Search results for "Specificity."

showing 10 items of 2232 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
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Emergence and Phylodynamics of Citrus tristeza virus in Sicily, Italy

2013

Citrus tristeza virus (CTV) outbreaks were detected in Sicily island, Italy for the first time in 2002. To gain insight into the evolutionary forces driving the emergence and phylogeography of these CTV populations, we determined and analyzed the nucleotide sequences of the p20 gene from 108 CTV isolates collected from 2002 to 2009. Bayesian phylogenetic analysis revealed that mild and severe CTV isolates belonging to five different clades (lineages) were introduced in Sicily in 2002. Phylogeographic analysis showed that four lineages co-circulated in the main citrus growing area located in Eastern Sicily. However, only one lineage (composed of mild isolates) spread to distant areas of Sici…

Nonsynonymous substitutionCitrusGenetic-variationLineage (evolution)Population Dynamicslcsh:MedicinePopulation geneticsPlant Sciencelcsh:SciencePhylogenetic analysesPhylogenyGeneticsMultidisciplinarybiologyPhylogenetic treeGeographyCitrus tristeza virusAgriculturePhylogeneticsItalyRNA ViralEvolutionary dynamicsCross-protectionSequence AnalysisResearch ArticleClosterovirusDNA ComplementaryMolecular Sequence DataPlant PathogensCropsMicrobiologyViral EvolutionFruitsGenetic driftSpecies SpecificityVirologyMosaic-virusGenetic variationCTV Phylodynamics SicilyEvolutionary SystematicsPopulation-structureHost passageBiologyPlant DiseasesEvolutionary BiologyMaximum-likelihoodlcsh:RSettore AGR/12 - Patologia VegetaleComputational BiologyGenetic VariationBayes TheoremSequence Analysis DNAPlant Pathologybiology.organism_classificationAgronomyViral phylodynamicsDNA polymorphismEvolutionary biologyMolecular evolutionlcsh:Q
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NATURAL SELECTION AND THE ORGAN-SPECIFIC DIFFERENTIATION OF HIV-1 V3 HYPERVARIABLE REGION

2004

The existence of organ-specific HIV-1 populations within infected hosts has been studied for many years; nonetheless results reported by different authors are somewhat discrepant. To tackle this problem, we used a population genetics approach to analyze previously published data from the V3 hypervariable region of the envelope env gene. Our results are compatible with a population subdivision by organs in 95% of individuals analyzed at autopsy. In addition, populations infecting the nervous system and testicles clearly appear as differentiated subsets of the so-called macrophage-tropic variants. Liver and kidney may harbor differentiated populations as well. Although it is widely accepted t…

Nonsynonymous substitutionPopulationPopulation geneticsHIV Envelope Protein gp120BiologyEvolution MolecularGeneticsCluster AnalysisHumansSelection GeneticeducationEcology Evolution Behavior and SystematicsGeneticsAnalysis of VarianceLikelihood Functionseducation.field_of_studyNatural selectionBase SequenceModels GeneticMechanism (biology)HIVPeptide FragmentsHypervariable regionGenetics PopulationOrgan SpecificityViral evolutionAdaptationDatabases Nucleic AcidGeneral Agricultural and Biological SciencesSequence AlignmentEvolution
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Propagation pattern analysis during atrial fibrillation based on the adaptive group LASSO.

2012

The present study introduces sparse modeling for the estimation of propagation patterns in intracardiac atrial fibrillation (AF) signals. The estimation is based on the partial directed coherence (PDC) function, derived from fitting a multivariate autoregressive model to the observed signals. A sparse optimization method is proposed for estimation of the model parameters, namely, the adaptive group least absolute selection and shrinkage operator (aLASSO). In simulations aLASSO was found superior to the commonly used least-squares (LS) estimation with respect to estimation performance. The normalized error between the true and estimated model parameters dropped from 0.200.04 for LS estimatio…

Normalization (statistics)Computer scienceBiomedical EngineeringHealth InformaticsGroup lassoSensitivity and SpecificityPattern Recognition AutomatedHeart Conduction SystemStatisticsAtrial FibrillationCoherence (signal processing)AnimalsHumansComputer SimulationDiagnosis Computer-AssistedTime series1707ShrinkageSparse matrixPropagation patternModels CardiovascularReproducibility of ResultsElectroencephalographySignal ProcessingSettore ING-INF/06 - Bioingegneria Elettronica E InformaticaAlgorithmAlgorithmsAnnual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference
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Sensitivity enhancement in pulse EPR distance measurements

2004

Established pulse EPR approaches to the measurement of small dipole-dipole couplings between electron spins rely on constant-time echo experiments to separate relaxational contributions from dipolar time evolution. This requires a compromise between sensitivity and resolution to be made prior to the measurement, so that optimum data are only obtained if the magnitude of the dipole-dipole coupling is known beforehand to a good approximation. Moreover, the whole dipolar evolution function is measured with relatively low sensitivity. These problems are overcome by a variable-time experiment that achieves suppression of the relaxation contribution by reference deconvolution. Theoretical and exp…

Nuclear and High Energy PhysicsProtein ConformationBiophysicsAnalytical chemistryBiochemistrySensitivity and Specificitylaw.inventionlawspin labelingSensitivity (control systems)protein structurepair correlation functionElectron paramagnetic resonanceCouplingSpinsChemistryPulsed EPRRelaxation (NMR)Time evolutionElectron Spin Resonance SpectroscopyPhotosystem II Protein ComplexReproducibility of ResultsSignal Processing Computer-AssistedELDORCondensed Matter PhysicsComputational physicsDeconvolutionEPRAlgorithms
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Improvement of ESR dosimetry for thermal neutron beams through the addition of gadolinium.

2007

In this paper, the addition of gadolinium is proposed as a useful tool to enhance the electron spin resonance (ESR) sensitivity of organic compounds to thermal neutrons. The target of this work is the detection, through the ESR technique, of the thermal neutron fluence in a mixed field of photons and neutrons. Gadolinium was chosen because it has a very high capture cross section to thermal neutrons; its nuclear reaction with thermal neutrons induces complex inner shell transitions that generate, besides other particles, Auger electrons, which in turn release their energy in the neighborhood (only several nanometers) of the place of reaction. Gadolinium was added to two organic molecules: a…

Nuclear reactionMaterials scienceHot TemperaturePhysics::Instrumentation and DetectorsGadoliniumPhysics::Medical PhysicsAnalytical chemistrychemistry.chemical_elementGadoliniumRadiation DosageFluenceSensitivity and Specificitylaw.inventionsymbols.namesakeNuclear magnetic resonancelawRadiology Nuclear Medicine and imagingNeutronElectron paramagnetic resonanceRadiometryNeutronsDosimeterRadiological and Ultrasound TechnologyAuger effectElectron Spin Resonance SpectroscopyReproducibility of ResultsNeutron temperatureESR dosimetry thermal neutron gadoliniumchemistrysymbolsCondensed Matter::Strongly Correlated ElectronsPhysics in medicine and biology
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CHEMICAL AND PHYSICAL SIGNALS MEDIATING CONSPECIFIC AND HETEROSPECIFIC AGGREGATION BEHAVIOR OF FIRST INSTAR STINK BUGS

2004

We investigated cues that mediate the aggregation behavior of immature pentatomid bugs by using nymphs of six different pentatomid bug species (Nezara viridula, Acrosternum hilare, Chlorochroa ligata, Chlorochroa sayi, Thyanta pallidovirens, and Euschistus conspersus). When first instars of any two species were put together in a Petri dish, they readily formed heterospecific aggregations similar to their natural conspecific aggregations. The chemical profiles of first and second instar nymphs of each species were determined by solvent extraction with pentane, followed by GC-MS analysis. Immature bugs of the different species had some compounds in common, and some that were more species spec…

NymphTime Factorsanimal structuresEggsAllomoneInsect ControlBiochemistryGas Chromatography-Mass SpectrometryPheromoneslaw.inventionHeteropteraSexual Behavior AnimalSpecies SpecificitylawBotanyAnimalsNymphEcology Evolution Behavior and SystematicsDemographyDose-Response Relationship DrugbiologyPetri dishfungiGeneral MedicinePentatomidaebiology.organism_classificationEuschistus conspersusNezara viridulaInstarVolatilizationThyanta pallidovirens
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Identification of a lysyl residue defining the binding specificity of a human odorant-binding protein

2008

International audience

OBP[CHIM.OTHE] Chemical Sciences/OtherLYSYL RESIDUEBINDING SPECIFICITY[CHIM.OTHE]Chemical Sciences/OtherComputingMilieux_MISCELLANEOUSODORANT-BINDING PROTEIN
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Bermanella marisrubri gen. nov., sp. nov., a genome-sequenced gammaproteobacterium from the Red Sea

2009

5 pages, 2 figures, 1 table

OceanospirillaceaeThalassolituusMolecular Sequence DataZoologyBiologyMicrobiologyGenomeSpecies SpecificityBermanella marisrubriGenusRNA Ribosomal 16SGenotypeBotanyIndian OceanPhylogenyEcology Evolution Behavior and Systematicsvisual_art.artworkPhylogenetic treeGeneral Medicine16S ribosomal RNAbiology.organism_classificationPhenotypevisual_artWater MicrobiologyGenome BacterialBacteriaINTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY
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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
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