Search results for "Affinity"

showing 10 items of 313 documents

Preparation of hepatitis C virus structural and non-structural protein fragments and studies of their immunogenicity

2006

Abstract Plasmids pQE-60 and pQE-30 containing 6× His-tag sequence were used for expression of fragments of HCV structural and non-structural proteins in Escherichia coli (E. coli). The following fragments were used: core (1–98 aa), NS3 (202–482 aa), and tetramer of hypervariable region 1 (HVR1) of E2 protein. The constructed plasmids directed high levels of expression of HCV proteins in E. coli JM109. After purification by the metal-affinity chromatography on nickel–nitrilotriacetic acid (Ni–NTA) agarose, the His-tagged HCV proteins were used for immunization of BALB/c mice. All three proteins were able to induce high levels of specific antibodies and, in the case of the NS3 and HVR1 tetra…

Nitrilotriacetic AcidHepatitis C virusDose-Response Relationship ImmunologicViral Nonstructural ProteinsBiologymedicine.disease_causeSensitivity and SpecificityChromatography AffinityAntigen-Antibody ReactionsMiceViral Proteinschemistry.chemical_compoundPlasmidTetramerNickelmedicineAnimalsCloning MolecularEscherichia coliCell ProliferationMice Inbred BALB CNS3Viral Core ProteinsImmunogenicityvirus diseasesHepatitis C AntibodiesVirologyMolecular biologyPeptide FragmentsRecombinant Proteinsdigestive system diseasesHypervariable regionchemistryAgaroseFemaleImmunizationHepatitis C AntigensPeptidesSpleenBiotechnologyProtein Expression and Purification
researchProduct

Laser photodetachment of radioactive $^{128}$I$^−$

2017

International audience; The first experimental investigation of the electron affinity (EA) of a radioactive isotope has been conducted at the CERN-ISOLDE radioactive ion beam facility. The EA of the radioactive iodine isotope (128)I (t (1/2) = 25 min) was determined to be 3.059 052(38) eV. The experiment was conducted using the newly developed Gothenburg ANion Detector for Affinity measurements by Laser PHotodetachment (GANDALPH) apparatus, connected to a CERN-ISOLDE experimental beamline. (128)I was produced in fission induced by 1.4 GeV protons striking a thorium/tantalum foil target and then extracted as singly charged negative ions at a beam energy of 20 keV. Laser photodetachment of th…

Nuclear and High Energy PhysicsIon beamFissionPhysics::Instrumentation and Detectors[PHYS.PHYS.PHYS-ACC-PH]Physics [physics]/Physics [physics]/Accelerator Physics [physics.acc-ph]02 engineering and technologyPhoton energy01 natural sciences7. Clean energySecondary electronsISOLDElaw.inventionIonlawElectron affinity0103 physical scienceselectron affinityPhysics::Atomic Physics010306 general physicsNuclear ExperimentPhysicsiodinephotodetachment021001 nanoscience & nanotechnologyLaserAccelerators and Storage RingsBeamlinePhysics::Accelerator PhysicsAtomic physics0210 nano-technology
researchProduct

Photoaffinity cross-linking of F1ATPase from spinach chloroplasts by 3'-arylazido-beta-alanyl-8-azido ATP.

1994

UV irradiation of the ATPase (CF1) from spinach chloroplasts in the presence of 3'-arylazido-beta-alanyl-8-azido ATP (8,3'-DiN3ATP) results in a nucleotide-dependent inactivation of the enzyme and in a nucleotide-dependent formation of alpha-beta cross-links. The results demonstrate an interfacial localization of the nucleotide binding sites on CF1.

Nucleotide binding siteAzidesChloroplastsStereochemistryPhotochemistryAffinity labelATPaseBiophysicsBiochemistryChloroplastF1ATPasechemistry.chemical_compoundAdenosine TriphosphateStructural BiologyVegetablesGeneticsBinding siteChenopodiaceaeInterfacial localizationMolecular BiologyPhotoaffinity cross-linkingchemistry.chemical_classificationbiologyfood and beveragesAffinity LabelsCell Biologybiology.organism_classificationChloroplastProton-Translocating ATPasesEnzymeCross-Linking Reagentschemistrybiology.proteinSpinach chloroplastAdenosine triphosphateFEBS letters
researchProduct

Natural co-occurrence of ochratoxin A, ochratoxin B and aflatoxins in Sicilian red wines

2015

The natural occurrence of ochratoxin A, ochratoxin B, aflatoxin B1, aflatoxin B2, aflatoxin G1 and aflatoxin G2 (OTA, OTB, AFB1, AFB2, AFG1, AFG2) in red wines was investigated by HPLC/FLD after immunoaffinity column clean-up in 57 market samples produced in Sicily (Italy). The results showed a very low incidence of these mycotoxins in analysed samples, confirming the high degree of quality and safety of Sicilian red wines. The results indicated 71.9% and 64.9% positive samples for OTA and OTB respectively, with an average level of 0.13 μg l(-1), well below the European maximum permitted levels (MLs). The aflatoxin most frequently detected in the samples was AFG1, present in 57.9% of sample…

Ochratoxin AAflatoxinAflatoxin B1Health Toxicology and MutagenesisOchratoxin BFood ContaminationWineAverage levelaflatoxin G2Toxicologyaflatoxin G1Sensitivity and SpecificityFluorescencechemistry.chemical_compoundAflatoxinsimmunoaffinity columnFood scienceHPLC/FLD analysiMycotoxinSicilyChromatography High Pressure LiquidWineChromatographyPublic Health Environmental and Occupational HealthGeneral ChemistryGeneral MedicineOchratoxinsimmunoaffinity column wine aflatoxin B-2 aflatoxin G(1) ochratoxin B ochratoxin A aflatoxin B-1 aflatoxin G(2) HPLC/FLD analysischemistryaflatoxin B2Maximum Allowable Concentrationochratoxin Aochratoxin BFood Science
researchProduct

Theoretical determination of the geometric and electronic structures of oligorylenes and poli(peri‐naphthalene)

1992

We present a theoretical investigation of the electronic structure of oligorylenes (from perylene to heptarylene, including also the naphthalene molecule) and their corresponding polymer poly(peri‐naphthalene) (PPN) using the nonempirical valence effective (VEH) method. The geometry of the unit cell used to generate the polymer is extrapolated from the PM3‐optimized molecular geometries of the longest oligorylenes. That geometry shows some bond alternation along the perimeter carbon chains and a bond length of ≊1.46 Å is calculated for the peri bonds connecting the naphthalene units. The VEH one‐electron energy level distributions calculated for oligorylenes are used to interpret the experi…

OptimizationChemical BondsBand gapStereochemistryExtrapolationElectric ConductorsGeometryGeneral Physics and AstronomyElectronic structureMolecular physicsEnergy LevelsMolecular orbitalPhysical and Theoretical ChemistryBand Structure:FÍSICA::Química física [UNESCO]Electronic band structurePeryleneFilmsValence (chemistry)Organic PolymersChemistryElectronic Structure ; Perylene ; Naphthalene ; Organic Polymers ; Unit Cell ; Geometry ; Extrapolation ; Optimization ; Chemical Bonds ; Carbon ; Chains ; Energy Levels ; Ionization Potential ; Affinity ; Band Structure ; Electric Conductors ; Films ; PyrolysisUnit CellChainsCarbonUNESCO::FÍSICA::Química físicaBond lengthIonization PotentialMolecular geometryElectronic StructureAffinityIonization energyNaphthalenePyrolysis
researchProduct

Theoretical study of the effect of substituent and backbone conformation on the electronic properties of symmetrically substituted poly(di‐n‐alkylsil…

1994

We present the results of ab initio 3‐21G∗ geometry optimizations and valence effective Hamiltonian (VEH) band structure calculations aimed at determining the evolution of the geometric and electronic (ionization potential, electron affinities, and band gaps) properties of all‐trans poly(dimethylsilane), poly(diethylsilane), poly(di‐n‐propylsilane), and poly(di‐n‐butylsilane) when increasing the size of the alkyl group. In the latter polymer, we have also studied the 7/3 conformation, in order to analyze the effect of the backbone conformation on the geometric and electronic structure. The VEH ionization potentials of all‐trans poly(di‐n‐alkylsilanes) are almost equal, and as experimental p…

OptimizationEnergy GapPropyl CompoundsBand gapAb initioSubstituentGeometryGeneral Physics and AstronomyElectronic structurechemistry.chemical_compoundAb initio quantum chemistry methodsComputational chemistryMethyl CompoundsConformational ChangesPhysical and Theoretical ChemistryBand Structure:FÍSICA::Química física [UNESCO]Electronic band structureAlkyl Compounds ; Silanes ; Organic Polymers ; Conformational Changes ; Ab Initio Calculations ; Geometry ; Optimization ; Band Structure ; Affinity ; Ionization Potential ; Energy Gap ; Methyl Compounds ; Ethyl Compounds ; Propyl CompoundsDimethylsilaneOrganic PolymersSilanesUNESCO::FÍSICA::Química físicaCrystallographyAlkyl CompoundsIonization PotentialAffinitychemistryEthyl CompoundsIonization energyAb Initio Calculations
researchProduct

A Newly-Detected Reductase fromRauvolfiaCloses a Gap in the Biosynthesis of the Antiarrhythmic Alkaloid Ajmaline

2002

A new enzyme, 1,2-dihydrovomilenine reductase (E.C. 1.3.1), has been detected in Rauvolfia cell suspension cultures. The enzyme specifically converts 2beta( R)-1,2-dihydrovomilenine through an NADPH-dependent reaction into 17-O-acetylnorajmaline, a close biosynthetic precursor of the antiarrhythmic alkaloid ajmaline from Rauvolfia. A five-step purification procedure using SOURCE 30Q chromatography, hydroxyapatite chromatography, 2',5'-ADP Sepharose 4B affinity chromatography and ion exchange chromatography on DEAE Sepharose and Mono Q delivered an approximately 200-fold enriched enzyme in a yield of approximately 6%. SDS-PAGE showed an M r for the enzyme of approximately 48 kDa. Optimum pH …

Oxidoreductases Acting on CH-CH Group DonorsRauvolfiaIon chromatographyPharmaceutical ScienceReductaseRauwolfiaAnalytical ChemistrySepharosechemistry.chemical_compoundAffinity chromatographyDrug DiscoverymedicineHumansChromatography High Pressure LiquidPharmacologychemistry.chemical_classificationAjmalinebiologyOrganic Chemistrybiology.organism_classificationAjmalineEnzymeComplementary and alternative medicinechemistryDEAE-SepharoseBiochemistryMolecular MedicineElectrophoresis Polyacrylamide GelOxidoreductasesAnti-Arrhythmia AgentsPhytotherapymedicine.drugPlanta Medica
researchProduct

A sensitive monoclonal antibody-based enzyme-linked immunosorbent assay to quantify Parietaria judaica major allergens, Par j 1 and Par j 2

2006

Summary Background Parietaria pollen is one of the most important causes of pollinosis in Mediterranean countries. Parietaria judaica pollen extract presents two major allergens, Par j 1 and Par j 2, that belong to the lipid transfer protein family. Objective To develop an ELISA for quantification of both major allergens of P. judaica pollen extracts, and to assert correlation of these allergens content with the allergenic activity of extracts. Methods Natural Par j 1–Par j 2 allergens were purified by gel filtration, ion exchange, and affinity chromatography and identified by mass spectrometry. Rabbit antisera were obtained using this protein preparation as antigen and used for immunoaffin…

Parietariamedicine.drug_classImmunologyEnzyme-Linked Immunosorbent Assaymedicine.disease_causeMonoclonal antibodySensitivity and SpecificityMiceAllergenAffinity chromatographyAntibody SpecificityHypersensitivityotorhinolaryngologic diseasesmedicineAnimalsHumansImmunology and AllergyPlant ProteinsAntiserumMice Inbred BALB Cbiologymedicine.diagnostic_testChemistryAntibodies MonoclonalAllergensbiology.organism_classificationMolecular biologyParietariaPolyclonal antibodiesImmunoassayImmunologyParietaria judaicabiology.proteinPollenClinical <html_ent glyph="@amp;" ascii="&"/> Experimental Allergy
researchProduct

Bloodstains on Leather: Examination of False Negatives in Presumptive Test and Human Hemoglobin Test.

2017

Presumptive tests for blood are very simple and sensitive tests used in the search for evidence. They also provide initial information on the nature of stains. A second test can confirm their nature. However, these tests can present false–negative results for different reasons. Some of those reasons have been studied, while others, those caused by the substrate material that contains the stain, are less well known. This work studies the effect of one component of a leather substrate—quebracho extract—on presumptive and human hemoglobin blood tests. Assays were performed using samples of blood dilutions contaminated with quebracho extract and others formed on a substrate containing the conta…

Pathologymedicine.medical_specialtyChromatographybusiness.industry010401 analytical chemistryForensic Sciences01 natural sciencesStainChromatography Affinity0104 chemical sciencesPathology and Forensic Medicine03 medical and health sciencesHemoglobins0302 clinical medicineBlood StainsGeneticsmedicineHumansFalse Positive ReactionsIndicators and Reagents030216 legal & forensic medicineHemoglobinbusinessTanninsBlood Chemical AnalysisJournal of forensic sciences
researchProduct

Immunoreactivity of monoclonal anti-melanoma antibodies in relation to the amount of radioactive iodine substituted to the antibody molecule.

1985

The damage to monoclonal anti-melanoma antibodies caused by iodination was investigated by comparing the results obtained using the chloramine-T method and the 1,3,4,6-tetrachloro-3 alpha, 6 alpha-diphenyl-glycoluril (IODOGEN) method at different levels of iodine substitution to the molecule. The level of substitution at which losses in immunoreactivity occurred was evaluated in each monoclonal antibody (MAb) studied. This phenomenon was not dependent on the method of substitution, provided that mild conditions of reaction were used. Lineweaver-Burk plots and--in cases of alterations in binding affinity--Scatchard plots were found to provide an adequate description of the binding behaviour …

Pathologymedicine.medical_specialtymedicine.drug_classAntibody Affinitychemistry.chemical_elementMice NudeMonoclonal antibodyIodineIodine RadioisotopesMiceIn vivoLabellingmedicineAnimalsHumansRadiology Nuclear Medicine and imagingBinding siteRadionuclide ImagingMelanomabiologyChemistryMelanomaAntibodies MonoclonalGeneral Medicinemedicine.diseaseMolecular biologyIsotope LabelingMonoclonalbiology.proteinBinding Sites AntibodyAntibodyEuropean journal of nuclear medicine
researchProduct