Search results for "Microscopy"

showing 10 items of 3390 documents

Small GTP-binding proteins of the Rho- and Ras-subfamilies are not involved in the actin rearrangements induced by attaching and effacingEscherichia …

1998

Attaching and effacing Escherichia coli (AEEC) are extracellular pathogens that induce the formation of actin-rich structures at their sites of attachment to eukaryotic host cells. We analysed whether small GTP-binding proteins of the Rho- and Ras-subfamilies, which control the cellular actin system, are essential for these bacterial-induced microfilament reorganizations. For this purpose we specifically inactivated them using the Clostridium difficile toxins TcdB-10463 and TcdB-1470. Such treatment led to a dramatic breakdown of the normal actin cytoskeleton, but did not abrogate the bacterial-induced actin rearrangements. Our data therefore indicate that the microfilament reorganizations …

Bacterial ToxinsExotoxinsArp2/3 complexmacromolecular substancesShiga ToxinsMicrofilamentMicrobiologyGTP-Binding ProteinsEscherichia coliGeneticsAnimalsHumansActin-binding proteinCytoskeletonMolecular BiologyActinbiologyClostridioides difficileActin remodelingActin cytoskeletonActinsActin CytoskeletonMicroscopy ElectronBiochemistryMicroscopy Electron Scanningras Proteinsbiology.proteinCattleMDia1HeLa CellsFEMS Microbiology Letters
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Presence of a capsule in Vibrio vulnificus biotype 2 and its relationship to virulence for eels

1993

Strains of Vibrio vulnificus biotype 2, isolated from internal organs of diseased European eels as pure cultures of opaque cells, together with some reference strains from Japanese eels, were used in this study. Spontaneous translucent-phase variants were obtained from the corresponding parent strains and compared for a variety of phenotypic traits related to virulence for eels. The rate of colony dissociation from opaque to translucent cells was higher (around 10(-2)) than that observed for translucent to opaque cells (10(-3) to 10(-4)). Electron microscopy with ruthenium red revealed the presence of a capsule of variable thickness on opaque cells, whereas translucent-type colonies had no …

Bacterial capsuleIronImmunologyVirulenceVibrio vulnificusMicrobiologyHemolysisMicrobiologyFish DiseasesVibrionaceaeAnimalsBacterial CapsulesVibrioEelsbiologyLethal doseTransferrinbiology.organism_classificationVibrioMicroscopy ElectronInfectious DiseasesVibrio InfectionsParasitologyBacterial outer membraneBacteriaBacterial Outer Membrane ProteinsPlasmidsResearch Article
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Bioencapsulation of living bacteria (Escherichia coli) with poly(silicate) after transformation with silicatein-α gene

2007

Bioencapsulation is an intriguing way to immobilize biological materials, including cells, in silica, metal-oxides or hybrid sol-gel polymers. Until now only the sol-gel precursor technology was utilized to immobilize bacteria or yeast cells in silica. With the discovery of silicatein, an enzyme from demosponges that catalyzes the formation of poly(silicate), it became possible to synthesize poly(silicate) under physiological (ambient) conditions. Here we show that Escherichia coli can be transformed with the silicatein gene, its expression level in the presence of isopropyl beta-D-thiogalactopyranoside (IPTG) can be efficiently intensified by co-incubation with silicic acid. This effect co…

Bacterial capsuleMaterials scienceBiophysicsGene Expressionlac operonBioengineeringmedicine.disease_causelaw.inventionBiomaterialschemistry.chemical_compoundlawEscherichia colimedicineTransgenesSilicic acidEscherichia coliBacterial Capsuleschemistry.chemical_classificationMicrobial ViabilitybiologySilicatesSodiumbiology.organism_classificationCathepsinsYeastEnzymechemistryBiochemistryMechanics of MaterialsMicroscopy Electron ScanningCeramics and CompositesRecombinant DNABacteriaBiomaterials
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Baculovirus entry into human hepatoma cells.

2005

ABSTRACT Autographa californica multiple nucleopolyhedrovirus (AcMNPV), a prototype member of the Baculoviridae family, has gained increasing interest as a potential vector candidate for mammalian gene delivery applications. AcMNPV is known to enter both dividing and nondividing mammalian cell lines in vitro, but the mode and kinetics of entry as well as the intracellular transport of the virus in mammalian cells is poorly understood. The general objective of this study was to characterize the entry steps of AcMNPV- and green fluorescent protein-displaying recombinant baculoviruses in human hepatoma cells. The viruses were found to bind and transduce the cell line efficiently, and electron …

BaculoviridaeCarcinoma HepatocellularEndosomeImmunoelectron microscopyvirusesImmunologyGenetic VectorsGreen Fluorescent ProteinsEndosomesBiologySpodopteraEndocytosisVirus ReplicationMicrobiologyClathrinCell Linesymbols.namesakeViral entryVirologyAnimalsHumansPinocytosisVirionGolgi apparatusbiology.organism_classificationNucleopolyhedrovirusesCell biologyVirus-Cell InteractionsInsect Sciencebiology.proteinsymbolsHepatocytesJournal of virology
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Generation of lentivirus vectors using recombinant baculoviruses

2008

In spite of advances in conventional four-plasmid transient transfection methods and development of inducible stable production cell lines, production of replication-defective lentiviral vectors in clinical scale has been challenging. Baculovirus technology offers an alternative to scalable virus production as a result of fast and easy production of baculoviruses, efficient transduction of mammalian cells and safety of the baculoviruses. As a first step toward scalable lentiviral production system, we have constructed four recombinant baculoviruses: the BAC-transfer virus expresses green fluorescent protein (GFP) as a transgene and BAC-gag-pol, BAC-vesicular stomatitis virus glycoprotein G …

BaculoviridaevirusesGenetic enhancementGenetic VectorsGreen Fluorescent ProteinsGene ExpressionVirus ReplicationCell LineGreen fluorescent proteinlaw.inventionTransduction (genetics)Transduction GeneticlawVirologyGeneticsHumansTransgenesCloning MolecularMolecular BiologyOrganisms Genetically ModifiedbiologyLentivirusGenetic TherapyFlow Cytometrybiology.organism_classificationVirologyMicroscopy FluorescenceViral replicationCell cultureLentivirusRecombinant DNAMolecular MedicineBaculoviridaeHeLa CellsGene Therapy
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Enhancing the multiplication of nucleopolyhedrovirus in vitro by manipulation of the pH

2009

Insect nucleopolyhedroviruses (NPVs) are studied widely as agents for biological control, as expression vectors for the production of heterologous proteins, and as transduction vectors for gene therapy applications. Most of these applications rely on the existence of cell lines that allow in vitro multiplication of the virus. The influence of pH in the medium culture on the multiplication of SeMNPV, HearSNPV and AcMNPV in different cell culture lines was investigated. The study showed a strong influence of the medium pH on the virus multiplication with the best results at pH 6.5, about half pH unit above the pH of insect culture media used most commonly. Additional experiments using a recom…

BaculoviridaevirusesGreen Fluorescent ProteinsCell Culture TechniquesHeterologousSpodopteraVirus ReplicationVirusCell LineGreen fluorescent proteinTransduction (genetics)VirologyAnimalsInsect virusExpression vectorbiologyfungiHydrogen-Ion ConcentrationVirus Internalizationbiology.organism_classificationMolecular biologyNucleopolyhedrovirusesCulture MediaCell biologyMicroscopy FluorescenceCell cultureJournal of Virological Methods
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Solid-State Synthesis of “Bamboo-Like” and Straight Carbon Nanotubes by Thermolysis of Hexa-peri-hexabenzocoronene–Cobalt Complexes

2006

BambooHot TemperatureTime FactorsMaterials scienceSelective chemistry of single-walled nanotubeschemistry.chemical_elementCarbon nanotubelaw.inventionBiomaterialsMicroscopy Electron TransmissionlawNanotechnologyOrganic chemistryPolycyclic CompoundsGeneral Materials ScienceArgonMethylene ChlorideNanotubes CarbonCarbon nanofiberThermal decompositionTemperatureHexa-peri-hexabenzocoroneneCobaltGeneral ChemistryMicroscopy ElectronModels ChemicalchemistryChemical engineeringMicroscopy Electron ScanningCarbon nanotube supported catalystCrystallizationCobaltBiotechnologySmall
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On-surface Synthesis of a Chiral Graphene Nanoribbon with Mixed Edge Structure.

2020

Abstract Chiral graphene nanoribbons represent an important class of graphene nanomaterials with varying combinations of armchair and zigzag edges conferring them unique structure‐dependent electronic properties. Here, we describe the on‐surface synthesis of an unprecedented cove‐edge chiral GNR with a benzo‐fused backbone on a Au(111) surface using 2,6‐dibromo‐1,5‐diphenylnaphthalene as precursor. The initial precursor self‐assembly and the formation of the chiral GNRs upon annealing are revealed, along with a relatively small electronic bandgap of approximately 1.6 eV, by scanning tunnelling microscopy and spectroscopy.

Band gapAnnealing (metallurgy)530 Physics010402 general chemistry01 natural sciencesBiochemistrygraphene nanoribbonNanomaterialslaw.inventionlawchiral edge540 Chemistrypolycyclic aromatic hydrocarbonon-surface synthesisSpectroscopyQuantum tunnelling010405 organic chemistryChemistryGraphenescanning tunneling microscopy and spectroscopyCommunicationOrganic ChemistryGeneral ChemistryCommunications0104 chemical sciencesZigzagChemical physics570 Life sciences; biologyGraphene nanoribbonsChemistry, an Asian journal
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Direct detection of repetitive, whole chromosome paint and telomere DNA probes by immunogold electron microscopy

1993

Biotinylated repetitive, whole chromosome paint and telomere DNA probes were investigated at the electron microscope level after non-isotopic in situ hybridization and direct immunogold detection. The protocol described allowed the visualization of a biotinylated chromosome 1 specific satellite DNA probe in the light microscope without silver intensification. This sensitive method was exploited to analyse factors contributing to signal strength in immunogold chromosome painting. Furthermore, it allowed us to investigate the distribution of (TTAGGG)n telomere repeats in human metaphase chromosomes and interphase nuclei. Telomeric and internal (TTAGGG)n repeats were detected at high spatial r…

Base SequenceSatellite DNAHybridization probeMolecular Sequence DataChromosomeQ-FISHImmunogold labellingTelomereBiologyMolecular biologyTelomereGeneticsBiophysicsChromosomes HumanHumansInterphaseLymphocytesDNA ProbesMicroscopy ImmunoelectronInterphaseMetaphaseIn Situ HybridizationRepetitive Sequences Nucleic AcidChromosome Research
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Characterization of cells involved in the formation of granuloma. An ultrastructural study on macrophages, epitheloid cells, and giant cells in exper…

1981

In experimental tubulo-interstitial (anti-basement membrane) nephritis of the rat, granulomatous inflammation develops around immunologically altered tubular basement membranes. The present light- and electron microscopic studies indicate that in the course of the granulomatous reaction, tissue monocytes evolve from blood monocytes and pursue two independent pathways of differentation. On the one hand they may differentiate into macrophages ("distant from tubules") or, alternatively, into epitheloid cells ("adjacent to tubules"). The latter, through cell fusion, develop into multinucleated giant cells of the Langhans' type. The cytoplasmic components of the epitheloid cells and the multinuc…

Basement membraneMaleCell fusionGranulomaInterstitial nephritisMacrophagesLanghans giant cellGeneral MedicineBiologymedicine.diseaseBasement MembraneMonocytesCell biologyRatsCell FusionMicroscopy Electronmedicine.anatomical_structureKidney TubulesGiant cellGranulomamedicineUltrastructureAnimalsNephritis InterstitialNephritisVirchows Archiv. B, Cell pathology including molecular pathology
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