Search results for " Ion exchange"

showing 10 items of 65 documents

Purification of hydroperoxide lyase from green bell pepper (Capsicum annuum L.) fruits for the generation of C6-aldehydes in vitro.

2002

The aim of this work was to compare the efficiency of different extracts of hydroperoxide lyase from green bell peppers in producing aldehydes: a crude extract, a chloroplastic fraction, and a purified enzyme were investigated. From a crude extract, the HPO lyase was purified by ion-exchange chromatography with a 22.3-fold increase in purification factor. Analysis by SDS-PAGE electrophoresis under denaturating conditions showed only one protein with a molecular weight of 55 kDa, whereas size-exclusion chromatography indicated a molecular weight of 170 kDa. A maximum of 7500 mg of aldehydes per g of protein was obtained with the purified enzyme within 20 min of bioconversion compared to 392 …

Lipid PeroxidesProtein DenaturationChloroplastsLinolenic AcidsBioconversionBiologyAldehydechemistry.chemical_compoundBiosynthesisCytochrome P-450 Enzyme SystemPolyacrylamide gel electrophoresisAldehyde-Lyaseschemistry.chemical_classificationAldehydesChromatographyPlant ExtractsGeneral ChemistryLyasebiology.organism_classificationChromatography Ion ExchangeChloroplastMolecular WeightEnzymechemistryBiochemistryLinoleic AcidsChromatography GelElectrophoresis Polyacrylamide GelGeneral Agricultural and Biological SciencesCapsicumSolanaceaeJournal of agricultural and food chemistry
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Tyrosinases from crustaceans form hexamers

2002

Tyrosinases, which are widely distributed among animals, plants and fungi, are involved in many biologically essential functions, including pigmentation, sclerotization, primary immune response and host defence. In the present study, we present a structural and physicochemical characterization of two new tyrosinases from the crustaceans Palinurus elephas (European spiny lobster) and Astacus leptodactylus (freshwater crayfish). In vivo, the purified crustacean tyrosinases occur as hexamers composed of one subunit type with a molecular mass of approx. 71kDa. The tyrosinase hexamers appear to be similar to the haemocyanins, based on electron microscopy. Thus a careful purification protocol was…

Macromolecular SubstancesProtein subunitTyrosinasePalinurus elephasAstacoideaBiologyAstacus leptodactylusBiochemistryEvolution MolecularSpecies SpecificityCrustaceaHemolymphAnimalsMolecular BiologyMolecular massMonophenol MonooxygenaseEcologyCell BiologyChromatography Ion Exchangebiology.organism_classificationCrayfishKineticsMicroscopy ElectronBiochemistryArthropodSpiny lobsterResearch ArticleBiochemical Journal
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5-Methoxyuridine, a new modified constituent in tRNAs of Bacillaceae.

1976

Magnetic Resonance SpectroscopyBiophysicsBacillusBacillus subtilisMass spectrometryBiochemistryMass Spectrometrychemistry.chemical_compoundRNA TransferSpecies SpecificityStructural BiologyGeneticsMolecular BiologyUridineBacillus (shape)BacillaceaebiologyCell BiologyNuclear magnetic resonance spectroscopyRibonucleotidesbiology.organism_classificationChromatography Ion ExchangeUridinechemistryBiochemistrySpectrophotometry UltravioletBacillus subtilisFEBS letters
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Reversibly stable thiopolyplexes for intracellular delivery of genes.

2006

Novel polyaspartamide non-viral carriers for gene therapy were synthesized by introducing, on the same polymer backbone, positively charged groups, for electrostatic interactions with DNA, and thiol groups for the formation of disulfide bridges between polymer chains. The introduction of thiols was aimed to have a vector with low redox potential sensitivity: disulfide crosslinking in fact, being stable in extracellular environment, allowed either to have stable complexes in plasma, that can protect DNA from metabolism, or to be reduced inside the cell, where the excess of glutathion in reduced form maintains a low redox potential. The consequent destabilization of the complex after disulfid…

Magnetic Resonance SpectroscopyLightStereochemistryCell SurvivalPolymersPharmaceutical ScienceElectrophoretic Mobility Shift AssayGene deliveryTransfectionchemistry.chemical_compoundGene DeliveryMiceDynamic light scatteringGenes ReporterCell Line TumorAnimalsScattering RadiationElectrophoretic mobility shift assayDisulfidesSulfhydryl CompoundsLuciferaseschemistry.chemical_classificationthiopolycationsEndodeoxyribonucleasesLuminescent AgentsGenetic transferCationic polymerizationProteinsDNAChromatography Ion ExchangeCombinatorial chemistrychemistrypolyaspartammideAgarose gel electrophoresisThiolPeptidesOxidation-ReductionDNAJournal of controlled release : official journal of the Controlled Release Society
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The use of high-pressure liquid cation-exchange chromatography for determination of the 5-methylcytosine content of DNA.

1976

MaleChromatographyTroutHydrophilic interaction chromatographyOrganic ChemistryIon chromatographyFishesGeneral MedicineDNAPlantsChromatography Ion ExchangeBiochemistryHigh-performance liquid chromatographySpermatozoaAnalytical Chemistrychemistry.chemical_compound5-MethylcytosineCytosinechemistrySpecies SpecificityHigh pressureMethodsAnimalsDNAChromatography High Pressure LiquidJournal of chromatography
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Conformational Change in the Pheromone-binding Protein fromBombyx mori Induced by pH and by Interaction with Membranes

1999

The pheromone-binding protein (PBP) from Bombyx mori was expressed in Escherichia coli periplasm. It specifically bound radiolabeled bombykol, the natural pheromone for this species. It appeared as a single band both in native and SDS-polyacrylamide gel electrophoresis and was also homogeneous in most chromatographic systems. However, in ion-exchange chromatography, multiple forms sometimes appeared. Attempts to separate them revealed that they could be converted into one another. Analysis of the protein by circular dichroism and fluorescence spectroscopy demonstrated that its tertiary structure was sensitive to pH changes and that a dramatic conformational transition occurred between pH 6.…

MaleConformational changeCircular dichroismSensory Receptor CellsProtein ConformationBiochemistryBombykolchemistry.chemical_compoundEscherichia coliAnimalsDenaturation (biochemistry)Pheromone bindingCloning MolecularMolecular BiologyChemistryCircular DichroismCell BiologyHydrogen-Ion ConcentrationBombyxChromatography Ion ExchangeLigand (biochemistry)Protein tertiary structureProtein Structure TertiarySpectrometry FluorescenceBiochemistryBiophysicsInsect ProteinsIntercellular Signaling Peptides and ProteinsThermodynamicsElectrophoresis Polyacrylamide GelCarrier ProteinsPheromone binding proteinJournal of Biological Chemistry
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Heterogeneity of osteogenesis imperfecta. Biochemical and morphological findings in a case of type III according to Sillence.

1986

A male infant with pale-blue sclerae, who died at the age of 6 weeks through the aspiration of food, presented multiple fractures and deformation of the long tubular bones. The clinical and radiological findings and the course indicated osteogenesis imperfecta, type III, according to Sillence's classification. The family history was unremarkable. Light and electron microscopic studies of iliac crest bone obtained postmortem, showed an abrupt interruption of endochondral ossification, with an active periosteal ossification. In the region of the fractures, a mixed desmochondral callus was seen. The endoplasmic reticulum of the osteoblasts was markedly dilated, the mitochondria were swollen. T…

MaleProlineEndoplasmic ReticulumHydroxylationIliac crestHydroxylysineBone and BonesOsteogenesis Imperfecta Type IIIchemistry.chemical_compoundMedicineHumansAmino AcidsEndochondral ossificationSkinOsteoblastsbusiness.industryOsteoidCartilageInfantAnatomyOsteogenesis Imperfectamedicine.diseaseChromatography Ion ExchangeHydroxylysinemedicine.anatomical_structureCartilagechemistryOsteogenesis imperfectaPediatrics Perinatology and Child HealthCollagenbusinessMitochondrial SwellingReticulumEuropean journal of pediatrics
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Development of HPLC methods for the purification and analysis of plasma membrane glycoproteins.

1990

High resolution HPLC techniques such as affinity chromatography (AC), ion exchange chromatography (IEC), and size exclusion chromatography (SEC) were used successfully for separations of hydrophobic plasma membrane glycoproteins. We have tested a lot of commercially available columns for IEC and SEC and performed the purification of the crude plasma membrane extract with the most suitable columns. By using immobilized ligands with different specificities and sequential affinity chromatography, it is possible to obtain a preliminary structural characterization of the interesting carbohydrate residues of membrane glycoproteins.

Membrane GlycoproteinsChromatographyChemistryHealth Toxicology and MutagenesisHydrophilic interaction chromatographyCell MembraneIon chromatographyPublic Health Environmental and Occupational HealthReversed-phase chromatographyChromatography Ion ExchangeHigh-performance liquid chromatographyDisplacement chromatographyChromatography AffinityAffinity chromatographyEvaluation Studies as TopicProtein purificationChromatography GelHumansChromatography columnChromatography High Pressure LiquidResearch ArticleCell Line TransformedEnvironmental Health Perspectives
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Ultra-short ion-exchange columns for fast charge variants analysis of therapeutic proteins

2021

Abstract The purpose of this work was to study the potential of recently developed ultra-short column hardware for ion exchange chromatography (IEX). Various prototype and commercial columns having lengths of 5, 10, 15, 20 and 50 mm and packed with non-porous 3 µm particles were systematically compared. Both pH and salt gradient modes of elution were evaluated. Similarly, what has been previously reported for reversed phase liquid chromatography (RPLC) mode, an “on-off” retention mechanism was observed in IEX for therapeutic proteins and their fragments (25–150 kDa range). Because of the non-porous nature of the IEX packing material, the column porosity was relatively low (e = 0.42) and the…

Monoclonal antibodyChromatography Reverse-PhaseRange (particle radiation)ddc:615ChromatographyIon exchangeChemistryElutionOrganic ChemistryIon chromatographyIon-exchange chromatographyGeneral MedicineReversed-phase chromatographyChromatography Ion ExchangeBiochemistryUltra-short columnExtra-column volumeAnalytical ChemistryVolume (thermodynamics)PeekPorosityFast separationPorosityChromatography High Pressure Liquid
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Automated multi-dimensional liquid chromatography

2004

A comprehensive on-line sample clean-up with an integrated two-dimensional HPLC system was developed for the analysis of natural peptides. Samples comprised of endogenous peptides with molecular weights up to 20 kDa were generated from human hemofiltrate (HF) obtained from patients with chronic renal failure. The (poly-)peptides were separated using novel silica-based restricted access materials with strong cation-exchange functionalities (SCX-RAM). The size-selective sample fractionation step is followed by cation-exchange chromatography as the first dimension. The subsequent second dimension of separation is based on hydrophobic interaction using four parallel short reversed-phase (RP) co…

PROTEINSClinical BiochemistryMolecular Sequence DataAnalytical chemistryMass spectrometryBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryCIRCULATING HUMAN PEPTIDESColumn chromatographyHumansSample preparationhuman blood filtrateAmino Acid SequenceHUMAN PLASMAPeptide sequenceChromatography High Pressure LiquidChromatographyEdman degradationMolecular masssample preparationChemistryMIXTURESCell BiologyGeneral MedicineReversed-phase chromatographyMASS-SPECTROMETRYENDOSTATINChromatography Ion ExchangeHUMAN HEMOFILTRATEpeptidesSEPARATIONidentificationHPLCFiltrationJournal of Chromatography B-Analytical Technologies in the Biomedical and Life Sciences
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