Search results for "Resonance energy transfer"

showing 10 items of 98 documents

Dendron to central core S1-S1 and S2-S(n) (n1) energy transfers in artificial special pairs containing dendrimers with limited numbers of conformatio…

2013

Two dendrimers consisting of a cofacial free-base bisporphyrin held by a biphenylene spacer and function- alized with 4-benzeneoxomethane (5-(4-benzene)tri-10,15,20-(4-n-octyl- benzene)zinc(II)porphyrin) using either five or six of the six available meso-positions, have been synthesized and characterized as models for the an- tenna effect in Photosystems I and II. The presence of the short linkers, -CH2O-, and long C8H17 soluble side chains substantially reduces the number of conformers (foldamers) compared with classic dendrimers built with longer flexible chains. This simpli- fication assists in their spectroscopic and photophysical analysis, notably with respect to fluorescence resonance…

AnthracenesDendrimersMolecular StructureStereochemistryMetalloporphyrinsOrganic ChemistryGeneral ChemistryBiphenylenePorphyrinFluorescenceAcceptorCatalysischemistry.chemical_compoundCrystallographyFörster resonance energy transferchemistryEnergy TransferModels ChemicalDendrimerSinglet stateConformational isomerismChemistry (Weinheim an der Bergstrasse, Germany)
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Development of fluorogenic probe-based PCR assays for the detection and quantification of bovine piroplasmids.

2009

This paper reports two new quantitative PCR (qPCR) assays, developed in an attempt to improve the detection of bovine piroplasmids. The first of these techniques is a duplex TaqMan assay for the simultaneous diagnosis of Babesia bovis and B. bigemina. This technique is ideal for use in South America where bovids harbour no theilerids. The second technique, which is suitable for the diagnosis of both babesiosis and theileriosis worldwide, involves fluorescence resonance energy transfer (FRET) probes. In FRET assays, Babesia bovis, B. divergens, Babesia sp. (B. major or B. bigemina), Theileria annae and Theileria sp. were all identifiable based on the melting temperatures of their amplified f…

BabesiaPolymerase Chain ReactionSensitivity and Specificitylaw.inventionlawBabesiosisTheileriaTheileriaFluorescence Resonance Energy TransferTaqManmedicineAnimalsHorsesBabesia bigeminaPolymerase chain reactionGeneral VeterinarybiologyReproducibility of ResultsBabesia bovisBabesiosisGeneral MedicineDNA Protozoanbiology.organism_classificationmedicine.diseaseVirologyMolecular biologyBabesiaTheileria Quantitative PCR Molecular diagnostic TaqMan probes FRET probesTheileriasisReal-time polymerase chain reactionBabesiaCattleHorse DiseasesParasitology
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Development of Polyamine‐Substituted Triphenylamine Ligands with High Affinity and Selectivity for G‐Quadruplex DNA

2019

Currently, significant efforts are devoted to designing small molecules able to bind selectively to guanine quadruplexes (G4s). These noncanonical DNA structures are implicated in various important biological processes and have been identified as potential targets for drug development. Previously, a series of triphenylamine (TPA)-based compounds, including macrocyclic polyamines, that displayed high affinity towards G4 DNA were reported. Following this initial work, herein a series of second-generation compounds, in which the central TPA has been functionalised with flexible and adaptive linear polyamines, are presented with the aim of maximising the selectivity towards G4 DNA. The acid-bas…

Biochemistry & Molecular BiologyCircular dichroismChemistry Medicinal0601 Biochemistry and Cell BiologyLigands010402 general chemistryTriphenylamineG-quadruplex01 natural sciencesBiochemistryFluorescence spectroscopyStructure-Activity Relationshipchemistry.chemical_compoundFluorescence Resonance Energy TransferPolyaminesPharmacology & PharmacyCOORDINATION CHEMISTRYPROBEMolecular BiologyScience & Technology0304 Medicinal and Biomolecular Chemistry010405 organic chemistryOrganic ChemistryDNACombinatorial chemistrySmall molecule0104 chemical sciences* G-quadruplex DNA * G4 selectivity * polyamine-based ligand *fluorescenceG-QuadruplexesFörster resonance energy transferchemistryDrug DesignFRETEQUILIBRIUM-CONSTANTSMolecular MedicineCOMPLEXESfluorescenceEMISSIONSelectivityLife Sciences & BiomedicineDNAChemBioChem
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Exosome-associated polysialic acid modulates membrane potentials, membrane thermotropic properties, and raft-dependent interactions between vesicles.

2020

In mammals, polysialic acid (polySia) attached to a small number of transmembrane protein carriers occurs on the surface of plasma membranes of neural, cancer, immune, and placental trophoblast cells. Here, our goal was to demonstrate the presence of polySia on exosomes and its effect on membrane properties. We isolated exosomes and found that polysialylated exosomes in fetal bovine serum originate mostly from placental trophoblasts, while in calf bovine serum, they originate from immune cells. Enzymatic removal of polySia chains from the exosomal surface makes the membrane surface potential more positive, transmembrane potential more negative, and reduces the activation energy for membrane…

BiophysicsExosomesBiochemistryExosomeMembrane Potentials03 medical and health sciencesMembrane MicrodomainsStructural BiologyCell Line TumorGeneticsFluorescence Resonance Energy TransferHumansMolecular Biology030304 developmental biologyMembrane potential0303 health sciencesPolysialic acidChemistryVesicle030302 biochemistry & molecular biologyTemperatureCell BiologyMicrovesiclesTransmembrane proteinCell biologyMembraneSialic AcidsAnisotropyanisotropy; exosomes; FRET; membrane potentials; polysialicacid; raftsFetal bovine serumFEBS lettersReferences
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Live cell imaging of duplex siRNA intracellular trafficking.

2015

Intracellular distribution of siRNA after in vitro transfection typically depends on lipopolyplexes, which must release the siRNA into the cytosol. Here, the fate of siRNAs was monitored by FRET-based live cell imaging. Subsequent to in situ observation of uptake and release processes, this approach allowed the observation of a number of hitherto uncharacterized intracellular distribution and degradation processes, commencing with a burst of endosomal releases, followed, in some cases, by fast siRNA influx into the nucleus. The continued observation of intact siRNA against a background of free fluorophores resulting from advanced degradation was possible by a specifically developed imaging …

Cell NucleusSmall interfering RNAMicroscopy ConfocalEndosomeTransfectionEndosomesBiologyTransfectionRNA TransportCell biologyCell LineRatsCytosolLive cell imagingCell cultureRNA interferenceGeneticsFluorescence Resonance Energy TransferAnimalsRNARNA Small InterferingIntracellularNucleic acids research
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Quantitative characterization of tetraspanin 8 homointeractions in the plasma membrane

2021

The spatial distribution of proteins in cell membranes is crucial for signal transduction, cell communication and membrane trafficking. Members of the Tetraspanin family organize functional protein clusters within the plasma membrane into so-called Tetraspanin-enriched microdomains (TEMs). Direct interactions between Tetraspanins are believed to be important for this organization. However, studies thus far have utilized mainly co-immunoprecipitation methods that cannot distinguish between direct and indirect, through common partners, interactions. Here we study Tetraspanin 8 homointeractions in living cells via quantitative fluorescence microscopy. We demonstrate that Tetraspanin 8 exists i…

Cell signalingTetraspaninsLipoylationDimerTransfectionBiochemistryArticleProtein–protein interactionchemistry.chemical_compoundMembrane MicrodomainsTetraspaninFluorescence Resonance Energy TransferHumansMolecular BiologyChemistryCell BiologyDissociation constantHEK293 CellsMembraneMicroscopy FluorescenceMembrane proteinembryonic structuresBiophysicsThermodynamicsProtein MultimerizationSignal transductionSignal TransductionBiochemical Journal
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Parallelized TCSPC for dynamic intravital fluorescence lifetime imaging : quantifying neuronal dysfunction in neuroinflammation

2013

Two-photon laser-scanning microscopy has revolutionized our view on vital processes by revealing motility and interaction patterns of various cell subsets in hardly accessible organs (e.g. brain) in living animals. However, current technology is still insufficient to elucidate the mechanisms of organ dysfunction as a prerequisite for developing new therapeutic strategies, since it renders only sparse information about the molecular basis of cellular response within tissues in health and disease. In the context of imaging, Forster resonant energy transfer (FRET) is one of the most adequate tools to probe molecular mechanisms of cell function. As a calibration-free technique, fluorescence lif…

Central Nervous SystemDiagnostic ImagingFluorescence-lifetime imaging microscopyPathologymedicine.medical_specialtyMouseScienceBiophysicsMedizinNeurophysiologyContext (language use)NeuroimagingBiosensing TechniquesBiologyIn Vitro TechniquesMiceCalcium imagingModel OrganismsMicroscopyMolecular Cell BiologyNeurobiology of Disease and RegenerationMedical imagingmedicineFluorescence Resonance Energy TransferAnimalsBiologyNeuroinflammationMultidisciplinaryPhysicsQRBrainAnimal ModelsIntravital ImagingCalcium ImagingFörster resonance energy transferMedicineCalciumFunction and Dysfunction of the Nervous SystemNeuroscienceResearch ArticleNeuroscience
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Comparison of quantum dot-binding protein tags: Affinity determination by ultracentrifugation and FRET

2013

Abstract Background Hybrid complexes of proteins and colloidal semiconductor nanocrystals (quantum dots, QDs) are of increasing interest in various fields of biochemistry and biomedicine, for instance for biolabeling or drug transport. The usefulness of protein–QD complexes for such applications is dependent on the binding specificity and strength of the components. Often the binding properties of these components are difficult and time consuming to assess. Methods In this work we characterized the interaction between recombinant light harvesting chlorophyll a / b complex (LHCII) and CdTe/CdSe/ZnS QDs by using ultracentrifugation and fluorescence resonance energy transfer (FRET) assay exper…

ChemistryBinding proteinBiophysicsNanoparticleProtein tagBiochemistryCrystallographyB vitaminsFörster resonance energy transferQuantum dotQuantum DotsFluorescence Resonance Energy TransferNanoparticlesUltracentrifugeChlorophyll Binding ProteinsUltracentrifugationMolecular BiologyBinding selectivityProtein BindingBiochimica et Biophysica Acta (BBA) - General Subjects
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Three-dimensional orientational colocalization of individual donor--acceptor pairs.

2004

We report on the determination of the three-dimensional orientation of the donor and acceptor transition dipoles in individual fluorescence resonance energy transfer (FRET) pairs by means of scanning optical microscopy with annular illumination. Knowledge of the mutual orientation of the donor and acceptor dipole is mandatory for reliable distance determination based on FRET efficiency measurements. In our model system perylenediimide as the donor and terryelenediimide as the acceptor are coupled via a stiff p-terphenyl linker. The absorption dipoles of the donor and acceptor are selectively addressed by the 488 nm and 647 line of an Ar/Kr mixed gas laser, respectively. A clear deviation fr…

ChemistryGeneral Physics and AstronomyLaserFluorescenceAcceptorMolecular physicslaw.inventionDipoleCrystallographyFörster resonance energy transferOptical microscopelawPhysical and Theoretical ChemistryAbsorption (electromagnetic radiation)LinkerThe Journal of chemical physics
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Filling the “green gap” of the major light-harvesting chlorophyll a/b complex by covalent attachment of Rhodamine Red

2009

AbstractThe major light-harvesting chlorophyll a/b complex (LHCII) greatly enhances the efficiency of photosynthesis in green plants. Recombinant LHCII can be assembled in vitro from its denatured, bacterially expressed apoprotein and plant pigments. This makes it an interesting candidate for biomimetic light-harvesting in photovoltaic applications. Due to its almost 20 pigments bound per apoprotein, LHCII absorbs efficiently in the blue and red spectral domains of visible light but less efficiently in the green domain, the so-called “green gap” in its absorption spectrum. Here we present a hybrid complex of recombinant LHCII with organic dyes that add to LHCII absorption in the green spect…

ChlorophyllLHCIIProtein FoldingFRET (Förster resonance energy transfer)Chlorophyll aAbsorption spectroscopyBiophysicsPhotosynthesisPhotochemistryBiochemistryRhodamineLight-harvesting complexchemistry.chemical_compoundPhotosynthesisFluorescent DyesRhodaminesChlorophyll Afood and beveragesSite-specific labelingCell BiologyMaleimide dyeB vitaminsSolar spectrumchemistryChlorophyllVisible spectrumBiochimica et Biophysica Acta (BBA) - Bioenergetics
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