Search results for "Spectrum analysis"

showing 10 items of 287 documents

New insight into the aptamer conformation and aptamer/protein interaction by surface-enhanced Raman scattering and multivariate statistical analysis

2021

International audience; We study the interaction between one aptamer and its analyte (the MnSOD protein) by the combination of surface-enhanced Raman scattering and multivariate statistical analysis. We observe the aptamer structure and its evolution during the interaction under different experimental conditions (in air or in buffer). Through the spectral treatment by principal component analysis of a large set of SERS data, we were able to probe the aptamer conformations and orientations relative to the surface assuming that the in-plane nucleoside modes are selectively enhanced. We demonstrate that the aptamer orientation and thus its flexibility rely strongly on the presence of a spacer …

Surface (mathematics)[PHYS]Physics [physics]AnalyteChemistryAptamer[SDV]Life Sciences [q-bio]02 engineering and technologyBiosensing TechniquesAptamers Nucleotide010402 general chemistry021001 nanoscience & nanotechnologySpectrum Analysis Raman01 natural sciences0104 chemical sciencessymbols.namesakesymbolsBiophysics[CHIM]Chemical SciencesGeneral Materials Science[NLIN]Nonlinear Sciences [physics]Multivariate statistical0210 nano-technologyRaman scattering
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Plasmonic nanostructures through DNA-assisted lithography

2018

DALI combines DNA origami with conventional top-down fabrication for creating designer high-resolution plasmonic nanostructures.

TechnologyMaterials scienceFabricationmaterials scienceta221ta220Nanotechnology02 engineering and technologySpectrum Analysis Raman010402 general chemistry01 natural sciencesplasmonicssymbols.namesakenanorakenteetnanostructuresDNA origamiDNA nanotechnologyComputer SimulationnanolithographyLithographyNanoscopic scaleResearch ArticlesPlasmonMultidisciplinaryta114PhysicsSciAdv r-articlesMetamaterialself-assemblyDNA021001 nanoscience & nanotechnologyoptics0104 chemical sciencesChemistryTemplateApplied Sciences and EngineeringsymbolsNucleic Acid ConformationPrintingDNA origami0210 nano-technologyRaman spectroscopyBiotechnologyResearch Article
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A study of electron transfer in Ru(dcbpy)2(NCS)2 sensitized nanocrystalline TiO2 and SnO2 films induced by red-wing excitation.

2008

Excited state dynamics and electron transfer from the Ru(dcbpy)2(NCS)2 (RuN3) sensitizer to semiconductor nanoparticles were studied using time-resolved femtosecond absorption spectroscopy. We found that excitation of the red wing of the absorption spectrum of the sensitizer populates the (3)MLCT state directly, both in solution and attached on semiconductor nanoparticle films. Electron injection is slowed down and becomes gradually less efficient as excitation moves towards red from the absorption maximum at 535 nm. At 675 nm the injection is non-exponential and characterized by 5, 30 and 180 ps time constants. The non-exponential electron injection observed is assigned to injection from a…

Time FactorsAbsorption spectroscopyPhotochemistrySurface PropertiesAnalytical chemistryGeneral Physics and AstronomyElectronsSensitivity and SpecificityRutheniumElectron transferOrganometallic CompoundsPhysical and Theoretical ChemistryTriplet stateAbsorption (electromagnetic radiation)Coloring AgentsTitaniumChemistrybusiness.industryLasersSpectrum AnalysisTin CompoundsMembranes ArtificialNanocrystalline materialNanostructuresKineticsSemiconductorSemiconductorsExcited stateFemtosecondbusinessThiocyanatesPhysical chemistry chemical physics : PCCP
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Ferricytochrome c encapsulated in silica hydrogels: correlation between active site dynamics and solvent structure.

2003

Ferricytochrome c encapsulated in silica hydrogels has been prepared by the sol-gel technique following, with some modifications, the procedure originally developed by Ellerby et al. (Science 255 1113 (1992)). A suitable preparation of hydrogels enables having both 'wet' and 'dry' samples. Wet samples have a high water content: as the temperature is lowered below approximately 260 K, water freezes and the samples crack. On the contrary, dry samples have a low water content (hydration h approximately equal 0.35): in these conditions water does not freeze even at cryogenic temperatures and the samples remain transparent and non-cracking. The dynamics of ferricytochrome c and its dependence on…

Time FactorsAbsorption spectroscopySilicon dioxideDrug CompoundingAnalytical chemistryBiophysicsSilica GelCapsulesCytochrome c GroupSpectrum Analysis RamanBiochemistrychemistry.chemical_compoundDrug StabilityFreezingAnimalsHorsesWater contentBinding SitesbiologySilica gelSpectrum AnalysisOrganic ChemistryTemperatureActive siteWaterHydrogelsAtmospheric temperature rangeSilicon DioxideSolventKineticschemistrySelf-healing hydrogelsbiology.proteinSolventsBiophysical chemistry
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Fluctuation Methods To Study Protein Aggregation in Live Cells: Concanavalin A Oligomers Formation

2011

Prefibrillar oligomers of proteins are suspected to be the primary pathogenic agents in several neurodegenerative diseases. A key approach for elucidating the pathogenic mechanisms is to probe the existence of oligomers directly in living cells. In this work, we were able to monitor the process of aggregation of Concanavalin A in live cells. We used number and brightness analysis, two-color cross number and brightness analysis, and Raster image correlation spectroscopy to obtain the number of molecules, aggregation state, and diffusion coefficient as a function of time and cell location. We observed that binding of Concanavalin A to the membrane and the formation of small aggregates paralle…

Time FactorsCell SurvivalCellSpectroscopy Imaging and Other TechniquesBiophysicsProtein aggregationCell morphologyCell membraneDiffusion03 medical and health scienceschemistry.chemical_compoundMice0302 clinical medicineProtein structure2-NaphthylaminemedicineConcanavalin AAnimalsconfocal microscopy super resolution protein aggregation kinetics in live cells amyloid related pathologiesAnnexin A5Protein Structure QuaternaryCell Shape030304 developmental biology0303 health sciencesbiologySpectrum AnalysisCell MembraneFibroblastsEmbryo MammalianCell biologyMembranemedicine.anatomical_structurechemistryConcanavalin Abiology.proteinLaurdan030217 neurology & neurosurgeryFluorescein-5-isothiocyanateLaurates
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Concurrent fast and slow synchronized efferent phrenic activities in time and frequency domain.

1990

Abstract In urethane-anesthetized or decerebrated vagotomized rabbits efferent multifiber activity of the phrenic nerve was investigated for synchronized activities both in time and frequency domains. When respiratory drive was steadily increased by either an elevation of end-tidal CO2 concentration or i.v. administration of 4-aminopyridine, medium-frequency oscillations (MFO) first increased, then decreased and finally became absent. The power of high-frequency oscillations (HFO) steadily rose with increasing respiratory drive. In contrast to HFO which revealed a unimodal spectral peak of mostly small bandwidth, the MFO spectrum in most cases consisted of a broad complex. This complex in s…

Time FactorsEfferentEfferent PathwaysNerve FibersCo2 concentrationmedicineRecording electrodeTidal VolumeAnimals4-AminopyridineMolecular BiologyBroad complexPhrenic nerveChemistryGeneral NeuroscienceRespirationSpectrum Analysis4-AminopyridineRats Inbred StrainsCarbon DioxideRatsPhrenic NerveControl of respirationFrequency domainBiophysicsNeurology (clinical)RabbitsDevelopmental Biologymedicine.drugBrain research
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Time-Gated Raman Spectroscopy for Quantitative Determination of Solid-State Forms of Fluorescent Pharmaceuticals

2018

Raman spectroscopy is widely used for quantitative pharmaceutical analysis, but a common obstacle to its use is sample fluorescence masking the Raman signal. Time-gating provides an instrument-based method for rejecting fluorescence through temporal resolution of the spectral signal and allows Raman spectra of fluorescent materials to be obtained. An additional practical advantage is that analysis is possible in ambient lighting. This study assesses the efficacy of time-gated Raman spectroscopy for the quantitative measurement of fluorescent pharmaceuticals. Time-gated Raman spectroscopy with a 128 X (2) X 4 CMOS SPAD detector was applied for quantitative analysis of ternary mixtures of sol…

Time Factorsspektroskopia116 Chemical sciencesAnalytical chemistry02 engineering and technologySpectrum Analysis Raman01 natural sciencesSignalAnalytical Chemistrysymbols.namesakeTime domainLeast-Squares Analysista116DETECTORFluorescent DyesSUPPRESSIONta113ta114Chemistry010401 analytical chemistryDetectorMIXTURESSENSORPIROXICAMRESONANCE021001 nanoscience & nanotechnologyRAY-POWDER DIFFRACTIONFluorescence0104 chemical sciencesSPADPharmaceutical PreparationsPHOTON AVALANCHE-DIODETemporal resolutionRaman spectroscopysymbolsCRYSTALLIZATION0210 nano-technologyRaman spectroscopyTernary operationQuantitative analysis (chemistry)
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Switch between tyrosinase and catecholoxidase activity of scorpion hemocyanin by allosteric effectors

2008

AbstractPhenoloxidases and hemocyanins have similar type 3 copper centers although they perform different functions. Hemocyanins are oxygen carriers, while phenoloxidases (tyrosinase/catecholoxidase) catalyze the initial step in melanin synthesis. Tyrosinases catalyze two subsequent reactions, whereas catecholoxidases catalyze only the second one. Recent results indicate that hemocyanins can also function as phenoloxidases and here we show for the first time that hemocyanin can be converted to phenoloxidase. Furthermore, its substrate specificity can be switched between catecholoxidase and tyrosinase activity depending on effectors such as hydroxymethyl-aminomethan (Tris) and Mg2+-ions. Thi…

TrisStereochemistrymedicine.medical_treatmentTyrosinaseDopamineAllosteric regulationActivated hemocyaninBiophysicsMagnesium ChlorideTyramineType 3 copper proteinchemical and pharmacologic phenomenaBiochemistryCatalysisSubstrate SpecificityScorpionschemistry.chemical_compoundEnzyme activatorAllosteric RegulationStructural BiologyHemolymphHemolymphGeneticsmedicineAnimalsCatechol oxidaseMolecular BiologyScorpion Pandinus imperatorbiologyMonophenol MonooxygenaseSpectrum AnalysisActive siteCatecholoxidaseHemocyaninCell BiologyEnzyme ActivationchemistryBiochemistryHemocyaninsbiology.proteinTyrosinaseCatechol OxidaseFEBS Letters
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Purification and spectroscopic studies on catechol oxidases from Lycopus europaeus and Populus nigra: evidence for a dinuclear copper center of type …

1999

We purified two catechol oxidases from Lycopus europaeus and Populus nigra which only catalyze the oxidation of catechols to quinones without hydroxylating tyrosine. The molecular mass of the Lycopus enzyme was determined to 39,800 Da and the mass of the Populus enzyme was determined to 56,050 Da. Both catechol oxidases are inhibited by thiourea, N-phenylthiourea, dithiocarbamate, and cyanide, but show different pH behavior using catechol as substrate. Atomic absorption spectrosopic analysis found 1.5 copper atoms per protein molecule. Using EPR spectroscopy we determined 1.8 Cu per molecule catechol oxidase. Furthermore, EPR spectroscopy demonstrated that catechol oxidase is a copper enzym…

TyrosinaseCatecholschemistry.chemical_elementPhotochemistrySpectrum Analysis RamanBiochemistrylaw.inventionTreesInorganic Chemistrychemistry.chemical_compoundlawPolymer chemistryEnzyme InhibitorsElectron paramagnetic resonanceCatechol oxidaseCatecholBinding SitesCyanidesbiologyMonophenol MonooxygenaseSpectrophotometry AtomicElectron Spin Resonance SpectroscopySubstrate (chemistry)Bridging ligandHydrogen-Ion ConcentrationPlantsPhenylthioureaCopperMolecular WeightchemistryHemocyaninsbiology.proteinSpectrophotometry UltravioletOxygen bindingCatechol OxidaseCopperJournal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry
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Amorphous calcium carbonate in the shells of adult Unionoida

2011

Shells of adult individuals from two different bivalve families, Hyriopsis cumingii and Diplodon chilensis patagonicus, were studied by Micro-Raman spectroscopy and Focussed Ion Beam-assisted TEM. The shells contain amorphous calcium carbonate in a zone at the interface between the periostracum and the prismatic layer. In this area, the initial prism structures protrude from the inner periostracum layer and it is demonstrated that these structures systematically consist of highly disordered and amorphous calcium carbonate. Within this zone, ordered and disordered areas are intermingled discounting the existence of a crystallization front and favouring models of domainal crystallization proc…

UnionoidabiologyPeriostracumMineralogy550 - Earth sciencesbiology.organism_classificationSpectrum Analysis RamanPrism (geology)Amorphous calcium carbonatelaw.inventionAmorphous solidBivalviaCalcium Carbonatechemistry.chemical_compoundChemical engineeringchemistryMicroscopy Electron TransmissionStructural BiologylawPhase (matter)VateriteAnimalsCrystallization
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