEthylenesModels TheoreticalLinear ModelsMolecular MedicineSubstructureHydrophobic and Hydrophilic InteractionsAlgorithmsSoftwareSAR and QSAR in Environmental Research
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Interactions entre la beta-lactoglobuline et les arômes : impact au niveau moléculaire

2008

Interactions between β-lactoglobulin (BLG) and aroma compounds were investigated by complementary techniques for a better knowledge of binding mechanisms between proteins and aroma compounds at a molecular scale. Two binding sites have been defined for the monomeric BLG, one internal site within the central calyx, and one external site between the calyx and the α helix. In a first step, a relation between the ligand structure and its binding behaviour was established from the study of impact of a wide range of aroma compounds on the structure of native BLG. We evidenced at least two binding behaviours as a function of the chemical class, the hydrophobicity, or the structure of the ligands. …

REARRANGEMENT DE LA STRUCTURESURFACE HYDROPHOBICITY[SPI.GPROC] Engineering Sciences [physics]/Chemical and Process EngineeringRPSSPRINTERACTIONSBETA-LACTOGLOBULINEDCTHERMAL TREATMENTIRTFSITE D'INTERACTIONAROMA COMPOUND[SDV.IDA]Life Sciences [q-bio]/Food engineering[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process EngineeringFLUORESCENCESTRUCTURAL REARRANGEMENTTRAITEMENT THERMIQUE[SDV.IDA] Life Sciences [q-bio]/Food engineeringITCβ-LACTOGLOBULINNMRETAT GLOBULAIRE FONDURMNCDFTIRHYDROPHOBIE DE SURFACEBINDING SITEMOLTEN GLOBULE STATE
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Improvement of the wettability and dissolution of fenofibrate compacts by plasma treatment

2011

Abstract The goal of this study was to investigate the effect of plasma treatment on the wettability and dissolution of fenofibrate compacts. Contact angle measurements and intrinsic dissolution rate studies of untreated and plasma-treated fenofibrate compacts were conducted. The contact angle data clearly show that the wettability of the tablet surface increased with the duration of plasma treatment. Analyses of stability revealed that the surfaces which were plasma-treated for more than 1 min regained some degree of hydrophobicity after storage in air. Since their hydrophobic recovery finally reached the level observed with 1 min plasma-treated fenofibrate compacts it was deduced that per…

Radiation NonionizingMaterials sciencePlasma irradiationFenofibrateChromatographyDrug CompoundingPharmaceutical SciencePlasma treatmentOxygenContact angleFenofibrateSolubilityChemical engineeringWettabilitymedicineWettingSolubilitySaturation (chemistry)Hydrophobic and Hydrophilic InteractionsDissolutionTabletsmedicine.drugInternational Journal of Pharmaceutics
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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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The Tobacco mosaic virus movement protein associates with but does not integrate into biological membranes

2014

Plant positive-strand RNA viruses require association with plant cell endomembranes for viral translation and replication, as well as for intra- and intercellular movement of the viral progeny. The membrane association and RNA binding of the Tobacco mosaic virus (TMV) movement protein (MP) are vital for orchestrating the macromolecular network required for virus movement. A previously proposed topological model suggests that TMV MP is an integral membrane protein with two putative -helical transmembrane (TM) segments. Here we tested this model using an experimental system that measured the efficiency with which natural polypeptide segments were inserted into the ER membrane under conditions…

Recombinant Fusion ProteinsvirusesMolecular Sequence DataImmunologyGene ExpressionMicrobiologiaBiologyEndoplasmic ReticulumMicrobiologyCell membraneGenes ReporterPlant CellsVirologymedicineTobacco mosaic virusAmino Acid SequenceMovement proteinIntegral membrane proteinStructure and AssemblyCell MembraneViral translationfungifood and beveragesBiological membraneVirologyTransmembrane proteinTransport proteinCell biologyVirusPlant Viral Movement ProteinsTobacco Mosaic VirusProtein Transportmedicine.anatomical_structureInsect ScienceHydrophobic and Hydrophilic InteractionsProtein Binding
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Influence of PVP/VA copolymer composition on drug–polymer solubility

2015

In this study, the influence of copolymer composition on drug-polymer solubility was investigated. The solubility of the model drug celecoxib (CCX) in various polyvinylpyrrolidone/vinyl acetate (PVP/VA) copolymer compositions (70/30, 60/40, 50/50 and 30/70 w/w) and the pure homopolymers polyvinylpyrrolidone (PVP) and polyvinyl acetate (PVA) was predicted at 25 °C using a thermal analysis method based on the recrystallization of a supersaturated amorphous dispersion (recrystallization method). These solubilities were compared with a prediction based on the solubility of CCX in the liquid monomeric precursors of PVP/VA, N-vinylpyrrolidone (NVP) and vinyl acetate (VA), using the Flory-Huggins …

Recrystallization (geology)PolymersChemistry PharmaceuticalPharmaceutical Science02 engineering and technologyFlory–Huggins solution theory030226 pharmacology & pharmacy03 medical and health scienceschemistry.chemical_compound0302 clinical medicineDrug StabilityPolymer chemistrymedicineVinyl acetateCopolymerSolubilityPolyvinyl acetatePolyvinylpyrrolidonePovidone021001 nanoscience & nanotechnologyMonomerSolubilitychemistryCelecoxibThermodynamicsPolyvinylsCrystallization0210 nano-technologyHydrophobic and Hydrophilic Interactionsmedicine.drugEuropean Journal of Pharmaceutical Sciences
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