Search results for "Electrophoresi"

showing 10 items of 1009 documents

Characterizing the interaction between enantiomers of eight psychoactive drugs and highly sulfated-β-cyclodextrin by counter-current capillary electr…

2013

The estimation of apparent binding constants and limit mobilities of the complexes of the enantiomers that characterize the interaction of enantiomers with chiral selectors, in this case highly sulfated β-cyclodextrin, was approached using a simple and economic electrophoretic modality, the complete filling technique (CFT) in counter-current mode. The enantiomers of eight psychoactive drugs, four antihistamines (dimethindene, promethazine, orphenadrine and terfenadine) and four antidepressants (bupropion, fluoxetine, nomifensine and viloxazine) were separated for the first time for this cyclodextrin (CD). Estimations of thermodynamic and electrophoretic enantioselectivies were also performe…

Pharmacologychemistry.chemical_classificationChromatographyCyclodextrinResolution (mass spectrometry)ChemistryClinical BiochemistryGeneral MedicineBiochemistryAnalytical ChemistryPromethazineElectrophoresisCapillary electrophoresisReagentDrug DiscoverymedicineOrphenadrineEnantiomerMolecular Biologymedicine.drugBiomedical Chromatography
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Purification of a nuclease from human serum.

1981

The purification procedure for a nuclease from human serum is described. It includes ammonium sulfate precipitation, chromatography on DEAE-Sephadex and on Sephacryl-S 200, and preparative electrophoresis. The enzyme, purified about 2000-fold, is homogeneous in a sodium dodecyl sulfate electrophoretic system, where it has a mol. wt of 78,000. The pH optimum lies around pH 6.5; it is a sugar-nonspecific endonuclease.

Pharmacologychemistry.chemical_classificationNucleaseChromatographyDeoxyribonucleasesbiologyCell BiologyCellular and Molecular NeuroscienceElectrophoresischemistry.chemical_compoundEndonucleaseKineticsEnzymechemistrybiology.proteinMolecular MedicineHumansAmmoniumSodium dodecyl sulfateSulfateMolecular BiologyAmmonium sulfate precipitationExperientia
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PRK1 phosphorylates MARCKS at the PKC sites: serine 152, serine 156 and serine 163

1996

AbstractThe 80kDa Myristolated Alanine-Rich C-Kinase Substrate (MARCKS) in a major in vivo substrate of protein kinase C (PKC). Here we report that MARCKS is a major substrate for the lipid-activated PKC-related kinase (PRK1) in cell extracts. Furthermore, PRK1 is shown to phosphorylate MARCKS on the same sites as PKC in vitro. Thus, control of MARCKS phosphorylation on these previously identified ‘PKC’ sites may be regulated under certain circumstances by PRK as well as PKC mediated signalling pathways. The implications for MARCKS as a marker of PKC activation and as a point of signal convergence are discussed.

PhosphopeptidesMARCKSPRKRecombinant Fusion ProteinsMolecular Sequence DataBiophysicsKidneyBiochemistryCell-free systemCell LineSerineStructural BiologyProtein kinase CGeneticsAnimalsAmino Acid SequenceBinding siteMARCKSPKCPhosphorylationMyristoylated Alanine-Rich C Kinase SubstrateMolecular BiologyProtein kinase CGlutathione TransferaseBinding SitesCell-Free SystemKinaseChemistryIntracellular Signaling Peptides and ProteinsMembrane ProteinsProteinsCell BiologyHaplorhiniPeptide FragmentsBiochemistryPhosphorylationElectrophoresis Polyacrylamide GelSignal transductionSequence AnalysisSignal TransductionFEBS Letters
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Complement and Atherogenesis

1999

Abstract —Complement activation occurs in temporal correlation with the subendothelial deposition of LDL during early atherogenesis, and complement also plays a pathogenetic role in promoting lesion progression. Two lesion components have been identified that may be responsible for complement activation. First, enzymatic degradation of LDL generates a derivative that can spontaneously activate complement, and enzymatically degraded LDL (E-LDL) has been detected in the lesions. Second, C-reactive protein (CRP) colocalizes with complement C5b-9, as evidenced by immunohistological studies of early atherosclerotic lesions, so the possibility exists that this acute phase protein also fulfills a…

PhosphorylcholineNeuraminidaseComplement Membrane Attack ComplexCoronary Artery DiseaseBiologyPhospholipaseLesionPathogenesismedicineHumansElectrophoresis Gel Two-DimensionalTrypsinComplement Activationchemistry.chemical_classificationPhosphorylcholineC-reactive proteinAcute-phase proteinCholesterol LDLComplement C3Coronary VesselsMolecular biologyComplement systemC-Reactive ProteinEnzymeBiochemistrychemistryType C Phospholipasesbiology.proteinCalciummedicine.symptomCardiology and Cardiovascular MedicineProtein BindingArteriosclerosis, Thrombosis, and Vascular Biology
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Properties of baculovirus particles displaying GFP analyzed by fluorescence correlation spectroscopy.

2003

Abstract Recombinant baculovirus particles displaying green fluorescent protein (GFP) fused to the major envelope glycoprotein gp64 of the Autographa californica multicapsid nucleopolyhedrovirus (AcMNPV) were characterized by fluorescence correlation spectroscopy (FCS). FCS detected Brownian motion of single, intact recombinant baculovirus display particles with a diffusion coefficient (D) of (2.89±0.74)10 8 cm2s 1 and an apparent hydrodynamic radius of 83.35±21.22 nm. In the presence of sodium dodecyl sulfate (SDS), Triton X-100, and octylglucoside, the diffusion time was reduced to the 0.2 ms range (D = 7.5710 7 cm2s 1), showing that the fusion proteins were anchored in the viral envelope…

PhotochemistryvirusesClinical BiochemistryDetergentsGreen Fluorescent ProteinsFluorescence correlation spectroscopySpodopteraBiochemistryGreen fluorescent proteinDiffusionchemistry.chemical_compoundViral envelopeAnimalsSodium dodecyl sulfateMolecular BiologybiologyChemistryViral membranebiology.organism_classificationFluorescenceFusion proteinMolecular biologyMolecular WeightAutographa californicaLuminescent ProteinsSpectrometry FluorescenceElectrophoresis Polyacrylamide GelIndicators and ReagentsBaculoviridaeViral Fusion ProteinsAlgorithmsBiological chemistry
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Computer simulations of single particles in external electric fields

2015

Applying electric fields is an attractive way to control and manipulate single particles or molecules, e.g., in lab-on-a-chip devices. However, the response of nanosize objects in electrolyte solution to external fields is far from trivial. It is the result of a variety of dynamical processes taking place in the ion cloud surrounding charged particles and in the bulk electrolyte, and it is governed by an intricate interplay of electrostatic and hydrodynamic interactions. Already systems composed of one single particle in electrolyte solution exhibit a complex dynamical behaviour. In this review, we discuss recent coarse-grained simulations that have been performed to obtain a molecular-leve…

PhysicsFOS: Physical sciencesGeneral ChemistryElectrolyteCondensed Matter - Soft Condensed MatterCondensed Matter PhysicsCharged particleIonElectrophoresisPolarizabilityChemical physicsElectric fieldParticleSoft Condensed Matter (cond-mat.soft)Constant (mathematics)
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Electrophoretic mobility of charged spheres

2008

The electrophoretic mobility μ of charged 0.3 µm Polystyrene spheres suspended in water was measured over a wide range of salt concentrations c and packing fractions Φ. To observe isolated spheres at packing fractions Φ ≤ 2 × 10−7 a newly developed optical tweezing electrophoresis (OTE) apparatus was used. At deionised conditions μ=2.5 × 10−8 m2V−1s−1, it decreases further upon increasing the salt concentration c. Measurements at larger Φ generally show much larger μ and a qualitatively different dependence on c. At no added salt μ increases in the unordered state but a saturation at μ=6.8 × 10−8 m2V−1s−1 is observed, as the system develops fluid order. The fluid-crystal phase transition is…

PhysicsMean squared displacementElectrokinetic phenomenaPhase transitionRange (particle radiation)ElectrophoresisAnalytical chemistrySPHERESConductivitySaturation (chemistry)
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Influence of carboxylic acids on the stereospecific nicotinamide adenine dinucleotide-dependent and nicotinamide adenine dinucleotide-independent lac…

1971

Leuconostoc mesenteroides increased its lactic acid production from glucose threefold when malic acid was added to the culture. This increase resulted also in a reduction of the ratio of d -lactic acid to l -lactic acid (31.5 to 1.23). Addition of malic acid increased 6.5-fold the specific activity of nicotinamide adenine dinucleotide (NAD)-linked l -lactate dehydrogenase and increased 3.2-fold that of NAD-linked d -lactate dehydrogenase. The Michaelis constant ( K m ) for NAD of the NAD-linked l -lactate dehydrogenase increased with the addition of malate, but no change was observed in the K m values for the respective d -enzyme. The effect of carboxylic acids on the NAD-linked l -lactate…

Physiology and MetabolismCarboxylic AcidsMalatesDehydrogenaseNicotinamide adenine dinucleotideBiologyMicrobiologyMalate dehydrogenasechemistry.chemical_compoundMolecular BiologyCell-Free SystemL-Lactate DehydrogenaseStereoisomerismElectrophoresis DiscNADMolecular biologyStimulation ChemicalLactic acidCulture MediaCitric acid cycleGlucosechemistryBiochemistryLactatesNAD+ kinaseBranched-chain alpha-keto acid dehydrogenase complexOxoglutarate dehydrogenase complexAcidsLeuconostocJournal of bacteriology
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The response ofAsterochloris erici(Ahmadjian) Skaloud et Peksa to desiccation: a proteomic approach

2013

The study of desiccation tolerance of lichens, and of their chlorobionts in particular, has frequently focused on the anti- oxidant system that protects the cell against photo-oxidative stress during dehydration/rehydration cycles. In this study, we used proteomic and transcript analyses to assess the changes associated with desiccation in the isolated phycobiont Aste- rochloris erici. Algae were dried either slowly (5-6 h) or rapidly (<60 min), and rehydrated after 24 h in the desiccated state. To identify proteins that accumulated during the drying or rehydration processes, we employed two-dimensional (2D) difference gel electrophoresis (DIGE) coupled with individual protein identificatio…

PhysiologyDifference gel electrophoresisPlant ScienceChlorophytaBiologymedicine.diseaseProteomicsbiology.organism_classificationDesiccation toleranceBiochemistryProteomemedicineUltrastructureDehydrationDesiccationPlant, Cell &amp; Environment
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Temperature adaptation influences the aggregation state of hemocyanin from Astacus leptodactylus.

2000

When Astacus leptodactylus were kept at various temperatures for several weeks, different ratios between di-hexameric and hexameric hemocyanins were observed in their hemolymph. The higher the temperature the more hexamers were present. This long-term adaptation to different temperatures or/and to temperature-induced pH-shifts as observed in the hemolymph has different effects on the expression of subunit types building up hexamers and those which covalently link two hexamers within the di-hexamers. The oxygen binding behaviour of di-hexameric hemocyanins from cold and warm adapted animals do not show differences with respect to affinity, Bohr effect and cooperativity.

PhysiologyEcologymedicine.medical_treatmentProtein subunitTemperatureCooperativityHemocyaninBohr effectmacromolecular substancesBiologyHydrogen-Ion ConcentrationAstacus leptodactylusbiology.organism_classificationBiochemistryAdaptation PhysiologicalCrustaceaHemolymphHemocyaninsmedicineBiophysicsAnimalsElectrophoresis Polyacrylamide GelAdaptationMolecular BiologyOxygen bindingComparative biochemistry and physiology. Part A, Molecularintegrative physiology
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