Search results for "Anions"

showing 10 items of 126 documents

Conductance and Ion Selectivity of a Mesoscopic Protein Nanopore Probed with Cysteine Scanning Mutagenesis

2005

Nanometer-scale proteinaceous pores are the basis of ion and macromolecular transport in cells and organelles. Recent studies suggest that ion channels and synthetic nanopores may prove useful in biotechnological applications. To better understand the structure-function relationship of nanopores, we are studying the ion-conducting properties of channels formed by wild-type and genetically engineered versions of Staphylococcus aureus alpha-hemolysin (alphaHL) reconstituted into planar lipid bilayer membranes. Specifically, we measured the ion selectivities and current-voltage relationships of channels formed with 24 different alphaHL point cysteine mutants before and after derivatizing the c…

AnionsModels MolecularStaphylococcus aureusCell Membrane PermeabilityBacterial ToxinsLipid BilayersAnalytical chemistryBiophysics02 engineering and technologyIonHemolysin ProteinsStructure-Activity Relationship03 medical and health sciencesCationsNanotechnologyCysteineChannels Receptors and Electrical SignalingLipid bilayerIon channel030304 developmental biologyIons0303 health sciencesChemistrySulfhydryl ReagentsConductance021001 nanoscience & nanotechnologyElectrostaticsElectrophysiologyNanoporeMembraneMutagenesisMutagenesis Site-DirectedBiophysicsGenetic Engineering0210 nano-technologySelectivityBiotechnologyBiophysical Journal
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Sterically geared tris-thioureas; transmembrane chloride transporters with unusual activity and accessibility

2015

Tris-N-arylthioureas derived in one step from 1,3,5-tris(aminomethyl)-2,4,6-triethylbenzene are remarkably effective anion carriers. With optimised aryl substituents their activities come close to the best currently known, suggesting that they might find use as readily available standards in anion transport research.

AnionsModels MolecularTrisSteric effectsCrystallography X-RayChlorideCatalysisPhysico-chimie généralechemistry.chemical_compoundChloridesMaterials ChemistrymedicineChimieMoleculeOrganic chemistryta116Ion transporterIon TransportMolecular StructureChemistryArylThioureatransmembrane anion carriersMetals and Alloystransmembrane transportersGeneral ChemistryCombinatorial chemistryTransmembrane proteinSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChimie organiqueThioureaCeramics and Compositesmedicine.drugChemical Communications
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A bis(triazole)benzamide receptor for the complexation of halide anions and neutral carboxylic acid guests. Guest-controlled topicity and self-assemb…

2012

Bis(triazole)benzamide 1 has been readily synthesized by means of Cu-catalyzed 1,3-dipolar cycloaddition and its ability to bind halide anions and neutral gallic acid derivative 12GA has been theoretically and experimentally investigated. The cavity defined by the N-H amide group and the vicinal aromatic hydrogens is suitable to form H-bonding arrays with halide guests. The stability of complexes 1·Cl- and 1·Br- is very similar, as DFT calculations predict and 1H NMR titration experiments confirm. The zigzag "anti" conformation of the molecule generates two regions with complementary positive and negative potentials that favor the statistical complexation of two molecules of the neutral car…

AnionsModels Molecularchemistry.chemical_classificationStereochemistryCarboxylic acidOrganic ChemistryCarboxylic AcidsTriazoleTopicityHalideTriazolesBromineBiochemistryCycloadditionchemistry.chemical_compoundchemistryAmideBenzamidesPolymer chemistryMoleculeChlorinePhysical and Theoretical ChemistryDerivative (chemistry)Org. Biomol. Chem.
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Bis(5-tert-butyl-2-hydroxy-3-methylbenzyl)(6-hydroxyhexyl)ammonium chloride monohydrate, an anion receptor complex

2007

In the title compound, C(30)H(48)NO(3)(+) x Cl(-) x H(2)O, the cation acts with a water molecule as a chloride ion receptor. The chloride ion forms three strong intramolecular hydrogen bonds. The water molecule forms both an intramolecular bridge between one phenol H atom and the chloride ion, and an intermolecular link to the aliphatic alcohol O atom. Weak intermolecular C-H...Cl and C-H ...O hydrogen bonds provide additional packing interactions.

AnionsModels Molecularinorganic chemicalsBenzylaminesStereochemistryChemistryHydrogen bondIntermolecular forceHydrogen BondingGeneral MedicineCrystallography X-RayChlorideMedicinal chemistryAmmonium ChlorideGeneral Biochemistry Genetics and Molecular BiologyIonchemistry.chemical_compoundIntramolecular forcemedicineMoleculePhenolAmmonium chloridemedicine.drugActa Crystallographica Section C Crystal Structure Communications
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Anion-Exchange Properties of Trifluoroacetate and Triflate Salts of N-Alkylammonium Resorcinarenes

2016

The synthesis of N-benzyl- and N-cyclohexylammonium resorcinarene trifluoroacetate (TFA) and triflate (OTf) salt receptors was investigated. Solid-state analysis by single-crystal X-ray diffraction revealed that the N-alkylammonium resorcinarene salts (NARSs) with different upper substituents had different cavity sizes and different affinities for anions. Anion-exchange experiments by mixing equimolar amounts of N-benzylammonium resorcinarene trifluoroacetate and N-cyclohexylammonium resorcinarene triflate, as well as N-benzylammonium resorcinarene triflate and N-cyclohexylammonium resorcinarene trifluoroacetate showed that the NARS with flexible benzyl groups preferred the larger OTf anion…

AnionsModels MolecularsaltsPhenylalanineElectrospray ionizationInorganic chemistrySalt (chemistry)Benzylammonium CompoundsCrystallography X-Ray010402 general chemistryCrystal engineeringchemistry01 natural sciencesBiochemistryIonDioxanesX-rayPolymer chemistryTrifluoroacetic AcidAnion bindingta116N-AlkylammoniumMesylateschemistry.chemical_classificationanion-exchangeIon exchange010405 organic chemistryChemistryOrganic ChemistryGeneral ChemistryResorcinarene3. Good health0104 chemical sciencesCalixarenesTrifluoromethanesulfonateChemistry: An Asian Journal
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Facilitated Anion Transport Induces Hyperpolarization of the Cell Membrane That Triggers Differentiation and Cell Death in Cancer Stem Cells

2015

Facilitated anion transport potentially represents a powerful tool to modulate various cellular functions. However, research into the biological effects of small molecule anionophores is still at an early stage. Here we have used two potent anionophore molecules inspired in the structure of marine metabolites tambjamines to gain insight into the effect induced by these compounds at the cellular level. We show how active anionophores, capable of facilitating the transmembrane transport of chloride and bicarbonate in model phospholipid liposomes, induce acidification of the cytosol and hyperpolarization of plasma cell membranes. We demonstrate how this combined effect can be used against canc…

AnionsPHPhysiologyCellular differentiationTRANSMEMBRANE TRANSPORTChemistry OrganicFisiologiaPROGRESSIONApoptosisNanotechnologyStem cellsBiochemistryCatalysisCell LineMembrane PotentialsCell membraneColloid and Surface ChemistryCancer stem cellBINDINGPathologymedicineHumansSYNTHETIC ION CHANNELSMembrane potentialIon TransportANALOGSChemistryCHLORIDE TRANSPORTCell MembraneApoptosiQuímica orgánicaCell DifferentiationMICROBIOLOGIAGeneral ChemistryHyperpolarization (biology)Membrane transportCARRIERSPatologiaAPOPTOSISCell biologyCytosolmedicine.anatomical_structureLiposomesCancer cellNeoplastic Stem CellsCèl·lules mareJournal of the American Chemical Society
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Synthesis, Structure and Anion Sensing Properties of a Dicationic Bis(imidazolium)-Based Cyclophane

2018

The preparation and sensing properties of a tetracyclic cyclophane receptor containing two imidazolium rings as anion binding sites and two fluorene rings as fluorescent signaling units, are reported. The receptor behaves as a selective fluorescent chemosensor molecule for inorganic phosphates. H-NMR spectroscopical data clearly indicate the simultaneous occurrence of charge-assisted aromatic and aliphatic C−H noncovalent interactions. PCM/DFT calculations have been carried out to predict the structures of the complexes formed with one and two molecules of PF , HPO and HPO .

AnionsPhysics010405 organic chemistryGeneral Chemistry010402 general chemistry01 natural sciencesMedicinal chemistryHydrogen bonds0104 chemical scienceschemistry.chemical_compoundchemistryImidazoliumCyclophaneSensorCyclophaneChemistrySelect
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Thermo-responsive hydrogels from cellulose-based polyelectrolytes and catanionic vesicles for biomedical application.

2016

In this study, negatively charged catanionic vesicles/hydrophobically modified hydroxyethylcellulose polymers thermo-responsive hydrogels have been fabricated. Vesicular aggregates were found to act as multifunctional junctions for networking of modified-cellulose water solutions. The contributions of the electrostatic and hydrophobic interactions were evaluated by changing either vesicles composition or the polymer hydrophobic substitution. Thermal-induced size and lamellarity of hydrogel-enclosed vesicles were detected, with further polygonal shape changes induced by cellulose-based polymer addition. The thermal transition was also found to tune hydrogel mechanical behaviour. The network …

AnionsProton Magnetic Resonance SpectroscopyBiomedical EngineeringBiomedical TechnologyCeramics and CompositeBiomaterialsDiffusioncatanionic vesicleTheophyllineCationsCellulosecatanionic vesicles; cellulose; diffusion; hydrogel; NMR; rheology; Ceramics and Composites; Biomaterials; Biomedical Engineering; 2506ViscositydiffusionTemperatureHydrogelsBiomaterialPolyelectrolytescelluloseNMRElasticityDrug LiberationSettore CHIM/09 - Farmaceutico Tecnologico Applicativocatanionic vesiclesCeramics and Compositesrheologyhydrogel2506RheologyJournal of biomedical materials research. Part A
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N-Propyl-N′-2-pyridylurea-modified silica as mixed-mode stationary phase with moderate weak anion exchange capacity and pH-dependent surface charge r…

2018

Herein, we present a novel silica-based stationary phase modified with N-propyl-N'-2-pyridylurea selector. Due to the weakly basic properties of the pyridine selector and the presence of residual silanols after selector immobilization, a zwitterionic surface with a pI observed at approximately pH 5.5 was measured by electrophoretic light scattering in pH-dependent ζ-potential determinations. The capability of the new N-propyl-N'-2-pyridylurea-modified silica to serve as mixed-mode stationary phase was investigated. For this purpose, it was characterized under RP and HILIC conditions using test mixtures. Subsequent classification of this stationary phase in comparison to in-house and commerc…

AnionsPyridinesSurface PropertiesSilicon dioxideAnalytical chemistryUridine Triphosphate02 engineering and technology01 natural sciencesBiochemistryUridine DiphosphateAnalytical Chemistrychemistry.chemical_compoundUreaSurface chargeAnion Exchange ResinsChromatographyIon exchangeChemistryElutionHydrophilic interaction chromatography010401 analytical chemistryOrganic ChemistryGeneral MedicineHydrogen-Ion ConcentrationChromatography Ion ExchangeSilicon Dioxide021001 nanoscience & nanotechnology0104 chemical sciencesMixed-mode chromatographyElectrophoretic light scatteringUridine Monophosphate0210 nano-technologySelectivityHydrophobic and Hydrophilic InteractionsJournal of Chromatography A
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The Radical Trap in Atom Transfer Radical Polymerization Need Not Be Thermodynamically Stable. A Study of the MoX3(PMe3)3 Catalysts

2005

The molybdenum(III) coordination complexes MoX(3)(PMe(3))(3) (X = Cl, Br, and I) are capable of controlling styrene polymerization under typical atom transfer radical polymerization (ATRP) conditions, in conjunction with 2-bromoethylbenzene (BEB) as an initiator. The process is accelerated by the presence of Al(OPr(i))(3) as a cocatalyst. Electrochemical and synthetic studies aimed at identifying the nature of the spin trap have been carried out. The cyclic voltammogram of MoX(3)(PMe(3))(3) (X = Cl, Br, I) shows partial reversibility (increasing in the order ClBrI) for the one-electron oxidation wave. Addition of X(-) changes the voltammogram, indicating the formation of MoX(4)(PMe(3))(3) f…

AnionsReaction mechanismRadical polymerization010402 general chemistryPhotochemistry01 natural sciencesBiochemistryRedoxCatalysisStyreneCatalysisStyreneschemistry.chemical_compoundColloid and Surface ChemistryRadical polymerizationOxidationOrganic chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryRedox reactions010405 organic chemistryAtom-transfer radical-polymerizationGeneral Chemistry[CHIM.CATA]Chemical Sciences/Catalysis0104 chemical sciences[CHIM.POLY]Chemical Sciences/PolymersPolymerizationchemistryCyclic voltammetry
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