Search results for "Microscopy."

showing 10 items of 3331 documents

Genesis of amorphous calcium carbonate containing alveolar plates in the ciliate Coleps hirtus (Ciliophora, Prostomatea).

2013

7 pages; International audience; In the protist world, the ciliate Coleps hirtus (phylum Ciliophora, class Prostomatea) synthesizes a peculiar biomineralized test made of alveolar plates, structures located within alveolar vesicles at the cell cortex. Alveolar plates are arranged by overlapping like an armor and they are thought to protect and/or stiffen the cell. Although their morphology is species-specific and of complex architecture, so far almost nothing is known about their genesis, their structure and their elemental and mineral composition. We investigated the genesis of new alveolar plates after cell division and examined cells and isolated alveolar plates by electron microscopy, e…

Biomineralization570Morphology (linguistics)MineralogyColeps hirtus02 engineering and technologyCalcium Carbonatelaw.invention03 medical and health scienceschemistry.chemical_compoundX-Ray DiffractionStructural BiologylawSpectroscopy Fourier Transform InfraredCell cortexCiliophora[SDV.IB.BIO]Life Sciences [q-bio]/Bioengineering/BiomaterialsAlveolar plates030304 developmental biologyCiliate0303 health sciencesProstomateabiologyVesicleCiliateSpectrometry X-Ray Emission500respiratory system021001 nanoscience & nanotechnologybiology.organism_classification[ SDV.IB.BIO ] Life Sciences [q-bio]/Bioengineering/BiomaterialsAmorphous calcium carbonateMicroscopy ElectronchemistryProtozoanBiophysicsAmorphous calcium carbonateElectron microscope0210 nano-technologyBiomineralization
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Temperature-induced microstructural changes in shells of laboratory-grown Arctica islandica (Bivalvia).

2021

Bivalve shells are increasingly used as archives for high-resolution paleoclimate analyses. However, there is still an urgent need for quantitative temperature proxies that work without knowledge of the water chemistry–as is required for δ18O-based paleothermometry–and can better withstand diagenetic overprint. Recently, microstructural properties have been identified as a potential candidate fulfilling these requirements. So far, only few different microstructure categories (nacreous, prismatic and crossed-lamellar) of some short-lived species have been studied in detail, and in all such studies, the size and/or shape of individual biomineral units was found to increase with water temperat…

BiomineralizationAtmospheric Science010504 meteorology & atmospheric sciencesPhysiologyScanning electron microscopeArctica islandica010502 geochemistry & geophysicsBiochemistry01 natural sciencesMachine LearningMaterials PhysicsPhase (matter)Image Processing Computer-AssistedElectron MicroscopyMicrostructureClimatologyMicroscopyMultidisciplinaryAgricultural and Biological Sciences(all)biologyPhysicsQTemperatureREukaryotaSoftware EngineeringMicrostructureAdaptation PhysiologicalDiagenesisPhysical SciencesEngineering and TechnologyMedicineScanning Electron MicroscopyPaleotemperaturePorosityResearch ArticleBivalvesComputer and Information SciencesMaterials scienceBaltic SeaImaging TechniquesScienceMaterials ScienceShell (structure)MineralogyResearch and Analysis MethodsComputer SoftwareAnimal ShellsBodies of waterAnimalsPaleoclimatologyGeneralArctica islandica0105 earth and related environmental sciencesBiochemistry Genetics and Molecular Biology(all)MorphometryOrganismsPaleontologyWaterBiology and Life SciencesMolluscsbiology.organism_classificationBivalviaInvertebratesBivalviaMarine and aquatic sciencesEarth sciencesMicroscopy Electron ScanningLaboratoriesPhysiological ProcessesZoologySoftwareGenetics and Molecular Biology(all)BiomineralizationPLoS ONE
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Direct investigation of viscosity of an atypical inner membrane of Bacillus spores: A molecular rotor/FLIM study

2013

Abstract We utilize the fluorescent molecular rotor Bodipy-C12 to investigate the viscoelastic properties of hydrophobic layers of bacterial spores Bacillus subtilis. The molecular rotor shows a marked increase in fluorescence lifetime, from 0.3 to 4 ns, upon viscosity increase from 1 to 1500 cP and can be incorporated into the hydrophobic layers within the spores from dormant state through to germination. We use fluorescence lifetime imaging microscopy to visualize the viscosity inside different compartments of the bacterial spore in order to investigate the inner membrane and relate its compaction to the extreme resistance observed during exposure of spores to toxic chemicals. We demonstr…

BiophysicsAnalytical chemistryBacillus subtilis010402 general chemistry01 natural sciencesBiochemistryEndosporeMicroviscosity03 medical and health sciencesViscosityLipid bilayer030304 developmental biologySpores Bacterial0303 health sciencesFluorescence Lifetime Imaging (FLIM)biologyViscosityfungiCell BiologyLipid membranesbiology.organism_classification0104 chemical sciencesSporeMicroviscosityMembraneMicroscopy FluorescenceMolecular rotorsBiophysicsBacterial sporeBacillus subtilis sporesBacillus subtilisBiochimica et Biophysica Acta (BBA) - Biomembranes
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Sedimentation properties of chitosomal chitin synthetase from the wild-type strain and the 'slime' variant of Neurospora crassa.

1989

Marked differences in the pattern of sedimentation of cellular structures were observed after isopycnic centrifugation of crude cell-free preparations from the Neurospora crassa wall-less 'slime' variant and mycelial wild-type strain. Kinetic studies of particle sedimentation showed that the various types of subcellular components, as revealed by turbidity, UV absorption, polypeptide patterns, and chitin synthetase activity determinations, sediment independently of one another. An important feature was the finding that chitin synthetase from 'slime' peaked at a median specific gravity of 1.1201 +/- 0.0036, whereas that from wild-type strain sedimented at a higher buoyant density (specific g…

BiophysicsCentrifugation IsopycnicBiochemistryNeurospora crassaCell wallchemistry.chemical_compoundChitinCentrifugation Density GradientMolecular BiologyPolyacrylamide gel electrophoresisSpecific GravityDifferential centrifugationChitin SynthaseOrganellesbiologyStrain (chemistry)Neurospora crassafungiCrassaGenetic VariationSedimentationbiology.organism_classificationcarbohydrates (lipids)Molecular WeightKineticsMicroscopy ElectronNeurosporaBiochemistrychemistryGlucosyltransferasesElectrophoresis Polyacrylamide GelSpectrophotometry UltravioletBiochimica et biophysica acta
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Giant liposomes as model membranes for immunological studies: spontaneous insertion of purified K1-antigen (poly-alpha-2,8-NeuAc) of Escherichia coli.

1990

A flow chamber has been constructed to use giant liposomes (diameter 5-50 microns) as model membranes for immunological studies and other experiments involving the interaction with water-soluble compounds. As an example of immunological importance, the insertion of purified K-antigen from Escherichia coli K1 has been studied. Despite its large hydrophilic part (poly-alpha-2,8-NeuAc), which is capped at its potential reducing end with phosphatidic acid acting as a lipid anchor group, this water-soluble material is readily incorporated into liposomal membranes of dimyristoylphosphatidylcholine (DMPC). The incorporation has been proven by immunofluorescence using a FITC-labeled monoclonal anti…

BiophysicsFluorescent Antibody TechniqueNeuraminidaseBiologymedicine.disease_causeBiochemistryModels BiologicalResidue (chemistry)chemistry.chemical_compoundMembrane LipidsmedicineEscherichia coliMicroscopy Phase-ContrastEscherichia coliHEPESchemistry.chemical_classificationLiposomeAntigens BacterialAntibodies MonoclonalWaterCell BiologyPhosphatidic acidbiology.organism_classificationEnterobacteriaceaeEnzymeMembranechemistryBiochemistrySolubilityImmunoglobulin GAntigens SurfaceLiposomesDimyristoylphosphatidylcholineBiochimica et biophysica acta
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Trehalose effects on α-crystallin aggregates

2007

alpha-Crystallin in its native state is a large, heterogeneous, low-molecular weight (LMW) aggregate that under certain conditions may progressively became part of insoluble high-molecular weight (HMW) systems. These systems are supposed to play a relevant role in eye lens opacification and vision impairment. In this paper, we report the effects of trehalose on alpha-crystallin aggregates. The role of trehalose in alpha-crystallin stress tolerance, chaperone activity and thermal stability is studied. The results show that trehalose stabilizes the alpha-crystallin native structure, inhibits alpha-crystallin aggregation, and disaggregates preformed LMW systems not affecting its chaperone acti…

BiophysicsMicroscopy Atomic ForceBiochemistrythermal stabilitychemistry.chemical_compoundCrystallinNative stateThermal stabilityBenzothiazolesalpha-Crystallinsalpha-crystallinChaperone activityProtein Structure QuaternaryEye lensMolecular BiologyNative structureCircular DichroismTrehalosefood and beveragesCell BiologyTrehaloseeye diseaseschaperone activityThiazolesSpectrometry FluorescencechemistryBiochemistryaggregatesα-Crystallin Trehalose Aggregates Chaperone activity Thermal stabilitysense organsBiochemical and Biophysical Research Communications
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An enzyme caught in action: Direct imaging of hydrolytic function and domain formation of phospholipase A2 in phosphatidylcholine monolayers

1989

AbstractPhospholipase A2, a ubiquitous lipolytic enzyme that actively catalyses hydrolysis of phospholipids, has been studied as a model for enzyme-substrate reactions, as a membrane structural probe, and as a model for lipid-protein interactions. Its mechanism of action remains largely controversial. We report here for the first time direct microscopic observation of the lipolytic action of fluorescently marked phospholipase A2 (Naja naja naja) against phosphatidylcholine monolayers in the lipid phase transition region. Under these conditions, phospholipase A2 is shown to target and hydrolyse solid-phase lipid domains of L-α-dipalmitoylphosphatidylcholine. In addition, after a critical ext…

BiophysicsPhospholipid02 engineering and technologyBiochemistry03 medical and health scienceschemistry.chemical_compoundPhospholipase A2Structural BiologyPhospholipase A2PhosphatidylcholineEnzymatic hydrolysisGeneticsmedicineLipid bilayer phase behaviorMolecular BiologyDomain030304 developmental biologyFluorescence microscopy0303 health sciencesPhospholipase APhospholipase BbiologyChemistryMonolayerCell Biology021001 nanoscience & nanotechnologyPhospholipidBiochemistryMechanism of actionEnzymatic hydrolysisbiology.proteinmedicine.symptom0210 nano-technologyFEBS Letters
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Intra-operatively obtained human tissue: Protocols and techniques for the study of neural stem cells

2009

The discoveries of neural (NSCs) and brain tumor stem cells (BTSCs) in the adult human brain and in brain tumors, respectively, have led to a new era in neuroscience research. These cells represent novel approaches to studying normal phenomena such as memory and learning, as well as pathological conditions such as Parkinson's disease, stroke, and brain tumors. This new paradigm stresses the importance of understanding how these cells behave in vitro and in vivo. It also stresses the need to use human-derived tissue to study human disease because animal models may not necessarily accurately replicate the processes that occur in humans. An important, but often underused, source of human tissu…

BiopsyBrain tumorCell Culture TechniquesNerve Tissue ProteinsBiologyArticleIntraoperative PeriodIn vivoNeurosphereSpheroids CellularmedicineElectron microscopyHumansProcess (anatomy)NeuronsNeural stem cellsBrain NeoplasmsGeneral NeuroscienceStem CellsBrain tumor stem cellsHuman brainmedicine.diseaseImmunohistochemistryNeural stem cellCulture MediaMicroscopy Electronmedicine.anatomical_structureCell cultureAstrocytesNeoplastic Stem CellsTissue and Organ HarvestingNeurospheresStem cellNeuroscienceBiomarkersImmunocytochemistry
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Are IL-10+ regulatory Th17 cells implicated in the sustained response to glucocorticoid treatment in patients with giant cell arteritis? Comment on t…

2013

We have read with interest the recently published paper of Espigol-Frigole et al 1 in which the authors confirmed that interleukin (IL)-17 is highly expressed in giant cell arteritis (GCA) lesions.1–3 They also demonstrated for the first time that IL-17 expression in temporal artery biopsies (TABs) was correlated with a better outcome. Among other interesting results, the identification of Foxp3+IL-17+ T cells by confocal microscopy in TAB made the authors to hypothesize that these cells could be induced regulatory T cells (Treg) that may facilitate the remission of the disease under steroid therapy. …

BiopsyGiant Cell ArteritisImmunologyGeneral Biochemistry Genetics and Molecular Biologylaw.inventionRheumatologyRecurrenceConfocal microscopylawBiopsymedicineHumansImmunology and AllergyGlucocorticoidsmedicine.diagnostic_testbusiness.industryInterleukin-17InterleukinFOXP3Forkhead Transcription Factorsmedicine.diseaseInterleukin-10Temporal ArteriesGiant cell arteritisInterleukin 10ImmunologyTh17 CellsInterleukin 17businessGlucocorticoidmedicine.drugAnnals of the Rheumatic Diseases
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Cloning and characterization of Scavidin, a fusion protein for the targeted delivery of biotinylated molecules.

2001

We have constructed a novel fusion protein "Scavidin" consisting of the macrophage scavenger receptor class A and avidin. The Scavidin fusion protein is transported to plasma membranes where the avidin portion of the fusion protein binds biotin with high affinity and forms the basis for the targeted delivery of biotinylated molecules. Subcellular fractionation analysis, immunostaining, and electron microscopy demonstrated endosomal localization of the fusion protein. According to pulse-labeling and cross-linking studies Scavidin is found as monomers (55 kDa), dimers, and multimers, of which the 220-kDa form was the most abundant. The biotin binding capacity and active endocytosis of the bio…

Biotin bindingRecombinant Fusion ProteinsBlotting WesternGenetic VectorsPlasma protein bindingBiologyEndocytosisLigandsBiochemistrychemistry.chemical_compoundProtein structureBiotinTransduction GeneticTumor Cells CulturedAnimalsBiotinylationCloning MolecularReceptors ImmunologicMicroscopy ImmunoelectronMolecular BiologyReceptors ScavengerModels GeneticCell MembraneGene Transfer TechniquesScavenger Receptors Class ACell BiologyGliomaAvidinBlotting NorthernFusion proteinImmunohistochemistryPrecipitin TestsEndocytosisProtein Structure TertiaryRatsCross-Linking ReagentsRetroviridaeBiochemistrychemistryMicroscopy FluorescenceBiotinylationbiology.proteinDimerizationAvidinProtein BindingThe Journal of biological chemistry
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