Search results for "Dyes"

showing 10 items of 324 documents

Toward oxygen binding curves of single respiratory proteins

2004

Oxygen binding curves of single molecules promise to discriminate between different models describing cooperativity because load distributions are accessible. Individual tarantula hemocyanins could be detected by fluorescence correlation spectroscopy using intrinsic tryptophan fluorescence as sensor of bound oxygen. However, imaging of immobilized proteins was not possible due to fast photo-bleaching. It is shown that tetra-methyl-carboxy-rhodamine (TAMRA), commonly used as a fluorescence label in single-molecule spectroscopy, can also be applied to monitor bound oxygen. The dye's fluorescence is quenched due to Förster energy transfer to the oxygenated active sites of hemocyanin.

Rhodaminesmedicine.medical_treatmentAnalytical chemistryGeneral Physics and Astronomychemistry.chemical_elementSpidersHemocyaninFluorescence correlation spectroscopyCooperativityCell BiologyFluorescenceOxygenOxygenchemistryStructural BiologyHemocyaninsmedicineBiophysicsAnimalsMoleculeGeneral Materials ScienceSpectroscopyOxygen bindingFluorescent DyesMicron
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Expanding the chemical scope of RNA:methyltransferases to site-specific alkynylation of RNA for click labeling.

2010

This work identifies the combination of enzymatic transfer and click labeling as an efficient method for the site-specific tagging of RNA molecules for biophysical studies. A double-activated analog of the ubiquitous co-substrate S-adenosyl-l-methionine was employed to enzymatically transfer a five carbon chain containing a terminal alkynyl moiety onto RNA. The tRNA:methyltransferase Trm1 transferred the extended alkynyl moiety to its natural target, the N2 of guanosine 26 in tRNA(Phe). LC/MS and LC/MS/MS techniques were used to detect and characterize the modified nucleoside as well as its cycloaddition product with a fluorescent azide. The latter resulted from a labeling reaction via Cu(I…

S-AdenosylmethioninetRNA MethyltransferasesBase SequenceStereochemistryMolecular Sequence DataGuanosineRNAFluorescence correlation spectroscopyBiologyTRNA Methyltransferaseschemistry.chemical_compoundRNA Transfer PheSpectrometry FluorescencechemistryBiochemistryAlkynesTransfer RNASynthetic Biology and ChemistryGeneticsClick chemistryMoietyClick ChemistryAzideOrganic ChemicalsFluorescent DyesNucleic acids research
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A synthetic biology approach for the fabrication of functional (fluorescent magnetic) bioorganic–inorganic hybrid materials in sponge primmorphs

2020

During evolution, sponges (Porifera) have honed the genetic toolbox and biosynthetic mechanisms for the fabrication of siliceous skeletal components (spicules). Spicules carry a protein scaffold embedded within biogenic silica (biosilica) and feature an amazing range of optical, structural, and mechanical properties. Thus, it is tempting to explore the low-energy synthetic pathways of spiculogenesis for the fabrication of innovative hybrid materials. In this synthetic biology approach, the uptake of multifunctional nonbiogenic nanoparticles (fluorescent, superparamagnetic) by spicule-forming cells of bioreactor-cultivated sponge primmorphs provides access to spiculogenesis. The ingested nan…

ScaffoldbiologyChemistryNanoparticleBioengineeringNanotechnologySilicon Dioxidebiology.organism_classificationApplied Microbiology and BiotechnologyFluorescencePoriferaSynthetic biologySpongeBioreactorsSponge spiculeMagnetsAnimalsMagnetic Iron Oxide NanoparticlesSynthetic BiologyHybrid materialFluorescent DyesBiotechnologySuperparamagnetismBiotechnology and Bioengineering
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Eutectogels: Materials for Environmental Recovery

Settore CHIM/06 - Chimica OrganicaDeep eutectic solvents supramolecular gels dyes removal
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Dye selection for live cell imaging of intact siRNA

2011

Abstract Investigations into the fate of small interfering RNA (siRNA) after transfection may unravel new ways to improve RNA interference (RNAi) efficiency. Because intracellular degradation of RNA may prevent reliable observation of fluorescence-labeled siRNA, new tools for fluorescence microscopy are warranted to cover the considerable duration of the RNAi effect. Here, the characterization and application of new fluorescence resonance energy transfer (FRET) dye pairs for sensing the integrity of duplex siRNA is reported, which allows an assessment of the degradation status of an siRNA cell population by live cell imaging. A panel of high-yield fluorescent dyes has been investigated for …

Small interfering RNACell SurvivalClinical BiochemistryPopulationBiologyBiochemistryLive cell imagingRNA interferenceFluorescence Resonance Energy TransferFluorescence microscopeAnimalsRNA Small InterferingeducationMolecular BiologyCells CulturedFluorescent Dyeseducation.field_of_studyMicroscopy ConfocalBrainEndothelial CellsRNATransfectionHydrogen-Ion ConcentrationMolecular biologyRatsFörster resonance energy transferBiophysicsBiological Chemistry
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Flow cytometric kinetic assay of the activity of Na+/H+ antiporter in mammalian cells.

2004

Background The Na+/H+ exchanger (NHE) of mammalian cells is an integral membrane protein that extrudes H+ ion in exchange for extracellular Na+ and plays a crucial role in the regulation of intracellular pH (pHi). Thus, when pHi is lowered, NHE extrudes protons at a rate depending of pHi that can be expressed as pH units/s. Methods To abolish the activity of other cellular pH-restoring systems, cells were incubated in bicarbonate-free Dulbecco's modified Eagle's medium buffered with HEPES. Flow cytometry was used to determine pHi with 2′,7′-bis-(2-carboxyethyl)-5-(and-6)-carboxyfluorescein acetoxymethyl ester or 5-(and-6)-carboxy SNARF-1 acetoxymethyl ester acetate, and the appropriate fluo…

Sodium-Hydrogen ExchangersTime FactorsNigericinIntracellular pHBiophysicsIonophoreNaphtholsBiochemistryModels BiologicalPathology and Forensic MedicineFlow cytometryCell Linechemistry.chemical_compoundJurkat CellsMiceEndocrinologyChondrocytesIschemiamedicineExtracellularAnimalsHumansBenzopyransMuscle SkeletalCells CulturedFluorescent DyesHEPESmedicine.diagnostic_testDose-Response Relationship DrugRhodaminesCell BiologyHematologyHydrogen-Ion ConcentrationFlow CytometryFluoresceinsAmilorideKineticsBiochemistrychemistryCell cultureCalibrationNIH 3T3 Cellsmedicine.drugCytometry. Part A : the journal of the International Society for Analytical Cytology
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The origin of slow electron recombination processes in dye-sensitized solar cells with alumina barrier coatings

2004

We investigate the effect of a thin alumina coating of nanocrystalline TiO2 films on recombination dynamics of dye-sensitized solar cells. Both coated and uncoated cells were measured by a combination of techniques: transient absorption spectroscopy, electrochemical impedance spectroscopy, and open-circuit voltage decay. It is found that the alumina barrier reduces the recombination of photoinjected electrons to both dye cations and the oxidized redox couple. It is proposed that this observed retardation can be attributed primarily to two effects: almost complete passivation of surface trap states in TiO2 that are able to inject electrons to acceptor species, and slowing down by a factor of…

Solar cellsCharge injectionPassivationAbsorption spectroscopyIon recombinationThin filmsAluminaAnalytical chemistryGeneral Physics and AstronomyPhotochemistryTime resolved spectraTitanium compounds ; Alumina ; Nanostructured materials ; Semiconductor materials ; Thin films ; Solar cells ; Ion recombination ; Dyes ; Charge exchange ; Charge transfer states ; Charge injection ; Electrochemical impedance spectroscopy ; Time resolved spectraSemiconductor materials:FÍSICA [UNESCO]Ultrafast laser spectroscopyCharge exchangeThin filmSpectroscopyDyesQCChemistryUNESCO::FÍSICANanostructured materialsAcceptorDielectric spectroscopyDye-sensitized solar cellTACharge transfer statesTitanium compoundsElectrochemical impedance spectroscopy
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2-D differential membrane proteome analysis of scarce protein samples

2006

Proteome studies with small sample amounts are difficult to perform, especially when membrane proteins are the focus of interest. In our study a new method for the analysis of scarce membrane protein samples combining large gel 2-D-CTAB/SDS-PAGE with fluorescence dye saturation labelling (satDIGE) was developed, allowing a highly sensitive differential analysis of different cell states. After Triton X-114 phase partitioning, enriched membrane protein samples of T cells were labelled at cysteine residues using fluorescence dyes and separated by large gel 2D-CTAB/SDS-PAGE. For a differential analysis 3 mug protein was found to be sufficient to detect proteins in a widespread well-separated di…

Spectrometry Mass Electrospray IonizationChromatographyProteomeMolecular Sequence DataCellMembrane ProteinsBiologyProteomicsBiochemistryFluorescenceMicemedicine.anatomical_structureMembrane proteinLabellingProteomemedicineAnimalsHumansElectrophoresis Gel Two-DimensionalAmino Acid SequenceMolecular BiologyPeptide sequenceCells CulturedFluorescent DyesCysteinePROTEOMICS
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Azo-Sulforhodamine Dyes: A Novel Class of Broad Spectrum Dark Quenchers

2014

A rapid access to a novel class of water-soluble dark quencher dyes was achieved using an azo-coupling reaction between a fluorescent primary arylamine derived from a sulforhodamine 101 scaffold and a tertiary aniline equipped with different bioconjugatable groups. The thus obtained nonfluorescent azo-sulforhodamine hybrids display a broad quenching range spanning the visible to NIR regions. This was demonstrated through the preparation and enzymatic activation of FRET-based fluorogenic substrates of urokinase.

Spectrophotometry InfraredPhotochemistryBiochemistryBroad spectrumchemistry.chemical_compoundAnilineRapid accessDark quencher[CHIM]Chemical SciencesPhysical and Theoretical ChemistryColoring AgentsComputingMilieux_MISCELLANEOUSFluorescent DyesAniline CompoundsQuenching (fluorescence)Molecular StructureRhodaminesOrganic ChemistryWaterSulforhodamine 101Fluorescence3. Good healthFörster resonance energy transferSolubilitychemistryAzo Compounds
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Synthesis of platinum complexes with 2-(5-perfluoroalkyl-1,2,4-oxadiazol-3yl)-pyridine and 2-(3-perfluoroalkyl-1-methyl-1,2,4-triazole-5yl)-pyridine …

2016

Five new mononuclear Pt(II) complexes with 5-perfluoroalkyl-1,2,4-oxadiazolyl-pyridine and 3-perfluoroalkyl-1,2,4-triazolyl-pyridine ligands are reported. The ligands 2-(5-perfluoroheptyl-1,2,4-oxadiazole-3yl)-pyridine (pfhop), 2-(5-perfluoropropyl)-1,2,4-oxadiazole-3yl)-pyridine (pfpop), 2-(3-perfluoroheptyl-1-methyl-1,2,4-triazole-5yl)-pyridine (pfhtp), 2-(3-perfluoropropyl-1-methyl-1,2,4-triazole-5yl)-pyridine (pfptp) and their complexes [PtCl2(pfhop)(2)]center dot 1.5 DMSO (2a), [PtCl2(pfpop)(2)]center dot 1.5 DMSO (3a), [PtCl2(pfhtp)(2)]center dot 1.5 DMSO (4a), PtCl2(pfhtp) (4b), [PtCl2(PfPtP)(2)]center dot 1.5 DMSO (5a) have been synthesized and structurally characterized. The comple…

Spectrophotometry InfraredStereochemistryPyridinesProton Magnetic Resonance SpectroscopyTriazoleOxadiazoleAntineoplastic AgentsApoptosisPlatinum Compounds010402 general chemistryLigands01 natural sciencesBiochemistryInorganic Chemistrychemistry.chemical_compoundSettore BIO/10 - BiochimicaCell Line TumorEthidiumPyridineMoleculeHumansFluorescent DyesPlatinum complexes oxadiazole antitumor activity010405 organic chemistryLigandAcridine orange124-TriazoleSettore CHIM/06 - Chimica OrganicaAcridine Orange0104 chemical scienceschemistrySettore CHIM/03 - Chimica Generale E InorganicaEthidium bromideJournal of inorganic biochemistry
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