Search results for "hate"

showing 10 items of 2099 documents

Mammalian BiP controls posttranslational ER translocation of the hepatitis B virus large envelope protein.

2008

AbstractThe hepatitis B virus L protein forms a dual topology in the endoplasmic reticulum (ER) via a process involving cotranslational membrane integration and subsequent posttranslational translocation of its preS subdomain. Here, we show that preS posttranslocation depends on the action of the ER chaperone BiP. To modulate the in vivo BiP activity, we designed an approach based on overexpressing its positive and negative regulators, ER-localized DnaJ-domain containing protein 4 (ERdj4) and BiP-associated protein (BAP), respectively. The feasibility of this approach was confirmed by demonstrating that BAP, but not ERdj4, destabilizes the L/BiP complex. Overexpressing BAP or ERdj4 inhibits…

Hepatitis B virusgenetic structuresBiPBiophysicsHemagglutinin (influenza)Chromosomal translocationmacromolecular substancesmedicine.disease_causeEndoplasmic ReticulumBiochemistryCell LineAdenosine TriphosphateViral Envelope ProteinsStructural BiologyIn vivoCalnexinHBVGeneticsmedicineHumansMolecular BiologyEndoplasmic Reticulum Chaperone BiPTranslocational regulationHeat-Shock ProteinsHepatitis B virusbiologyEndoplasmic reticulumMembrane ProteinsCell BiologyHSP40 Heat-Shock ProteinsMolecular biologyProtein Structure TertiaryProtein TransportDual topologyMembrane topologyProtein BiosynthesisMembrane topologybiology.proteinPosttranslational translocationMolecular ChaperonesFEBS letters
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Calorimetric investigation of the precipitation of calcium monohydrogen phosphate in water/AOT/n-heptane microemulsions

2000

Abstract The molar enthalpies of precipitation of calcium monohydrogen phosphate (CaHPO 4 ) in water/sodium bis(2-ethylhexyl) sulfosuccinate (AOT)/ n -heptane microemulsions were measured at 25°C by a calorimetric technique as a function of the molar ratio R ( R  = [water]/[AOT]) at a fixed AOT concentration. Calorimetric data indicate the formation of CaHPO 4 nanoparticles encapsulated in the aqueous core of the AOT reversed micelles displaying a slow growing process with time. Their energetic state is initially different from that in bulk water approaching the value in water at longer times. The observed growing process results to be completely inhibited by the presence of small amounts o…

HeptaneAqueous solutionSodiumInorganic chemistrychemistry.chemical_elementCondensed Matter PhysicsPhosphateMicellechemistry.chemical_compoundchemistryPulmonary surfactantMonolayerMicroemulsionPhysical and Theoretical ChemistryInstrumentationThermochimica Acta
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6-Phosphofructokinase from frog skeletal muscle: purification and properties

1990

HexosediphosphatesMusclesPhosphofructokinase-1Rana temporariaFrog skeletal muscleBiochemistryCitric AcidEnzyme ActivationKineticsEnzyme activatorchemistry.chemical_compoundAdenosine TriphosphatechemistryBiochemistryAnimalsCitratesPhosphofructokinase 1HexosediphosphatesCitric acidAdenosine triphosphatePhosphofructokinaseBiochemical Society Transactions
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Osmotic conditions in rheologic properties of erytrocites

2001

Abstract The decreasing viability and in vivo survival of red blood cells, RBCs, observed in blood bank-storage are due to alterations in their rheologic properties and metabolic status. However, there is a lack of electrokinetic experiments with erythrocytes by the screening produced by the high concentration of buffer required to keep the isoosmotic conditions. Electrokinetic measurements in a wide range of sodium chloride and tetrasodium pyrophosphate are undertaken on liposomes as cell models, and in order to get an aqueous media suitable for maintaining osmotic conditions and allowing electrophoretic mobility measurements as well, advantage has been taken of dextrose properties. Measur…

High concentrationchemistry.chemical_compoundElectrophoresisLiposomeElectrokinetic phenomenaColloid and Surface ChemistryChromatographychemistryAqueous mediumSodiumchemistry.chemical_elementTetrasodium pyrophosphateColloids and Surfaces A: Physicochemical and Engineering Aspects
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Biomimetic routes to micro/nanofabrication

2020

Abstract The discovery of inorganic polyphosphate (polyP), an evolutionarily ancient biopolymer, and of its function in energy storage/supply and induction of cell differentiation through specific gene expression (“morphogenetic activity”) has opened new opportunities in regenerative medicine, including therapy of bone, cartilage, and vascular diseases. Inspired by nature, various procedures have been developed for the preparation of amorphous nano and microparticles of polyP with different counterions, which mimic the physiological polyP found in blood platelets/acidocalcisomes, as well as for the preparation of morphogenetically active polyP coacervate complexes. This chapter summarizes t…

High energychemistry.chemical_compoundCoacervateNanolithographychemistryPolyphosphateNano-technology industry and agricultureengineeringNanotechnologyBiopolymerengineering.materialRegenerative medicine
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Breakdown of high-energy phosphate compounds and lactate accumulation during short supramaximal exercise.

1987

Muscle ATP, creatine phosphate and lactate, and blood pH and lactate were measured in 7 male sprinters before and after running 40, 60, 80 and 100 m at maximal speed. The sprinters were divided into two groups, group 1 being sprinters who achieved a higher maximal speed (10.07 +/- 0.13 m X s-1) than group 2 (9.75 +/- 0.10 m X s-1), and who also maintained the speed for a longer time. The breakdown of high-energy phosphate stores was significantly greater for group 1 than for group 2 for all distances other than 100 m; the breakdown of creatine phosphate for group 1 was almost the same for 40 m as for 100 m. Muscle and blood lactate began to accumulate during the 40 m exercise. The accumulat…

High-energy phosphateAdultMalePhosphocreatinePhysiologyPhysical ExertionPhysical exerciseCreatinePhosphocreatinePhosphatesRunning03 medical and health scienceschemistry.chemical_compound0302 clinical medicineAnimal scienceAdenosine TriphosphatePhysiology (medical)HumansOrthopedics and Sports MedicineGlycolysisMusclesPublic Health Environmental and Occupational Health030229 sport sciencesGeneral MedicineMetabolismHydrogen-Ion ConcentrationPhosphatechemistryBiochemistryLactatesMaximal exerciseEnergy MetabolismGlycolysis030217 neurology & neurosurgeryEuropean journal of applied physiology and occupational physiology
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Châteaux de Bourgogne

2015

International audience

HistoireChateauxMoyen Âge[SHS.ARCHEO] Humanities and Social Sciences/Archaeology and Prehistory[SHS.ARCHEO]Humanities and Social Sciences/Archaeology and PrehistoryArchéologie[ SHS.ARCHEO ] Humanities and Social Sciences/Archaeology and PrehistoryBourgogneComputingMilieux_MISCELLANEOUS
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Autophagy, cathepsin L transport, and acidification in cultured rat fibroblasts.

1992

The mechanisms of enzyme delivery to and acidification of early autophagic vacuoles in cultured fibroblasts were elucidated by cryoimmunoelectron microscopic methods. The cation-independent mannose-6-phosphate receptor (MPR) was used as a marker of the pre-lysosomal compartment, and cathepsin L and an acidotropic amine (3-(2,4-dinitroanilino)-3'-amino-N-methyl-dipropylamine (DAMP), a cytochemical probe for low-pH organelles) as markers of both pre-lysosomal and lysosomal compartments. In addition, cationized ferritin was used as an endocytic marker. In ultrastructural double labeling experiments, the bulk of all the antigens was found in vesicles containing tightly packed membrane material…

HistologyCathepsin LEndocytic cycleFluorescent Antibody TechniqueReceptors Cell SurfaceVacuoleReceptor IGF Type 2Cathepsin LEndopeptidasesOrganelleAutophagyAnimalsMicroscopy ImmunoelectronCells CulturedCathepsinMannosephosphatesbiologyVesicleBiological TransportFibroblastsHydrogen-Ion ConcentrationCathepsinsRatsCell biologyFerritinCysteine EndopeptidasesDinitrobenzenesBiochemistryCytoplasmbiology.proteinAnatomyJournal of Histochemistry & Cytochemistry
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A cytochemical study on the effects of energy deprivation on autophagocytosis in Ehrlich ascites tumor cells

1988

The effect of energy deprivation on autophagocytosis in Ehrlich ascites tumor cells was studied using cytochemical techniques. Autophagocytosis was induced with vinblastine incubation (0.1 mM) and the cellular ATP-level was lowered with 2-deoxy-D-glucose (0.35 mM). Acid phosphatase was used as a marker for lysosomal enzymes and imidazole-buffered osmium tetroxide impregnation in order to study the effects of energy deprivation on the maturation of autophagic vacuole (AV) membranes. Control and vinblastine treated cells maintained their ATP-levels throughout the incubation period tested (120 min). 2-Deoxy-D-glucose alone and with vinblastine decreased the intracellular ATP-level significantl…

HistologyPhagocytosisAcid PhosphataseVacuoleDeoxyglucoseBiologyMicechemistry.chemical_compoundAdenosine TriphosphatePhagocytosisDeoxy SugarsAutophagymedicineAnimalsCarcinoma Ehrlich TumorMolecular Biologychemistry.chemical_classificationAcid phosphataseCell BiologyGeneral MedicineVinblastineMicroscopy ElectronMedical Laboratory TechnologyEnzymeBiochemistryOsmium tetroxidechemistryCell cultureCytochemistrybiology.proteinAnatomyGeneral Agricultural and Biological Sciencesmedicine.drugHistochemistry
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In vivo detection of cytokeratin filament network breakdown in cells treated with the phosphatase inhibitor okadaic acid.

2001

We have previously described vulva carcinoma-derived A-431 subclone AK13-1, which stably expresses fluorescently labeled cytokeratin filaments (CKFs). Time-lapse fluorescence microscopy of these cells permits the continuous monitoring of the dynamics of the CKF cytoskeleton in vivo. To study mechanisms and principles of CKF disassembly as it occurs, e.g., during mitosis and liver disease, we have treated cells with the phosphatase inhibitor okadaic acid (OA), which induces complete CKF network breakdown within 3–5 h without significantly affecting the organization of the actin- and tubulin-based cytofilaments. In time-lapse movies, we find that the network breakdown starts at the cell perip…

HistologyTime FactorsRecombinant Fusion ProteinsGreen Fluorescent ProteinsPathology and Forensic Medicinechemistry.chemical_compoundCytokeratinAdenosine TriphosphateStress FibersOkadaic AcidFluorescence microscopeTumor Cells CulturedHumansEnzyme InhibitorsPhosphorylationCytoskeletonMitosisActinCytoskeletonbiologyVulvar NeoplasmsEpithelial CellsCell BiologyOkadaic acidCell biologyCytoskeletal ProteinsLuminescent ProteinsTubulinchemistryDesmoplakinsMicroscopy FluorescenceCytoplasmbiology.proteinKeratinsFemaleIndicators and ReagentsCell and tissue research
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