Search results for "Fluorescent"

showing 10 items of 863 documents

A micellar multitasking device: sensing pH windows and gauging the lipophilicity of drugs with fluorescent signals.

2010

A multitasking fluorescent device can be obtained by forming micelles of Triton X-100, containing a lipophilic macrocyclic Cu(2+) complex and the coordinating fluorophore Coumarin 343 (C343), which features a COOH moiety. At low pH the two micellised components do not interact, and the fluorescence of Courmarin 343 (C343) is intense. At intermediate pH, C343 is deprotonated and coordinates to the Cu(2+) centre in its apical position, with fluorescence quenching. At higher pH the deprotonated C343 is displaced from Cu(2+) by the formation of an OH(-) complex, and the fluorescence is revived. This allows the system to carry out its first task as it behaves as an "on-off-on" fluorescent sensor…

FluorophoreStereochemistryOctoxynolKineticsself-assembled devices010402 general chemistry01 natural sciencesMicelleCatalysisFluorescencechemistry.chemical_compoundfluorescent probesCoumarins[ CHIM.OTHE ] Chemical Sciences/OtherlipophilicityMoietyCarboxylateComputingMilieux_MISCELLANEOUSMicelles010405 organic chemistryChemistryOrganic ChemistryAnti-Inflammatory Agents Non-SteroidalAnticoagulantsWaterGeneral ChemistryHydrogen-Ion ConcentrationFluorescence0104 chemical sciencesPartition coefficientCrystallographyKineticsSpectrometry FluorescencepH windowsLipophilicity[CHIM.OTHE]Chemical Sciences/OtherChemistry (Weinheim an der Bergstrasse, Germany)
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A fluorescent molecular sensor for pH windows in traditional and polymeric biocompatible micelles: comicellization of anionic species to shift and re…

2011

A new approach is presented to obtain fluorescent sensors for pH windows that work in water and under biomimetic conditions. A single molecule that features all-covalently linked components is used, thus making it capable of working as a fluorescent sensor with an OFF/ON/OFF response to pH value. The components are a tertiary amine, a pyridine, and a fluorophore (pyrene). The forms with both protonated bases or both neutral bases quench the pyrene fluorescence, whereas the form with the neutral pyridine and protonated amine groups is fluorescent. The molecular sensor is also equipped with a long alkyl chain to make it highly hydrophobic in all its protonated and unprotonated forms, that is,…

FluorophoreTertiary aminePolymersPyridinesInorganic chemistryPhotochemistryMicelleCatalysisPolystyrene sulfonatechemistry.chemical_compoundAmphiphileAminesAlkylMicellesFluorescent Dyeschemistry.chemical_classificationPyrenesfluorescence micelles polymerization potentiometry sensorsOrganic ChemistryMolecular sensorGeneral ChemistryHydrogen-Ion ConcentrationPolyelectrolyteKineticschemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoHydrophobic and Hydrophilic InteractionsChemistry (Weinheim an der Bergstrasse, Germany)
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Gold(I)-Coumarin-Caffeine-Based Complexes as New Potential Anti-Inflammatory and Anticancer Trackable Agents.

2018

Three new gold(I)-coumarin-based trackable therapeutic complexes and two non-trackable analogues have been synthesised and fully characterised. They all display anti-proliferative properties on several types of cancer cell lines, including those of colon, breast, and prostate. Two complexes displayed significant anti-inflammatory effects; one displayed pro-inflammatory behaviour; this highlights the impact of the position of the fluorophore on the caffeine scaffold. Additionally, the three coumarin derivatives could be visualised in vitro by two-photon microscopy.

Fluorophoremedicine.drug_classUltraviolet RaysAnti-Inflammatory AgentsAntineoplastic Agents010402 general chemistry01 natural sciencesBiochemistryAnti-inflammatoryFluorescencechemistry.chemical_compoundCoordination ComplexesCoumarinsCaffeineCell Line TumorDrug DiscoverymedicineHumansGeneral Pharmacology Toxicology and PharmaceuticsFluorescent DyesPharmacology010405 organic chemistryOrganic ChemistryCancerCoumarinmedicine.diseaseCombinatorial chemistryIn vitro0104 chemical sciencesHEK293 CellsMicroscopy Fluorescence MultiphotonchemistryMolecular MedicineGoldCancer cell linesCaffeineChemMedChem
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A novel method for determination of inorganic polyphosphates using the fluorescent dye fura-2.

1997

A method for determining inorganic polyphosphate, which is based on the Mn2+-induced quenching of the fluorescence of the calcium indicator fura-2, is described. The effect of Mn2+ ions on fura-2 fluorescence is gradually abolished in the presence of increasing concentrations of polyphosphate; this allows the quantification both of synthetic polyphosphates and of the naturally occurring polymer isolated from tissues or cells. The described method has some advantages compared to conventional procedures for detection of polyphosphates based on the metachromatic effect on toluidine blue. It can be applied for the determination of pyrophosphate, tripolyphosphate and other short-chain polyphosph…

Fura-2Inorganic chemistryBiophysicsBiochemistryPyrophosphateFluorescencechemistry.chemical_compoundPolyphosphatesAnimalsHumansToluidineMolecular BiologyFluorescent DyesPyrophosphataseManganeseQuenching (fluorescence)ChromatographyPolyphosphateMetachromasiaCell BiologyFluorescenceRatsSpectrometry FluorescencechemistryFura-2HeLa CellsAnalytical biochemistry
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RAB3GAP1 and RAB3GAP2 modulate basal and rapamycin-induced autophagy

2014

Macroautophagy is a degradative pathway that sequesters and transports cytosolic cargo in autophagosomes to lysosomes, and its deterioration affects intracellular proteostasis. Membrane dynamics accompanying autophagy are mostly elusive and depend on trafficking processes. RAB GTPase activating proteins (RABGAPs) are important factors for the coordination of cellular vesicle transport systems, and several TBC (TRE2-BUB2-CDC16) domain-containing RABGAPs are associated with autophagy. Employing C. elegans and human primary fibroblasts, we show that RAB3GAP1 and RAB3GAP2, which are components of the TBC domain-free RAB3GAP complex, influence protein aggregation and affect autophagy at basal an…

GTPase-activating proteinlipid dropletsrab3 GTP-Binding ProteinsATG16L1DMSO dimethyl sulfoxideFEZ20302 clinical medicineATG autophagy-relatedPhagosomesDAPI 4’ 6-diamidino-2-phenylindoleSQSTM1 sequestosome 1ATG16L1MAP1LC3 microtubule-associated protein 1 light chain 3GFP green fluorescent protein0303 health sciencesGABARAP GABA(A) receptor-associated proteinGTPase-Activating ProteinsCell biologyRAB3GAP1RAB3GAP2RABGAP RAB GTPase activating proteinATG3autophagyCALCOCO2 calcium binding and coiled-coil domain 2Basic Research PaperseV empty vectorATG8ATG5PBS phosphate-buffered salineBiologyPE phosphatidylethanolamineTBC domain TRE2-BUB2-CDC16 domainBAG3GEF guanine nucleotide exchange factor03 medical and health sciencesC. elegans Caenorhabditis elegansAnimalsHumansCaenorhabditis elegansMolecular Biology030304 developmental biologySirolimusDPH 1 6-diphenyl-1 3 5-hexatrieneproteostasisAutophagyBiological TransportCell BiologyFEZ1Bafi bafilomycin A1FEZ fasciculation and elongation protein zetaNBR1 neighbor of BRCA1 gene 1ProteostasissiRNA small interfering RNABSA bovine serum albuminRabLysosomes030217 neurology & neurosurgeryAutophagy
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Quantification of resting myocardial blood flow in a pig model of acute ischemia based on first-pass MRI

2005

Qualitative and semiquantitative contrast-enhanced (CE) dynamic perfusion MRI techniques are established as noninvasive diagnostic means of assessing coronary artery disease. However, to date quantification of myocardial blood flow (MBF) has not reached the same acceptance as MBF quantification with nuclear techniques. To validate quantification of MBF at rest using the extracellular contrast agent (CA) Gd-DTPA, we performed an animal study in a pig model of acute myocardial ischemia. We quantified MBF from MRI data with a mathematical model (MMID4) of the underlying vasculature. These MBF results were subsequently compared with the results from fluorescent microspheres. The study showed a …

Gadolinium DTPAmedicine.medical_specialtyMyocardial ischemiaSwineMyocardial IschemiaContrast MediaStatistics NonparametricAcute ischemiaCoronary artery diseaseFluorescent microspheresCoronary CirculationInternal medicinemedicineAnimalsRadiology Nuclear Medicine and imagingFirst passbusiness.industryPig modelBlood flowmedicine.diseaseMagnetic Resonance ImagingDisease Models AnimalAcute DiseaseCardiologybusinessPerfusioncirculatory and respiratory physiologyMagnetic Resonance in Medicine
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Sinusoidal endothelial cells from guinea pig liver synthesize and secrete cellular fibronectin in vitro.

1987

Endothelial liver cells were obtained from guinea pig by enzymatic digestion and centrifugal elutriation. Cells were cultured on gelatin and fibronectin pretreated culture vessels. Endothelial cells were characterized by phase-contrast microscopy, electron microscopy and the presence of Factor VIII-related antigen. Fibronectin secretion was determined in cell-free supernatants by a sensitive and specific ELISA and localized on fixed cultured cells by immunofluorescence. [35S]Methionine endogeneously labeled fibronectin was immunoprecipitated from supernatants and cellular lysates and displayed on sodium dodecyl sulfate polyacrylamide slab gel electrophoresis. After attachment to the culture…

Gel electrophoresisHepatologymedicine.diagnostic_testbiologyGuinea PigsFluorescent Antibody TechniqueEnzyme-Linked Immunosorbent AssayImmunofluorescenceMolecular biologyIn vitroFibronectinsFibronectinEndothelial stem cellPerisinusoidal spacemedicine.anatomical_structureLiverCell cultureHepatocytemedicinebiology.proteinAnimalsElectrophoresis Polyacrylamide GelFemaleEndotheliumCells CulturedHepatology (Baltimore, Md.)
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Expression of the gene of the alpha-smooth muscle-actin isoform in rat liver and in rat fat-storing (ITO) cells.

1990

Fat storing cells (FSCs) in the liver represent the main site of vitamin A deposition in the body. These cells are considered to play an important role during scar formation and fibrogenesis in the liver. The putative descent of FSCs from the fibroblastic or from the myofibroblastic system have not been determined yet by morphological or immunohistochemical studies. To further define the origin of these liver cells, we analysed the pattern of expression of three structural proteins: vimentin, desmin and the α-smooth muscle (SM)-actin isoform in FSCs of the rat liver, in smooth muscle cells (SMCs) from the aorta and in rat skin fibroblasts. FSCs were studied by immunohistochemical methods im…

Gene isoformPathologymedicine.medical_specialtyFluorescent Antibody TechniqueGene ExpressionVimentinmacromolecular substancesBiologyDesminImmunoenzyme TechniquesNecrosisGene expressionmedicineAnimalsVimentinNorthern blotActinAortaCells CulturedImmunoperoxidaseNucleic Acid HybridizationMuscle SmoothRats Inbred StrainsGeneral MedicineFibroblastsLipid MetabolismMolecular biologyActinsRatsLiverHepatic stellate cellbiology.proteinRNADesminFemaleVirchows Archiv. B, Cell pathology including molecular pathology
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Differential Distribution of Harmonin Isoforms and Their Possible Role in Usher-1 Protein Complexes in Mammalian Photoreceptor Cells

2003

PURPOSE. Human Usher syndrome is the most common form of combined deafness and blindness. Usher type I (USH1), the most severe form, is characterized by profound congenital deafness, constant vestibular dysfunction, and prepubertal onset retinitis pigmentosa. Previous studies have shown that the USH1-proteins myosin VIIa, harmonin, and cadherin 23 interact and form a functional network during hair cell differentiation in the inner ear. The purpose of the present study was to analyze the molecular and cellular functions of these USH1 proteins in the mammalian retina. METHODS. Antibodies to USH1 proteins were generated and used in Western blot analysis of subcellular photoreceptor fractions a…

Gene isoformUsher syndromeBlotting WesternSynaptophysinCell Cycle ProteinsMyosinsBiologyPhotoreceptor cellMiceRetinitis pigmentosaotorhinolaryngologic diseasesmedicineAnimalsProtein IsoformsRats WistarFluorescent Antibody Technique IndirectMicroscopy ImmunoelectronCytoskeletonGeneticsRetinaHair cell differentiationReverse Transcriptase Polymerase Chain ReactionCadherinDyneinsCadherinsmedicine.diseaseeye diseasesRatsCell biologyMice Inbred C57BLCytoskeletal Proteinsmedicine.anatomical_structureMicroscopy FluorescenceMyosin VIIasense organsCarrier ProteinsPhotoreceptor Cells VertebrateSubcellular FractionsInvestigative Opthalmology & Visual Science
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Membrane potential dye imaging of ventromedial hypothalamus neurons from adult mice to study glucose sensing

2013

Studies of neuronal activity are often performed using neurons from rodents less than 2 months of age due to the technical difficulties associated with increasing connective tissue and decreased neuronal viability that occur with age. Here, we describe a methodology for the dissociation of healthy hypothalamic neurons from adult-aged mice. The ability to study neurons from adult-aged mice allows the use of disease models that manifest at a later age and might be more developmentally accurate for certain studies. Fluorescence imaging of dissociated neurons can be used to study the activity of a population of neurons, as opposed to using electrophysiology to study a single neuron. This is par…

General Chemical Engineeringneurons/cytology/metabolism/ physiologystaining and labeling/ methodsventromedial hypothalamic[ SDV.BA ] Life Sciences [q-bio]/Animal biologyMembrane Potentials0302 clinical medicinePremovement neuronal activity[SDV.BDD]Life Sciences [q-bio]/Development BiologyNeuronsMembrane potential0303 health scienceseducation.field_of_studyGeneral Neuroscience[SDV.BA]Life Sciences [q-bio]/Animal biologynucleus/cytology/metabolism/ physiologyanimalsmedicine.anatomical_structureHypothalamus[SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]fluorescent dyes/ chemistryinbred c57blmicePopulationConnective tissuefluorescence/ methodsBiologyGeneral Biochemistry Genetics and Molecular Biologyspectrometry03 medical and health sciencesmaleExtracellularmedicine[ SDV.BDD ] Life Sciences [q-bio]/Development BiologyeducationFluorescent Dyes030304 developmental biologyStaining and LabelingGeneral Immunology and Microbiologymembrane potentials/physiologyMice Inbred C57BLElectrophysiologyGlucoseSpectrometry Fluorescencenervous systemVentromedial Hypothalamic Nucleus[ SDV.NEU ] Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]NeuronNeuroscience030217 neurology & neurosurgeryglucose/ metabolismNeuroscience
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