Search results for "Fluorescence"

showing 10 items of 2463 documents

Thermo- and light responsive micellation of azobenzene containing block copolymers

2010

In this communication, the synthesis and characterization of thermo- and light responsive block copolymers is reported. PEO-b-PNIPAM polymers with azobenzene moieties were prepared and analyzed by turbidimetry, fluorescence, NMR and DLS measurements. A temperature controlled reversible formation as well as a light induced disruption and reformation of micellar structures in water was found.

chemistry.chemical_classificationMaterials scienceeducationtechnology industry and agricultureMetals and Alloysmacromolecular substancesGeneral ChemistryPolymerFluorescenceCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundLight responsivechemistryAzobenzeneChemical engineeringPolymer chemistryMaterials ChemistryCeramics and CompositesLight inducedCopolymerTurbidimetryChemical Communications
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Analysis of Subcellular Components by Fluorescent-Lectin Binding and Flow Cytometry

2003

Because of their extensive availability and the wide spectrum of carbohydrates that may be specifically bound, lectins have become essential reagents for detection and quantitation of glycoconjugates in solution and in cell surfaces, identification and separation of cells, and functional studies based on membrane properties (1,2).

chemistry.chemical_classificationMembranechemistryBiochemistrymedicine.diagnostic_testGlycoconjugateLectin bindingmedicineFunctional studiesFluorescenceFlow cytometry
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Determining sulfur-containing amino acids by capillary electrophoresis: A fast novel method for total homocyst(e)ine human plasma

1999

A high-performance capillary electrophoresis (HPCE) method based on laser-induced fluorescence detection is presented here. It enables the determination of sulfur-containing amino acids within 15 min. Fluorescence of sulfur-containing amino acids in plasma is linear over a range of 50-150 micromol/L for L-methionine, 5-100 micromol/L for L-homocysteine, and 50-200 micromol/L for L-cysteine. For homocysteine, we were able to detect 1 fmol injected, equivalent to a plasma concentration of 10 nmol/L. A similar sensitivity is present for cysteine, an even lower one being found for methionine. The intra- and interassay relative standard deviations are < 1%. High-performance liquid chromatography…

chemistry.chemical_classificationMethionineChromatographyMolecular StructureHomocysteineClinical BiochemistryElectrophoresis Capillarychemistry.chemical_elementBiochemistrySulfurFluorescenceHigh-performance liquid chromatographyAnalytical ChemistryAmino acidchemistry.chemical_compoundCapillary electrophoresischemistryHumansAmino AcidsHomocysteineChromatography High Pressure LiquidSulfurCysteineElectrophoresis
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Dominance of Chain Entanglement over Transient Sticking on Chain Dynamics in Hydrogen-Bonded Supramolecular Polymer Networks in the Melt

2018

The chain dynamics in supramolecular polymer networks is determined by the interplay of the kinetics of transient interchain association and relaxation of the network chains themselves. This interplay can be addressed by studying model supramolecular polymer networks in which the number of associative side groups and the molar mass of the covalently jointed backbone polymers are both varied systematically. To realize this idea, we use precursor chains with three different molar masses, which comes along with different extents of entanglement in the melt state. For each molar mass, the precursor polymers are functionalized with three different relative contents of associative side groups, gi…

chemistry.chemical_classificationMolar massMaterials sciencePolymers and PlasticsOrganic ChemistryKineticsFluorescence recovery after photobleaching02 engineering and technologyQuantum entanglementPolymer010402 general chemistry021001 nanoscience & nanotechnologyThermal diffusivity01 natural sciences0104 chemical sciencesInorganic ChemistrySupramolecular polymerschemistryChemical physicsCovalent bondMaterials Chemistry0210 nano-technologyMacromolecules
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Fluorescence Correlation Spectroscopy in Dilute Polymer Solutions: Effects of Molar Mass Dispersity and the Type of Fluorescent Labeling

2015

Fluorescence correlation spectroscopy (FCS) has become an important tool in polymer science. Among various other applications the method is often applied to measure the hydrodynamic radius and the degree of fluorescent labeling of polymers in dilute solutions. Here we show that such measurements can be strongly affected by the molar mass dispersity of the studied polymers and the way of labeling. As model systems we used polystyrene and poly(methyl methacrylate) synthesized by atom transfer radical polymerization or free-radical polymerization. Thus, the polymers were either end-labeled bearing one fluorophore per chain or side-labeled with a number of fluorophores per chain proportional to…

chemistry.chemical_classificationMolar massPolymers and PlasticsAtom-transfer radical-polymerizationOrganic ChemistryDispersityAnalytical chemistryFluorescence correlation spectroscopyPolymerDegree of polymerizationInorganic ChemistrychemistryPolymerizationMaterials ChemistryMolar mass distributionACS Macro Letters
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Cluster dirhenium(III) cis-dicarboxylates with α-amino acids ligands as mighty selective G4s binders.

2021

The synthesis of four dirhenium(III) cis-dicarboxylates with the α-amino acids residues Asp (I), Glu (II), Phe (III) and Tyr (IV) is presented. The G-quadruplex stabilization potential was evaluated by fluorescence resonance energy transfer - melting analysis. All derivatives show specific binding to c-kit1 quadruplex, while II and IV have also strong stabilization activity to HTelo21 quadruplex. At the same time, the compounds do not show any stabilization activity for ds26 DNA, which suggests unique mechanisms of molecular DNA recognition for these complexes.

chemistry.chemical_classificationMolecular StructureStereochemistrychemistry.chemical_elementDNARheniumG-quadruplexLigandsBiochemistryAmino acidInorganic ChemistryG-Quadruplexeschemistry.chemical_compoundFörster resonance energy transferRheniumchemistryCoordination ComplexesCluster (physics)Fluorescence Resonance Energy TransferHumansheterocyclic compoundsAmino AcidsDNADna recognitionJournal of inorganic biochemistry
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Polymeric gegenions induced variability and mobility of amphiphilic supramolecular structures on solid substrates

1992

Abstract The micromorphological variations of amphiphilic L -glutamate derivatives at air-substrate interfaces due to an adjacent mobile polymer matrix have been investigated via fluorescence microscopy. Adjusted monolayers of the L -glutamate derivatives have been transferred by LB technique out of different aggregation states onto various substrates. The substrates have been prepared by successive polymer preadsorption to the solid support. The influence of the adjacent polymer layers on the domain morphology as a function of water content and temperature has been examined intensively. Moreover, reversible domain changes induced by temperature variation of the transferred films have been …

chemistry.chemical_classificationMorphology (linguistics)Metals and AlloysAnalytical chemistryFluorescence spectrometrySupramolecular chemistrySurfaces and InterfacesPolymerSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMatrix (chemical analysis)chemistryChemical engineeringAmphiphileMonolayerMaterials ChemistryFluorescence microscopeThin Solid Films
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Imaging of Keratin Dynamics during the Cell Cycle and in Response to Phosphatase Inhibition

2004

Publisher Summary The characterization and development of autofluorescent proteins, most prominently of the green florescent protein, have provided tools to label cellular structures such that they can be examined in living cells. This chapter highlights the potential of live cell imaging in providing novel and unprecedented insights into the dynamic organization of the keratin cytoskeleton and outlines the important aspects of this method. The live cell imaging experiments suggest that the driving force behind the vectorial and dynamic keratin distribution patterns relies both on microtubules and microfilaments and their associated factors. The studies on the dynamics of the keratin cytosk…

chemistry.chemical_classificationMotor proteinchemistryLive cell imagingMicrotubuleKeratinFluorescence recovery after photobleachingmacromolecular substancesBiologyIntermediate filamentCytoskeletonMicrofilamentCell biology
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The triplet excited state of the biocative compound thiabendazole. Characterization and suitability as reporter for cyclodextrin complexation

2012

Fluorescence spectroscopy, laser flash photolysis (LPF), and density functional theory calculations have been performed to characterize the photobehavior of thiabendazole (1). Direct LFP of 1 results in the generation of a transient absorbing at λmax = 570 nm identified as the triplet excited state (31∗). The intersystem crossing quantum yield is 0.91, and the triplet energy is 288 kJ mol−1. The singlet–triplet energy gap is 84 kJ mol−1. The behavior of thiabendazole within CDs results in a marked enhancement of the triplet lifetime, this change is attributed to the mobility restrictions of included 1 imposed by the cyclodextrin cavities.

chemistry.chemical_classificationOptimizationCyclodextrinBeta-CyclodextrinGeneral Physics and AstronomyQuantum yieldHuman-SerumDensityProteinsPhotochemistryPolarizable continuum modelBenzimidazoleFluorescence spectroscopyIntersystem crossingQUIMICA ORGANICAchemistryExcited stateSolventTransitionFlash photolysisPolarizable continuum modelDensity functional theoryPhysical and Theoretical ChemistryApproximation
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Comparative analysis of the coordinated motion of Hsp70s from different organelles observed by single-molecule three-color FRET.

2021

Cellular function depends on the correct folding of proteins inside the cell. Heat-shock proteins 70 (Hsp70s), being among the first molecular chaperones binding to nascently translated proteins, aid in protein folding and transport. They undergo large, coordinated intra- and interdomain structural rearrangements mediated by allosteric interactions. Here, we applied a three-color single-molecule Forster resonance energy transfer (FRET) combined with three-color photon distribution analysis to compare the conformational cycle of the Hsp70 chaperones DnaK, Ssc1, and BiP. By capturing three distances simultaneously, we can identify coordinated structural changes during the functional cycle. Be…

chemistry.chemical_classificationOrganellesMultidisciplinarySaccharomyces cerevisiae ProteinsAllosteric regulationPeptideSaccharomyces cerevisiaeBiological SciencesMitochondrial Membrane Transport ProteinsRecombinant ProteinsSingle Molecule ImagingFolding (chemistry)Förster resonance energy transferchemistryHeat shock proteinBiophysicsEscherichia coliFluorescence Resonance Energy TransferMoleculeProtein foldingNucleotideHSP70 Heat-Shock ProteinsMolecular ChaperonesProceedings of the National Academy of Sciences of the United States of America
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