Search results for "Monomer"

showing 10 items of 857 documents

Comparative Study of the Mechanical Unfolding Pathways of α- and β-Peptides

2015

Using molecular simulations, we analyze the unfolding pathways of various peptides. We compare the mechanical unfolding of a β-alanine's octamer (β-HAla8) and an α-alanine's decamer (α-Ala10). Using force-probe molecular-dynamics simulations, to induce unfolding, we show that the 3(14)-helix formed by β-HAla8 is mechanically more stable than the α-helix formed by α-Ala10, although both structures are stabilized by six hydrogen bonds. Additionally, computations of the potential of mean force validate this result and show that also the thermal stability of the 3(14)-helix is higher. It is demonstrated that β-HAla8 unfolds in a two-step fashion with a stable intermediate. This is contrasted wi…

Dynamic strengthHydrogen bondHydrogen BondingMolecular Dynamics SimulationProtein Structure SecondarySurfaces Coatings and Filmschemistry.chemical_compoundCrystallographyMonomerchemistrybeta-AlanineMaterials ChemistryBiophysicsThermal stabilityHistone octamerPhysical and Theoretical ChemistryPotential of mean forcePeptidesThe Journal of Physical Chemistry B
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Partial Reduction and Selective Transfer of Hydrogen Chloride on Catalytic Gold Nanoparticles

2017

© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim HCl in solution accepts electron density from Au NPs and partially reduces at room temperature, as occurs with other simple diatomic molecules, such as O2 and H2. The activation can be run catalytically in the presence of alkynes to give exclusively E-vinyl chlorides, after the regio- and stereoselective transfer of HCl. Based also on this method, vinyl chloride monomer (VCM) can be produced in a milder and greener way than current industrial processes.

Electron densityInorganic chemistryhydrochlorinationPhotochemistry010402 general chemistryalkynes01 natural sciencesCatalysisVinyl chlorideCatalysischemistry.chemical_compoundvinyl chloridesHydrogen chloride010405 organic chemistryOrganic ChemistryGeneral ChemistryGeneral MedicinegoldDiatomic molecule0104 chemical sciencesMonomerheterogeneous catalysischemistryColloidal goldChemical SciencesStereoselectivity
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Antibacterial studies, DNA oxidative cleavage, and crystal structures of Cu(II) and Co(II) complexes with two quinolone family members, ciprofloxacin…

2005

Nine coordination compounds of Cu(II) and Co(II) with Ciprofloxacin (HCp) and Enoxacin (HEx) as ligands have been prepared and characterized. Single crystal structural determinations of [Cu(HCp)2(ClO4)2].6H2O (1) and [Co(HEx)2(Ex)]Cl.2CH(3)OH.12H2O (4) are reported. The crystal of 1 is composed of [Cu(HCp)2(ClO4)2] units with the two perchlorate anions semicoordinated, and uncoordinated water molecules. The copper ion, at a crystallographic inversion centre, is in a tetragonally distorted octahedral environment. The structure of 4 consists of cationic monomeric [Co(HEx)2(Ex)]+ units, chloride anions, and uncoordinated methanol and water molecules. The complex is six-coordinate, with a sligh…

EnoxacinStereochemistryCrystal structureQuinolonesCrystallography X-RayGram-Positive BacteriaLigandsBiochemistryCoordination complexInorganic Chemistrychemistry.chemical_compoundPerchlorateAnti-Infective AgentsCiprofloxacinCationsGram-Negative BacteriaOrganometallic CompoundsEnoxacinmedicineMoleculeCiprofloxacin HydrochlorideBond cleavageElectrophoresis Agar Gelchemistry.chemical_classificationMolecular StructureCobaltDNAMonomerchemistryOxidation-ReductionCoppermedicine.drugJournal of Inorganic Biochemistry
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Oxidation of diclofenac in the presence of iron(II) octacarboxyphthalocyanine

2021

Abstract This paper presents the results of the research on the influence of catalytic activity of iron(II) octacarboxyphthalocyanines (FePcOC) on the transformation of diclofenac (DCF) which is the most popular anti-inflammatory analgesic. Diclofenac poses a serious threat to the natural environment. The paper demonstrates that diclofenac, in the presence a monomeric form of iron octacarboxyphthalocyanine and hydroxyl radicals (HO•) (from H2O2), undergoes a transformation into diclofenac-2,5-iminoquinone (DCF-2,5-IQ), causing distinct changes in the UV–Vis absorption spectrum. In the presence of iron octacarboxyphthalocyanine and H2O2, the previously colourless diclofenac solution becomes …

Environmental EngineeringDiclofenacAbsorption spectroscopyIronHealth Toxicology and MutagenesisRadical0208 environmental biotechnology02 engineering and technology010501 environmental sciencesDFT calculations01 natural sciencesHigh-performance liquid chromatographyCatalysischemistry.chemical_compoundDiclofenacmedicineEnvironmental ChemistryFerrous Compounds0105 earth and related environmental sciencesMS analysisHplc analysisChemistryPublic Health Environmental and Occupational HealthMs analysisHydrogen PeroxideGeneral MedicineGeneral ChemistryUV–Vis spectraPollution020801 environmental engineeringTD-DFT spectraMonomerIron octacarboxyphthalocyanineHPLCOxidation-ReductionNuclear chemistrymedicine.drugChemosphere
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A model for the formation and degradation of bound residues of the herbicide 14C-isoproturon in soil

1999

Abstract The humic monomer catechol was reacted with 14 C-isoproturon and some of its metabolites, including 14 C-4-isopropylaniline, in aqueous solution under a stream of oxygen. Only in the case of 14 C-4-isopropylaniline, incorporation in oligomers, in fulvic acid-like polymers, and in humic acid-like polymers was observed. The main oligomer was identified by mass spectrometry as 4,5-bis-(4-isopropylphenylamino)-3,5-cyclohexadiene-1,2-dione. Oligomers and polymers containing bound 14 C-4-isopropylaniline were subjected to biodegradation studies in a loamy agricultural soil during 55 days by quantifying 14 CO 2 evolved. In all cases, significant mineralization rates could be determined, w…

Environmental EngineeringHealth Toxicology and MutagenesisOligomerchemistry.chemical_compoundSoil PollutantsEnvironmental ChemistryHumic acidOrganic matterCarbon RadioisotopesHumic Substanceschemistry.chemical_classificationMethylurea CompoundsAqueous solutionHerbicidesPhenylurea CompoundsPesticide ResiduesPublic Health Environmental and Occupational HealthGeneral MedicineGeneral ChemistryMineralization (soil science)BiodegradationPollutionSoil contaminationBiodegradation EnvironmentalMonomerchemistryEnvironmental chemistryChemosphere
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Interaction of the Vibrio cholerae cytolysin (VCC) with cholesterol, some cholesterol esters, and cholesterol derivatives: a TEM study.

2002

The Vibrio cholerae cytolysin (VCC) 63-kDa monomer has been shown to interact in aqueous suspension with cholesterol microcystals to produce a ring/pore-like heptameric oligomer approximately 8 nm in outer diameter. Transmission electron microscopy data were produced from cholesterol samples adsorbed to carbon support films, spread across the holes of holey carbon films, and negatively stained with ammonium molybdate. The VCC oligomers initially attach to the edge of the stacked cholesterol bilayers and with increasing time cover the two planar surfaces. VCC oligomers are also released into solution, with some tendency to cluster, possibly via the hydrophobic membrane-spanning domain. At th…

ErgosterolLiposomeCytotoxinsTemperatureOligomerNegative stainProtein Structure TertiaryCrystallographychemistry.chemical_compoundMicroscopy ElectronMonomerCholesterolchemistryPulmonary surfactantModels ChemicalStructural BiologySide chainImage Processing Computer-Assistedlipids (amino acids peptides and proteins)CytolysinCholesterol EstersVibrio choleraeFluorescent DyesJournal of structural biology
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Oligomerization and hemolytic properties of the C-terminal domain of pyolysin, a cholesterol-dependent cytolysin

2013

Pyolysin (PLO) belongs to the homologous family of the cholesterol- dependent cytolysins (CDCs), which bind to cell membranes containing cholesterol to form oligomeric pores of large size. The CDC monomer structure consists of 4 domains. Among these, the C-terminal domain 4 has been implicated in membrane binding of the monomer, while the subsequent processes of oligomerization and membrane insertion have primarily been assigned to other domains of the molecule. Recombinantly expressed or proteolytic fragments that span domain 4 of the CDCs streptolysin O and perfringolysin O bind to membranes but fail to oligomerize, and they inhibit the activity of the respective wild-type toxins. We repo…

ErythrocytesMembrane bindingCellprotein bindingBiochemistryoligomerHemolysin Proteinschemistry.chemical_compoundReaction kineticsToxic materialsMonomersprotein domainRecombinant ProteinsHemolysisunclassified drugcytolysinmedicine.anatomical_structureMembraneBiochemistryStreptolysinsStreptolysinLarge sizeBacterial ToxinsBiologyCholesterol-dependent cytolysinHemolysisoligomerizationMembrane LipidsBacterial ProteinsProteolytic fragmentsEscherichia colimedicineAnimalsMonomer structuresMolecular BiologySheep Domesticcarboxy terminal sequenceC-terminal domainsCholesterolC-terminusCell MembraneHemolytic activitycholesterolCell Biologymedicine.diseaseProtein Structure TertiaryCell membranesKineticschemistryOligomersProtein MultimerizationPyolysinprotein pyolysinMembrane insertionCytology
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Electrophoretic separation of a class of nucleosomes enriched in HMG 14 and 17 and actively transcribed globin genes.

1980

Monomer nucleosomes from chick erythrocytes can be fractionated according to their electrophoretic mobility in (comparatively) high salt acrylamide gels. We show that the fractionation is based predominantly on differences in charge. The monomer heterogeneity persists even when the nucleosomes are trimmed down to 145 bp with Exo III or when H1 and H5 are removed. The slowest migrating monomers are associated with HMG 14 and 17; however, we do not believe that these proteins are entirely responsible for the altered mobility since the nucleosome heterogeneity persists even after removal of HMG 14 and 17. The DNA associated with the HMG 14 and 17 containing nucleosomes is shown to be enriched …

ErythrocytesbiologyChromosomal Proteins Non-HistoneHigh Mobility Group ProteinsCell FractionationNucleosomesHistoneschemistry.chemical_compoundElectrophoresisMonomerHistonechemistryBiochemistryHMG-CoA reductaseGeneticsbiology.proteinNucleosomeAnimalsElectrophoresis Polyacrylamide GelGlobinCell fractionationChickensDNA
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Spectroscopic studies of 5,5′-dimethoxy-3,3,′-disulfobutyl-9-ethylthiacarbocyanine (DDTC) in solutions and immobilized in sol-gel matrices

1998

Abstract Absorption spectra of 5,5′-dimethoxy-3,3,′-disulfobutyl-9-ethylthiacarbocyanine (DDTC) in aqueous solutions and immobilized in xerogels prepared by the sol-gel method were obtained. Influence of pH, detergent (Triton X-100), ethanol addition and sol-gel preparation method on the dye aggregation equilibria and its photostability were investigated. In liquid solutions lowering of pH, as well as addition of the detergent, shift the aggregation equilibrium towards the DDTC monomeric form. However, while more acidic conditions result in a decrease of the dye stability, addition of the detergent has a slightly stabilizing effect on the dye. However, addition of ethanol drastically reduce…

EthanolAqueous solutionAbsorption spectroscopyChemistryDimerOrganic ChemistryDopingInorganic chemistryAnalytical ChemistryInorganic ChemistryPreparation methodchemistry.chemical_compoundMonomerSpectroscopySol-gelJournal of Molecular Structure
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From an epoxide monomer toolkit to functional PEG copolymers with adjustable LCST behavior.

2011

The lower critical solution temperature (LCST) behavior of novel poly(ethylene glycol) (PEG)-based copolymers bearing multiple functional groups, obtained by anionic ring-opening (co)polymerization (AROP), has been investigated. Variable comonomer ratios of ethylene oxide (EO) and the corresponding oxiranes isopropylidene glyceryl glycidyl ether (IGG), ethoxyl vinyl glycidyl ether (EVGE), allyl glycidyl ether (AGE), or N,N-dibenzyl amino glycidyl (DBAG), particularly designed to implement functional groups at the PEG backbone, were found to influence the LCST behavior. Sharp transitions from translucent to opaque solutions, comparable to other well-established stimuli-responsive polymers, w…

Ethylene OxideMaterials scienceHot TemperaturePolymers and PlasticsPolymersAllyl glycidyl etherpolyethersEpoxideLower critical solution temperaturePolymerizationPolyethylene Glycolschemistry.chemical_compoundPolymer chemistrycopolymersMaterials ChemistryCopolymerPoly(Ethylene Glycol) CopolymersSide-ChainsAqueous-SolutionEthylene oxideComonomerstimuli-sensitiveOrganic ChemistryPegchemistryPolymerizationGlycidolLcstEthylene glycolHydrophobic and Hydrophilic InteractionsMacromolecular rapid communications
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