Search results for "affinity"

showing 10 items of 313 documents

Characterization of aquatic humic substances and their metal complexes by immobilized metal-chelate affinity chromatography on iron(III)-loaded ion e…

2001

The analytical fractionation of aquatic humic substances (HS) by means of immobilized metal-chelate affinity chromatography (IMAC) on metal-loaded chelating ion exchangers is described. The cellulose HYPHAN, loaded with different trivalent ions, and the chelate exchanger Chelex 100, loaded to 90% of its capacity with Fe(III), were used. The cellulose HYPHAN, loaded with 2% Fe(III), resulted in HS distribution coefficients Kd of up to 10(3.7) mL/g at pH 4.0 continuously decreasing down to 10(1.5) at pH 12, which were appropriate for HS fractionation by a pH-depending chromatographic procedure. Similar distribution coefficients Kd were obtained for HS sorption onto Fe(III)-loaded Chelex 100. …

chemistry.chemical_classificationChromatographyIon exchangeElutionIronSorptionFractionationReference StandardsChromatography Ion ExchangeBiochemistryChromatography Affinitychemistry.chemical_compoundChelex 100chemistryMetalsSpectroscopy Fourier Transform InfraredHumic acidSpectrophotometry UltravioletChelationCelluloseHumic SubstancesWater Pollutants ChemicalChelating AgentsFresenius' Journal of Analytical Chemistry
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A theoretical study of neutral and reduced tetracyano-p-quinodimethane (TCNQ)

2004

Abstract The molecular structure of neutral, anionic, and dianionic tetracyano- p -quinodimethane (TCNQ), as well as the electron affinity of TCNQ, have been studied with HF, MP2, and different density functional theory (DFT) procedures. The optimized geometries compare well with the available experimental data, although the C N bond distance is not correctly described at the MP2 level. The calculated parameters are rather insensitive to the basis set employed, and the addition of diffuse functions does not yield significant changes. When the extra electrons are added, the central ring of TCNQ progressively becomes more aromatic. Compared with the CCSD(T) estimate, the value of the adiabati…

chemistry.chemical_classificationElectron acceptorCondensed Matter PhysicsBiochemistryBond lengthMolecular geometrychemistryComputational chemistryYield (chemistry)Electron affinityMoleculePhysical chemistryDensity functional theoryPhysical and Theoretical ChemistryBasis setJournal of Molecular Structure: THEOCHEM
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Binding and isomerization energies for the Cu/CN and Cu(I)CN interactions

1993

Abstract Binding and isomerization energies of the CuCN, CuNC, CuCN+, and CuNC+ systems were investigated by means of a multireference CI perturbatively selected, MRCI-PS approach. The inclusion of the main dynamical correlation effects are evaluated. The binding energies for CuCN and CuNC are 4.37 and 4.03 eV, respectively, and those for CuCN+ and CuNC+ are 0.08 and 1.61 eV. Calculated isomerization energies are 7.86 and 35.98 kcal/mol for CuCN and Cu(I)CN isomerizations, respectively.

chemistry.chemical_classificationElectronic correlationBinding energyGaussian orbitalGeneral Physics and AstronomyConfiguration interactionBond-dissociation energyCrystallographychemistryComputational chemistryElectron affinityPhysical and Theoretical ChemistryInorganic compoundIsomerizationChemical Physics
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Hierarchical Imprinting Using Crude Solid Phase Peptide Synthesis Products as Templates

2003

The crude products resulting from solid-phase peptide synthesis can be used as epitope templates to generate surface-confined sites for the template and larger peptides containing the template motif. This offers a facile route to robust affinity stationary phases for the chromatographic separation of peptides.

chemistry.chemical_classificationGeneral Chemical EngineeringPeptideGeneral ChemistryEpitopechemistry.chemical_compoundChromatographic separationTemplateAffinity chromatographychemistryMaterials ChemistryPeptide synthesisOrganic chemistryImprinting (psychology)Molecular imprintingChemistry of Materials
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3,3'-Bicarbazole structural derivatives as charge transporting materials for use in OLED devices

2018

In this study we report novel 3,3′-bicarbazole based charge transporting materials mainly designed for a use in systems containing phosphorescent iridium (III) complex emitters. A low-cost oxidative coupling reaction using FeCl3 was employed in the synthesis of 3,3′-bicarbazole compounds. Different derivatives of 3,3′-bicarbazole with 4-ethoxyphenyland ethyl- substituents at 9,9′- positions and (2,2-diphenylhydrazono)methyl- and 4-(dimethylamino)styryl- substituents at 6,6′- positions were synthesized. Obtained (2,2-diphenylhydrazono)methyl- derivatives exhibit glass transition temperatures that are sufficient for applications in electronic devices. Thin amorphous films of good optical qual…

chemistry.chemical_classificationMaterials sciencechemistryElectron affinityOLEDPhysical chemistrychemistry.chemical_elementMoleculeIridiumElectron acceptorGlass transitionPhosphorescenceAmorphous solidOrganic Electronics and Photonics: Fundamentals and Devices
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Photoaffinity cross-linking of F1ATPase from the thermophilic bacterium PS3 by 3′-arylazido-β-alanyl-2-azido ATP

1989

AbstractThe photoactivatable bifunctional 3′-arylazido-β-alanyl-2-azido ATP (2,3′-DiN3ATP) has been applied to study the localization of the nucleotide-binding sites of coupling factor 1 (F1ATPase, TF1) from the thermophilic bacterium PS3 by photoaffinity cross-linking. UV irradiation of TF1 in the presence of 2,3′-DiN3ATP results in the nucleotide-dependent formation of various higher molecular mass cross-links formed by two, three or even four α- and/or β-subunits. The differences observed upon photoaffinity cross-linking by the bifunctional 2-azido ATP or 8-azido ATP analog are discussed. They are probably due to the varied maximal distance between both azido groups, or to the different …

chemistry.chemical_classificationMolecular massbiologyStereochemistryProtein subunitNucleotide conformationBiophysicsCell Biologybiology.organism_classificationBiochemistrychemistry.chemical_compoundEnzymechemistryStructural BiologyGeneticsPhotoaffinity crosslinkingATPase F1-NucleotideNucleotide-binding siteBinding siteBifunctionalInterfacial localizationMolecular BiologyThermophilic bacterium PS3BacteriaFEBS Letters
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Photoaffinity labeling of the coupling factor 1 from the thermophilic bacterum PS3 by 8-azido ATP

1984

AbstractTo localize the nucleotide binding sites of the F1ATPase (TF1) from the thermophilic bacterium PS3 we have used 14C-labeled 8-azido ATP (8-N3ATP) as photoaffmity label. 8-N3ATP is hydrolyzed by the F,ATPase in the absence of ultraviolet light. Irradiation by ultraviolet light of the enzyme in the presence of 8-N3ATP results in reduction of ATPase activity and in preferential nucleotide specific labeling of the α subunits (0.8–0.9 mol 8-N3ATP/TF1,α:β = 4:1). Inactivation and labeling do not depend on the presence of Mg2+. Both effects decrease upon addition of various nucleotide di- or triphosphates.

chemistry.chemical_classificationPhotoaffinity labelingStereochemistryNoncatalytic nucleotide binding siteThermophileBiophysicsCell BiologyBiochemistryCoupling (electronics)HydrolysisEnzymechemistryStructural BiologyPhotoaffinity labelingMoleBacterial F1ATPaseGeneticsUltraviolet lightCatalytic nucleotide binding siteNucleotideThermophilic bacterium PS3Molecular BiologyFEBS Letters
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Validation strategies for antibodies targeting modified ribonucleotides

2020

Chemical modifications are found on almost all RNAs and affect their coding and noncoding functions. The identification of m6A on mRNA and its important role in gene regulation stimulated the field to investigate whether additional modifications are present on mRNAs. Indeed, modifications including m1A, m5C, m7G, 2′-OMe, and Ψ were detected. However, since their abundances are low and tools used for their corroboration are often not well characterized, their physiological relevance remains largely elusive. Antibodies targeting modified nucleotides are often used but have limitations such as low affinity or specificity. Moreover, they are not always well characterized and due to the low abun…

chemistry.chemical_classificationRegulation of gene expression0303 health sciencesMessenger RNAbiologyNucleotidesmedicine.drug_class030302 biochemistry & molecular biologyMethodComputational biologyRibonucleotidesMonoclonal antibodyAntibodies03 medical and health sciencesLow affinitychemistrybiology.proteinmedicineRNANucleotideRNA MessengerAntibodyMolecular Biology030304 developmental biologyRNA
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Stilbenoid phosphors with increased electron affinity: sulfones as electron accepting groups

2001

Stilbenoid compounds are one of the preferred classes of luminescent materials for the use in light emitting diodes (LEDs). A problem connected with the use of poly(phenylenevinylene) (PPV) in LEDs is the unbalanced charge carrier transport, electron injection from aluminium and electron transport properties are only poor. The substitution with electron accepting groups like nitriles is a suitable way to lower the LUMO level of the chromophore. The electron withdrawing strength of sulfones is comparable to cyanides and the second binding site is useful to attach solubilising side chains. A two-step synthesis of model compounds and polymers from ethene and sulfonyl dibromobenzene and bromo a…

chemistry.chemical_classificationSulfonylMechanical EngineeringMetals and AlloysPolymerChromophoreCondensed Matter PhysicsPhotochemistryElectron transport chainElectronic Optical and Magnetic MaterialschemistryMechanics of MaterialsElectron affinityPolymer chemistryMaterials ChemistrySide chainPolar effectHOMO/LUMOSynthetic Metals
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Predicted secondary structure of hydroperoxide lyase from green bell pepper cloned in the yeast Yarrowia lipolytica

2010

International audience; Fatty acid hydroperoxide lyase (HPL) is a member of the cytochrome P450 family acting on fatty acid hydroperoxides in many organisms. The active green bell pepper HPL, cloned and expressed in the yeast Yarrowia lipolytica, was purified by immobilized metal-ion affinity chromatography (IMAC) in the presence of 2% of Triton X-100R. The secondary structure prediction by bioinformatics servers of HPL was realized by ANTHEPROT software, using the GOR, DPM and Predator methods. The theoretical results which are average values obtained from three different calculation methods showed 33% α-helix, 18% β-sheet, 7% turn and 42% coil. On the other hand, the secondary structure a…

chemistry.chemical_classificationYarrowia lipolyticaCircular dichroismChromatographybiologyProcess Chemistry and Technology[SDV]Life Sciences [q-bio]Circular dichroism spectroscopyBioengineeringYarrowiabiology.organism_classificationBiochemistryCatalysisYeastRandom coilHydroperoxide lyaseEnzymeAffinity chromatographyBiochemistrychemistrySecondary structureSpecific activityPredictionProtein secondary structure
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