Search results for "bleaching"

showing 10 items of 107 documents

Effect of ATP Binding and Hydrolysis on Dynamics of Canine Parvovirus NS1▿ †

2010

ABSTRACT The replication protein NS1 is essential for genome replication and protein production in parvoviral infection. Many of its functions, including recognition and site-specific nicking of the viral genome, helicase activity, and transactivation of the viral capsid promoter, are dependent on ATP. An ATP-binding pocket resides in the middle of the modular NS1 protein in a superfamily 3 helicase domain. Here we have identified key ATP-binding amino acid residues in canine parvovirus (CPV) NS1 protein and mutated amino acids from the conserved A motif (K406), B motif (E444 and E445), and positively charged region (R508 and R510). All mutations prevented the formation of infectious viruse…

Models MolecularParvovirus CaninevirusesImmunologyMolecular Sequence DataPlasma protein bindingViral Nonstructural ProteinsMicrobiologyCell Linechemistry.chemical_compoundAdenosine TriphosphateDogsVirologyAnimalsAmino Acid SequenceBinding siteBinding SitesbiologyHydrolysisDNA replicationHelicaseFluorescence recovery after photobleachingFusion proteinMolecular biologyGenome Replication and Regulation of Viral Gene ExpressionProtein Structure TertiaryViral replicationchemistryBiochemistryAmino Acid SubstitutionInsect Sciencebiology.proteinCatsMutagenesis Site-DirectedSequence AlignmentDNAProtein Binding
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Effects of elevated hydrogen peroxide 'strip' bleaching on surface and subsurface enamel including subsurface histomorphology, micro-chemical composi…

2007

Abstract Objectives This study examined the effects of elevated concentration hydrogen peroxide tooth whitening treatments on tooth surface and subsurface integrity. Methods Sound human molars were ground and polished to prepare an uniform substrate for bleaching treatments. A cycling treatment included alternating ex vivo human salivary exposures with bleaching treatments under conditions of controlled temperature and durations of treatment. Bleaching was carried out with prototype bleaching strips containing hydrogen peroxide gel at 13% and 16% concentrations. A non-bleached group was used as a control. Treatments included 28 h of total bleaching exposure in vitro . Surface color was meas…

MolarToothbrushingMaterials scienceTime Factorsgenetic structuresBleachDentistryColorSpectrum Analysis RamanPeroxideFluorescencechemistry.chemical_compoundstomatognathic systemHardnessMaterials TestingDentinmedicineTooth BleachingHumansHydrogen peroxideDental EnamelSalivaGeneral DentistryDentifricesTooth whiteningMicroscopy ConfocalEnamel paintbusiness.industryTemperatureTooth surfaceHydrogen PeroxideOxidantsstomatognathic diseasesmedicine.anatomical_structurechemistryvisual_artDentinvisual_art.visual_art_mediumMicroscopy Electron ScanningColorimetrysense organsbusinessNuclear chemistryJournal of dentistry
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Effect of Hydrogen and Carbamide Peroxide in Bleaching, Enamel Morphology, and Mineral Composition: In vitro Study

2017

ABSTRACT Aim The aim of the study was to evaluate the bleaching effect, morphological changes, and variations in calcium (Ca) and phosphate (P) in the enamel with hydrogen peroxide (HP) and carbamide peroxide (CP) after the use of different application regimens. Materials and methods Four groups of five teeth were randomly assigned, according to the treatment protocol: HP 37.5% applied for 30 or 60 minutes (HP30, HP60), CP 16% applied for 14 or 28 hours (CP14, CP28). Changes in dental color were evaluated, according to the following formula: ΔE = [(La−Lb)2+(aa−ab)2 + (ba−bb)2]½. Enamel morphology and Ca and P compositions were evaluated by confocal laser scanning microscope and environmenta…

Morphology (linguistics)HydrogenDentistrychemistry.chemical_elementCarbamide Peroxide02 engineering and technologyIn Vitro TechniquesCalciumRandom Allocation03 medical and health scienceschemistry.chemical_compound0302 clinical medicineTooth BleachingHumansUreaDental EnamelTooth Bleaching AgentsHydrogen peroxideGeneral DentistryEnvironmental scanning electron microscopeTooth whiteningMineralsEnamel paintbusiness.industryHydrogen Peroxide030206 dentistry021001 nanoscience & nanotechnologyPhosphatePeroxideschemistryvisual_artvisual_art.visual_art_mediumTooth Discoloration0210 nano-technologybusinessToothNuclear chemistryThe Journal of Contemporary Dental Practice
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Effect of calcium hydroxide dressing on microleakage of composite restorations in endodontically treated teeth subsequent to bleaching

2009

Objective: This study evaluates the effect of calcium hydroxide dressing on microleakage of composite restorations following non-vital bleaching. Methods: A total of 45 sound extracted human maxillary central incisors underwent endodontic treatment. The teeth were randomly divided into three groups (n=15). In group 1, access cavities were restored with composite. In group 2, the teeth underwent a bleaching procedure for one week before being restored with composite. In group 3, following a bleaching procedure, calcium hydroxide paste was placed in the pulp chamber for one week. The teeth were then restored with composite. The specimens were subjected to a dye leakage test. The data was anal…

OrthodonticsDental LeakageTooth NonvitalCalcium hydroxideDye leakagebusiness.industryComposite numberDentistry:CIENCIAS MÉDICAS [UNESCO]BandagesCalcium Hydroxidechemistry.chemical_compoundOtorhinolaryngologychemistryUNESCO::CIENCIAS MÉDICASTooth BleachingHumansSurgeryMaxillary central incisorbusinessGeneral Dentistry
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Distribution and Dynamics of Transcription-Associated Proteins during Parvovirus Infection

2012

ABSTRACT Canine parvovirus (CPV) infection leads to reorganization of nuclear proteinaceous subcompartments. Our studies showed that virus infection causes a time-dependent increase in the amount of viral nonstructural protein NS1 mRNA. Fluorescence recovery after photobleaching showed that the recovery kinetics of nuclear transcription-associated proteins, TATA binding protein (TBP), transcription factor IIB (TFIIB), and poly(A) binding protein nuclear 1 (PABPN1) were different in infected and noninfected cells, pointing to virus-induced alterations in binding dynamics of these proteins.

Parvovirus CanineViral nonstructural proteinvirusesImmunologyMicrobiologyParvoviridae Infections03 medical and health sciencesVirologyAnimalsTranscription factor030304 developmental biology0303 health sciencesbiologyParvovirusBinding protein030302 biochemistry & molecular biologyCanine parvovirusFluorescence recovery after photobleachingbiology.organism_classificationMolecular biology3. Good healthVirus-Cell InteractionsCell CompartmentationInsect Sciencebiology.proteinTATA-binding proteinTranscription factor II BSubcellular FractionsTranscription Factors
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Parvovirus induced alterations in nuclear architecture and dynamics.

2009

The nucleus of interphase eukaryotic cell is a highly compartmentalized structure containing the three-dimensional network of chromatin and numerous proteinaceous subcompartments. DNA viruses induce profound changes in the intranuclear structures of their host cells. We are applying a combination of confocal imaging including photobleaching microscopy and computational methods to analyze the modifications of nuclear architecture and dynamics in parvovirus infected cells. Upon canine parvovirus infection, expansion of the viral replication compartment is accompanied by chromatin marginalization to the vicinity of the nuclear membrane. Dextran microinjection and fluorescence recovery after ph…

Parvovirus CaninevirusesGreen Fluorescent Proteinslcsh:MedicineGenome ViralKidneyParvoviridae InfectionsParvovirus03 medical and health sciencesLääketieteen bioteknologia - Medical biotechnologymedicineAnimalsHumansNuclear membraneMolecular Biology/Chromatin Structurelcsh:Science030304 developmental biologyMolecular Biology/DNA ReplicationCell Nucleus0303 health sciencesMultidisciplinaryMicroscopy ConfocalbiologyParvoviruslcsh:R030302 biochemistry & molecular biologyDNA replicationFluorescence recovery after photobleachingDextransbiology.organism_classificationMolecular biologyChromatin3. Good healthChromatinCell biologyCell nucleusmedicine.anatomical_structureViral replicationVirology/Viral Replication and Gene RegulationCatslcsh:QCell Biology/Nuclear Structure and FunctionViral genome replicationFluorescence Recovery After PhotobleachingHeLa CellsResearch ArticlePloS one
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Demonstration of Single-Barium-Ion Sensitivity for Neutrinoless Double-Beta Decay Using Single-Molecule Fluorescence Imaging

2018

[EN] A new method to tag the barium daughter in the double-beta decay of Xe-136 is reported. Using the technique of single molecule fluorescent imaging (SMFI), individual barium dication (Ba++) resolution at a transparent scanning surface is demonstrated. A single-step photobleach confirms the single ion interpretation. Individual ions are localized with superresolution (similar to 2 nm), and detected with a statistical significance of 12.9 sigma over backgrounds. This lays the foundation for a new and potentially background-free neutrinoless double-beta decay technology, based on SMFI coupled to high pressure xenon gas time projection chambers.

Physics - Instrumentation and DetectorsMaterials scienceMassesFOS: Physical sciencesGeneral Physics and Astronomychemistry.chemical_element01 natural sciences7. Clean energyMolecular physicsHigh Energy Physics - ExperimentIonTECNOLOGIA ELECTRONICAHigh Energy Physics - Experiment (hep-ex)Nuclear magnetic resonanceXenonDouble beta decay0103 physical sciencesNuclear Experiment (nucl-ex)010306 general physicsNuclear Experiment010308 nuclear & particles physicsBariumInstrumentation and Detectors (physics.ins-det)Single-molecule experimentPhotobleachingFluorescenceDicationchemistry
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Control of the electronic energy transfer pathway between two single fluorophores by dual pulse excitation.

2009

We report on the control of the energy transfer pathway in individual donor-acceptor dyads by proper timing of light pulses matching the donor and acceptor transition frequencies, respectively. Excitation of both chromophores at virtually the same time induces efficient singlet-singlet annihilation, whereby excitation energy effectively flows from the acceptor to the donor. The dual pulse excitation scheme implemented here allows for all-optical switching of the fluorescence intensity at the single-molecule level. The population of higher excited states at the donor site was found to significantly increase the photobleaching probability.

Physics::Biological Physicseducation.field_of_studyMaterials sciencePopulationGeneral Physics and AstronomyP680ChromophorePhotobleachingAcceptorCondensed Matter::Materials ScienceFörster resonance energy transferExcited statePhysics::Chemical PhysicsAtomic physicseducationExcitationPhysical review letters
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Modification of Plasma Membrane Organization in Tobacco Cells Elicited by Cryptogein

2014

Abstract Lipid mixtures within artificial membranes undergo a separation into liquid-disordered and liquid-ordered phases. However, the existence of this segregation into microscopic liquid-ordered phases has been difficult to prove in living cells, and the precise organization of the plasma membrane into such phases has not been elucidated in plant cells. We developed a multispectral confocal microscopy approach to generate ratiometric images of the plasma membrane surface of Bright Yellow 2 tobacco (Nicotiana tabacum) suspension cells labeled with an environment sensitive fluorescent probe. This allowed the in vivo characterization of the global level of order of this membrane, by which w…

Physiology[SDV]Life Sciences [q-bio]BiophysicsContext (language use)Pyridinium CompoundsPlant ScienceBiologyArticleFungal ProteinsTobaccoGeneticsMembrane fluidity[SDV.BV]Life Sciences [q-bio]/Vegetal BiologyFluorescent DyesPlasma membrane organizationChromatographyMicroscopy ConfocalPhotobleachingCell MembraneFluorescence recovery after photobleachingMembrane raftfood and beveragesPlant cellElicitorSterolsMembrane[SDE]Environmental SciencesBiophysicsFlagellinSignal Transduction
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Functional size of complement and perforin pores compared by confocal laser scanning microscopy and fluorescence microphotolysis

1991

Abstract Confocal laser scanning microscopy and fluorescence microphotolysis (also referred to as fluorescence photobleaching recovery) were employed to study the transport of hydrophilic fluorescent tracers through complement and perforin pores. By optimizing the confocal effect it was possible to determine the exclusion limit of the pores in situ, i.e. without separation of cells and tracer solution. Single-cell flux measurements by fluorescence microphotolysis yielded information on the sample population distribution of flux rates. By these means a direct comparison of complement and perforin pores was made in sheep erythrocyte membranes. In accordance with previous studies employing a v…

Pore Forming Cytotoxic ProteinsIn situCell Membrane PermeabilityConfocalBiophysicsAntigen-Antibody ComplexIn Vitro TechniquesBiologyBiochemistryTumor Cells CulturedmedicineAnimalsHumansMembrane GlycoproteinsSheepPerforinLasersCell MembraneErythrocyte MembraneMembrane ProteinsComplement System ProteinsCell BiologyFluorescencePhotobleachingCell biologyRed blood cellmedicine.anatomical_structureMembranePerforinMicroscopy Electron Scanningbiology.proteinCytolysinBiochimica et Biophysica Acta (BBA) - Biomembranes
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