Search results for "Protein purification"

showing 10 items of 32 documents

2014

As traditional detergents might destabilize or even denature membrane proteins, amphiphilic polymers have moved into the focus of membrane-protein research in recent years. Thus far, Amphipols are the best studied amphiphilic copolymers, having a hydrophilic backbone with short hydrophobic chains. However, since stabilizing as well as destabilizing effects of the Amphipol belt on the structure of membrane proteins have been described, we systematically analyze the impact of the most commonly used Amphipol A8-35 on the structure and stability of a well-defined transmembrane protein model, the glycophorin A transmembrane helix dimer. Amphipols are not able to directly extract proteins from th…

MultidisciplinarybiologyChemistryMicelleTransmembrane proteinTransmembrane domainchemistry.chemical_compoundMembraneMembrane proteinBiochemistryProtein purificationBiophysicsbiology.proteinGlycophorinSodium dodecyl sulfatePLOS ONE
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Optimised lyophilisation-based method for different biomolecule single-extractions from the same rat brain sample: Suitability for RNA and protein ex…

2019

Abstract Background Optimisation of tissue processing procedures in preclinical studies reduces the number of animals used and allows integrated multilevel study in the same sample. Multiple extraction of different biomolecules from the same sample has several limitations. New method Using brain samples from rats subjected to ischemic stroke, we combined lyophilisation of flash-frozen tissue, mechanical pulverisation and cryopreservation in a method to optimise tissue handling and preservation for independent RNA or protein single-extract methods, and subsequent RT-qPCR or Western blot analyses. Results Lyophilisation resulted in 70% tissue weight loss. RNA (OD260/280∼1.8) and protein yield…

Proteomics0301 basic medicineCryopreservationSpecimen Handlinglaw.invention03 medical and health sciences0302 clinical medicinelawReference genesProtein purificationAnimalsFlash freezingMessenger RNAChromatographyChemistryGeneral NeuroscienceBrainTissue ProcessingRNARatsStrokeFreeze Drying030104 developmental biologyRNARNA extraction030217 neurology & neurosurgeryJournal of Neuroscience Methods
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Sample Preparation for Mass-spectrometry-based Proteomics Analysis of Ocular Microvessels

2019

The use of isolated ocular blood vessels in vitro to decipher the pathophysiological state of the eye using advanced technological approaches has greatly expanded our understanding of certain diseases. Mass spectrometry (MS)-based proteomics has emerged as a powerful tool to unravel alterations in the molecular mechanisms and protein signaling pathways in the vascular beds in health and disease. However, sample preparation steps prior to MS analyses are crucial to obtain reproducible results and in-depth elucidation of the complex proteome. This is particularly important for preparation of ocular microvessels, where the amount of sample available for analyses is often limited and thus, pose…

Proteomics0301 basic medicineSwineGeneral Chemical EngineeringComputational biologyEyeProteomicsMass spectrometryMass SpectrometryGeneral Biochemistry Genetics and Molecular Biology03 medical and health sciences0302 clinical medicineProtein purificationAnimalsHumansSample preparationGel electrophoresisMass spectrometry based proteomicsGeneral Immunology and MicrobiologyGeneral NeuroscienceAnalytic Sample Preparation Methods030104 developmental biologyMicrovesselsProteome030217 neurology & neurosurgeryChromatography LiquidHomogenization (biology)Journal of Visualized Experiments
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Proteomics evaluation of enniatins acute toxicity in rat liver

2021

Abstract Enniatins (ENs) are emerging mycotoxins produced by Fusarium fungi which are cytotoxic also at low concentrations due to its ionophoric properties. The aim of this study was to evaluate the hepatic toxicity of ENs exposure at different concentrations in Wistar rats through a proteomic approach. Animals were intoxicated by oral gavage with medium (EN A 256, ENA1 353, ENB 540, ENB1 296 μg/mL) and high concentrations (ENA 513, ENA1 706, ENB 1021, ENB1 593 μg/mL) of an ENs mixture and sacrificed after 8 h. Protein extraction was performed using powdered liver. Peptides were analyzed using a liquid chromatography coupled with a quadrupole time-of-flight mass spectrometer. Proteins were …

ProteomicsFusariumToxicologyProteomicsmedicine.disease_cause03 medical and health sciences0404 agricultural biotechnologyTandem Mass SpectrometryIn vivoDepsipeptidesIn vivoProtein purificationmedicineAnimalsRats Wistar030304 developmental biology0303 health sciencesbiologyChemistry04 agricultural and veterinary sciencesGeneral MedicineMetabolismMycotoxinsbiology.organism_classification040401 food scienceAcute toxicityRatsLiverBiochemistryOxidative stressElectron transport chainFemaleNAD+ kinaseBiomarkersOxidative stressChromatography LiquidFood ScienceFood and Chemical Toxicology
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Protein diffusion through charged nanopores with different radii at low ionic strength

2014

[EN] The diffusion of two similar molecular weight proteins, bovine serum albumin (BSA) and bovine haemoglobin (BHb), through nanoporous charged membranes with a wide range of pore radii is studied at low ionic strength. The effects of the solution pH and the membrane pore diameter on the pore permeability allow quantifying the electrostatic interaction between the chargedpore and the protein. Because of the large screening Debye length, both surface and bulk diffusion occur simultaneously. By increasing the pore diameter, the permeability tends to the bulk self-diffusion coefficient for each protein. By decreasing the pore diameter, the charges on the pore surface electrostatically hinder …

Self assembled monolayersUltrafiltration membranesSurface PropertiesPHStatic ElectricityAnalytical chemistryGeneral Physics and AstronomyDiffusionHemoglobinsNanoporessymbols.namesakeProtein purificationAnimalsHemoglobinParticle SizePhysical and Theoretical ChemistryBovine serum albuminMolecular transportAqueous solutionsSerum AlbuminDebye lengthChemical PhysicsbiologyNanoporousChemistryOsmolar ConcentrationMicroporous membranesLight scatteringSerum Albumin BovineBovineHydrogen-Ion ConcentrationSurfaceNanoporeMembraneIsoelectric pointBovine serum albuminPermeability (electromagnetism)Chemical physicsFISICA APLICADAPhysical SciencesChemical Sciencesbiology.proteinsymbolsCattlePorosity
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A study of the Candida albicans cell wall proteome

2008

Considering the importance of proteins in the structure and function of the cell wall of Candida albicans, we analyzed the cell wall subproteome of this important human pathogen by LC coupled to MS (LC-MS) using different protein extraction procedures. The analyzed samples included material extracted by hydrogen fluoride-pyridine (HF-pyridine), and whole SDS-extracted cell walls. The use of this latter innovative procedure gave similar data as compared to the analysis of HF-pyridine extracted proteins. A total of 21 cell wall proteins predicted to contain a signal peptide were identified, together with a high content of potentially glycosylated Ser/Thr residues, and the presence of a GPI mo…

Signal peptideProteomebiologyPyridinesSodium Dodecyl SulfateProteomicsbiology.organism_classificationBiochemistryHydrofluoric AcidCorpus albicansFungal ProteinsCell wallBiochemistryCell WallTandem Mass SpectrometryCandida albicansProteomeProtein purificationSolventsBlastosporeCandida albicansMolecular BiologyPROTEOMICS
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Superparamagnetic γ-Fe2O3 nanoparticles with tailored functionality for protein separation

2007

Polymer coated superparamagnetic gamma-Fe(2)O(3) nanoparticles were derivatized with a synthetic double-stranded RNA [poly(IC)], a known allosteric activator of the latent (2-5)A synthetase, to separate a single 35 kDa protein from a crude extract which cross reacted with antibodies raised against the sponge enzyme.

Surface PropertiesAllosteric regulationNanoparticleLigandsFerric CompoundsCatalysisMagneticsProtein purification2'5'-Oligoadenylate SynthetaseMaterials ChemistryAnimalsParticle Sizechemistry.chemical_classificationBinding SitesMolecular StructurebiologyImmunomagnetic SeparationMetals and AlloysRNADNA-Directed RNA PolymerasesGeneral ChemistryPolymerbiology.organism_classificationPoriferaSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSpongeEnzymeBiochemistrychemistryCeramics and CompositesNanoparticlesPeptidesSuperparamagnetismChemical Communications
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The main cold shock protein of Listeria monocytogenes belongs to the family of ferritin-like proteins

2000

The transfer of the food-borne pathogen Listeria monocytogenes from 30 to 5 degrees C was characterized by the sharp induction of a low molecular mass protein. This major cold shock protein has an isoelectric point at pH 5.1 and a molecular mass of about 18 kDa, as observed on two-dimensional gel electrophoresis (2-DE) pattern. Its N-terminal sequence, obtained from the 2-DE spot, shared a complete sequence identity with a Listeria innocua non-heme iron-binding ferritin. The purification of these ferritin-like proteins (Flp) revealed a native molecular mass of about 100-110 kDa which indicates a polypeptide composed of six 18 kDa-subunits. Northern analysis indicated the presence of a 0.8-k…

Transcription GeneticMolecular Sequence DataEFFET DE LA TEMPERATUREBiologyMicrobiologyBacterial ProteinsHeat shock proteinProtein purificationGeneticsHumansRNA MessengerMolecular Biology[SDV.MP] Life Sciences [q-bio]/Microbiology and ParasitologyComputingMilieux_MISCELLANEOUSGel electrophoresisMolecular massTemperatureCold-shock domainbiology.organism_classificationListeria monocytogenesMolecular biologyCold TemperatureFerritinRNA BacterialIsoelectric point[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyBiochemistryFerritinsbiology.proteinListeriaElectrophoresis Polyacrylamide GelHeat-Shock Response
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NovelAmycolatopsis balhimycinabiochemical abilities unveiled by proteomics

2014

Amycolatopsis balhimycina DSM5908 is an actinomycete producer of balhimycin, an analogue of vancomycin, the antibiotic of ‘last resort’ against multidrug-resistant Gram-positive pathogens. Most knowledge on glycopeptide biosynthetic pathways comes from studies on A. balhimycina as this strain, among glycopeptide producers, is genetically more amenable. The recent availability of its genome sequence allowed to perform differential proteomic analyses elucidating key metabolic pathways leading to antibiotic production in different growth conditions. To implement proteomic data on A. balhimycina derived from 2-DE approaches and to identify novel components, a combined approach based on protein …

Whole genome sequencingchemistry.chemical_classificationSpectrometry Mass Electrospray Ionizationmass spectrometry; 1D-electrophoresis; glycopeptide antibiotics; actinomycetes; glutamate dehydrogenaseProteomeBiologyProteomicsMicrobiologyGenomeActinomycetes proteomics 2D-DIGE Mass spectrometryGlycopeptideSynthetic biologyMetabolic pathwayEnzymeBiochemistrychemistryBacterial ProteinsTandem Mass SpectrometryProtein purificationActinomycetalesGeneticsElectrophoresis Polyacrylamide GelMolecular BiologyMetabolic Networks and Pathways
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Multifunctional polymer-derivatized γ-Fe2O3 nanocrystals as a methodology for the biomagnetic separation of recombinant His-tagged proteins

2008

Abstract Multifunctional polymer-derivatized superparamagnetic iron oxide (γ-Fe2O3) nanoparticles were prepared for biomagnetic separation of histidine-tagged recombinant proteins building up a faster and efficient method for protein separation by making use of their intrinsic magnetic properties. Using polymer bound γ-Fe2O3 nanocrystals, a 6× histidine-tagged recombinant protein (silicatein) with a molecular weight of 24 kDa has been isolated and purified. The supermagnetic iron oxide nanocrystals were characterized by transmission electron microscopy (TEM), high-resolution TEM (HRTEM), SQUID and Mossbauer and the polymer functionalization of the γ-Fe2O3 nanocrystals was monitored by UV–vi…

chemistry.chemical_classificationGel electrophoresisMaterials scienceIron oxideNanoparticlePolymerCondensed Matter PhysicsElectronic Optical and Magnetic Materialschemistry.chemical_compoundNuclear magnetic resonancechemistryChemical engineeringProtein purificationMicroscopyHigh-resolution transmission electron microscopySuperparamagnetismJournal of Magnetism and Magnetic Materials
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