Search results for "Teas"

showing 10 items of 619 documents

ID: 37

2015

During the early phase of human cytomegalovirus (HCMV) infection, the Interferon- γ -Inducible factor 16 (IFI16) behaves as a pattern recognition receptor (PRR) sensing viral DNA and triggering antiviral cytokine release. Later on, it restricts virus replication by down-regulating expression of viral genes committed to DNA synthesis including UL54 and UL44. These activities are modulated by viral proteins including pUL83, a tegument protein involved in viral evasion. Here, we demonstrate that pUL83 interacts with IFI16 relieving its inhibitory activity on UL54 gene transcription. We also establish that, starting from 48 h post-infection, IFI16 is stabilized and protected from degradation by…

Human cytomegalovirusDNA synthesisIFI16virusesImmunologyMutantHematologyBiologymedicine.diseaseBiochemistryMolecular biologyViral replicationInterferonGene expressionmedicineProteasome inhibitorImmunology and AllergyMolecular Biologymedicine.drugCytokine
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Cryptogein-Induced Anion Effluxes

2014

Anion effluxes are amongst the earliest reactions of plant cells to elicitors of defence responses. However, their properties and their role in disease resistance remain almost unknown. We previously demonstrated that cryptogein, an elicitor of tobacco defence responses, induces a nitrate (NO(3) (-)) efflux. This efflux is an early prerequisite to the cryptogein-triggered hypersensitive response (HR). Here, we analyzed the electrophysiological properties of the elicitor-mediated NO(3) (-) efflux and clarified the mechanisms through which it contributes to cell death. Application of the discontinuous single electrode voltage-clamp technique in tobacco cells elicited with cryptogein enabled u…

Hypersensitive responseProgrammed cell death[SDV]Life Sciences [q-bio]chemistry.chemical_elementPlant ScienceBiologyCalciumCELL DEATHCALCIUM[SDV.GEN.GPL]Life Sciences [q-bio]/Genetics/Plants genetics[SDV.GEN.GPL] Life Sciences [q-bio]/Genetics/Plants genetics[SDV.BV]Life Sciences [q-bio]/Vegetal BiologyPLASMA MEMBRANE DEPOLARIZATIONComputingMilieux_MISCELLANEOUSCRYPTOGEINfood and beveragesDepolarizationPlant cell[SDV.BV.PEP]Life Sciences [q-bio]/Vegetal Biology/Phytopathology and phytopharmacyElicitorCell biologyPROTEASESElectrophysiologychemistryBiochemistryEffluxResearch PaperANION CHANNELSPlant Signaling & Behavior
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Cryptogein affects expression of alpha3, alpha6 and beta1 20S proteasome subunits encoding genes in tobacco.

2001

Twelve a and b 20S proteasome subunits cDNAs showing 70–82% identity with the corresponding genes in Arabidopsis or rice, and features of eukaryotic proteasome subunits were cloned in tobacco. Only b1-tcI 7, a3 and a6, 20S proteasome subunits encoding genes were up-regulated by cryptogein, a proteinaceous elicitor of plant defence reactions. These results led to the hypothesis that the activation of b1-tcI 7, a3 and a6 could induce a specific proteolysis involved in the hypersensitive response and systemic acquired resistance monitored by cryptogein. In eukaryotes, the 26S proteasome is the central multicatalytic proteinase complex comprising two subcomplexes: the 20S core particle that per…

Hypersensitive responseProteasome Endopeptidase ComplexPhysiologyProtein subunitProteolysisMolecular Sequence DataPlant ScienceGenes PlantGene Expression Regulation EnzymologicFungal ProteinsGene Expression Regulation PlantMultienzyme ComplexesArabidopsisGene expressionTobaccomedicineAmino Acid SequenceGenePlant Diseasesbiologymedicine.diagnostic_testAlgal Proteinsbiology.organism_classificationPlants Genetically ModifiedCysteine EndopeptidasesProteasomeBiochemistryProtein foldingJournal of experimental botany
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Characterization of a new, nonpathogenic mutant of Botrytis cinerea with impaired plant colonization capacity.

2006

International audience; Botrytis cinerea is a necrotrophic pathogen that attacks more than 200 plant species.Here, the nonpathogenic mutant A336, obtained via insertional mutagenesis, was characterized.Mutant A336 was nonpathogenic on leaves and fruits, on intact and wounded tissue, while still able to penetrate the host plant. It grew normally in vitro on rich media but its conidiation pattern was altered. The mutant did not produce oxalic acid and exhibited a modified regulation of the production of some secreted proteins (acid protease 1 and endopolygalacturonase 1). Culture filtrates of the mutant triggered an important oxidative burst in grapevine ( Vitis vinifera ) suspension cells, a…

Hypersensitive responsehypersensitive responsePhysiology[SDV]Life Sciences [q-bio]colonisationMutantArabidopsisConidiationPlant ScienceMicrobiologyInsertional mutagenesisFungal Proteins03 medical and health sciencesPlasmidGene Expression Regulation FungalOnionsBotrytis cinerea; endopolygalacturonase BcPG1; hypersensitive responseVitismutantoxidative burstPathogenGene030304 developmental biologyBotrytis cinereaPhaseolus0303 health sciencesoxalateendopolygalacturonase BcPG1biology030306 microbiologyOxalic Acidfungifood and beveragesHydrogen-Ion Concentrationbiology.organism_classificationImmunity Innatenonpathogenic mutantEnzymesPlant LeavesMutagenesis Insertionalnonaspartyl acid protease ACP1Mutationbotrytis cinerea;endopolygalacturonase BcPG1;hypersensitive response;nonaspartyl acid protease ACP1;nonpathogenic mutant;oxalate;oxidative burstBotrytisbotrytis cinereaReactive Oxygen SpeciesThe New phytologist
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Rapid inactivation and proteasome-mediated degradation of OGG1 contribute to the synergistic effect of hyperthermia on genotoxic treatments

2013

Inhibition of DNA repair has been proposed as a mechanism underlying heat-induced sensitization of tumour cells to some anticancer treatments. Base excision repair (BER) constitutes the main pathway for the repair of DNA lesions induced by oxidizing or alkylating agents. Here, we report that mild hyperthermia, without toxic consequences per se, affects cellular DNA glycosylase activities, thus impairing BER. Exposure of cells to mild hyperthermia leads to a rapid and selective inactivation of OGG1 (8-oxoguanine DNA glycosylase) associated with the relocalisation of the protein into a detergent-resistant cellular fraction. Following its inactivation, OGG1 is ubiquitinated and directed to pro…

HyperthermiaProteasome Endopeptidase ComplexPyrrolidinesDNA RepairDNA repairUbiquitin-Protein Ligases[SDV.BC.BC]Life Sciences [q-bio]/Cellular Biology/Subcellular Processes [q-bio.SC]BiochemistryDNA Glycosylases03 medical and health scienceschemistry.chemical_compound0302 clinical medicineUbiquitinEnzyme StabilitymedicineHumans[SDV.BBM.BC]Life Sciences [q-bio]/Biochemistry Molecular Biology/Biochemistry [q-bio.BM]Molecular BiologyComputingMilieux_MISCELLANEOUSCell Proliferation030304 developmental biologyCell Nucleus0303 health sciencesPhotosensitizing AgentsbiologyCell growthUbiquitinationCell BiologyBase excision repairmedicine.diseaseMolecular biology[SDV.BBM.BC]Life Sciences [q-bio]/Biochemistry Molecular Biology/Biomolecules [q-bio.BM]Protein TransportProteasomechemistryDNA glycosylase030220 oncology & carcinogenesisProteolysisCancer researchbiology.proteinHeat-Shock ResponseQuinolizinesDNADNA DamageHeLa Cells
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Salivary protein profiles and sensitivity to the bitter taste of caffeine.

2011

WOS: 000298381900008; International audience; The interindividual variation in the sensitivity to bitterness is attributed in part to genetic polymorphism at the taste receptor level, but other factors, such as saliva composition, might be involved. In order to investigate this, 2 groups of subjects (hyposensitive, hypersensitive) were selected from 29 healthy male volunteers based on their detection thresholds for caffeine, and their salivary proteome composition was compared. Abundance of 26 of the 255 spots detected on saliva electrophoretic patterns was significantly different between hypo- and hypersensitive subjects. Saliva of hypersensitive subjects contained higher levels of amylase…

Immunoglobulin AMaleSalivaPhysiologymedicine.medical_treatment[ SDV.AEN ] Life Sciences [q-bio]/Food and Nutritionperceptionbitternessin-vivoBehavioral Neurosciencechemistry.chemical_compound0302 clinical medicineTaste receptorphenolic astringent stimuliAmylase0303 health scienceswhole salivabiologyperiodontitis patientsMiddle AgedSensory Systemsmucosal pellicleTasteTaste ThresholdCystatinCaffeineimmunoglobulin-acystatinsAdultmedicine.medical_specialtyproteolysisproteomeSerum albumin03 medical and health sciencesstomatognathic systemPhysiology (medical)Internal medicineCaffeinemedicineHumansSalivary Proteins and Peptidescystatin030304 developmental biologysalivaProteasealpha-amylase030206 dentistryEndocrinologychemistrytwo-dimensionalelectrophoresisbiology.protein[SDV.AEN]Life Sciences [q-bio]/Food and Nutritionhealthy-subjects
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Secreted proteophosphoglycan of Leishmania mexicana amastigotes activates complement by triggering the mannan binding lectin pathway.

1997

Cutaneous lesions induced by infection of mice with the protozoan parasite, Leishmania mexicana, contain abundant amounts of a high molecular mass proteophosphoglycan (PPG), which is secreted by the amastigote stage residing in phagolysosomes of macrophages and can then be released into the tissue upon rupture of the infected cells. Amastigote PPG forms sausage-shaped but soluble particles and belongs to a novel class of serine-rich proteins that are extensively O-glycosylated by phosphooligosaccharides capped by mannooligosaccharides. The purified molecule is shown here to efficiently activate complement (C) and deplete hemolytic activity of normal serum and may prevent the opsonization of…

ImmunologyLeishmania mexicanaProtozoan ProteinsCollectinLeishmaniasis CutaneousLeishmania mexicanaMiceImmunology and AllergyAnimalsAmastigoteComplement ActivationMannan-binding lectinSerine proteaseMice KnockoutbiologyMacrophagesComplement C4Complement C3biology.organism_classificationCollectinsComplement systemAntibody opsonizationBiochemistryLectin pathwaybiology.proteinMice Inbred CBACalciumProteoglycansCarrier ProteinsEuropean journal of immunology
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Persistent and Transient Replication of Full-Length Hepatitis C Virus Genomes in Cell Culture

2002

ABSTRACT The recently developed subgenomic hepatitis C virus (HCV) replicons were limited by the fact that the sequence encoding the structural proteins was missing. Therefore, important information about a possible influence of these proteins on replication and pathogenesis and about the mechanism of virus formation could not be obtained. Taking advantage of three cell culture-adaptive mutations that enhance RNA replication synergistically, we generated selectable full-length HCV genomes that amplify to high levels in the human hepatoma cell line Huh-7 and can be stably propagated for more than 6 months. The structural proteins are efficiently expressed, with the viral glycoproteins E1 and…

ImmunologyReplicationGenome ViralHepacivirusBiologyVirus ReplicationMicrobiologyVirusViral ProteinsGene FrequencyVirologyTumor Cells CulturedHumansSubgenomic mRNAchemistry.chemical_classificationEndoplasmic reticulumRNAHepatitis CMolecular biologyNS2-3 proteasechemistryViral replicationCell cultureCulture Media ConditionedInsect ScienceRNA ViralGlycoproteinSubcellular FractionsJournal of Virology
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Exploring the non-covalent ligand-binding mechanism on immunoproteasome by enhanced Molecular Dynamics

2021

Selective inhibition of immunoproteasome is a valuable strategy to treat autoimmune and inflammatory diseases, and hematologic malignancies. In particular, non-covalent inhibition is strongly desirable because it is free of the drawbacks and side effects associated with covalent inhibition. Recently, a new series of amide derivatives with Ki values in the low/submicromolar ranges toward the β1i subunit have been identified as non-covalent inhibitors 1 . We investigated the binding mechanism of the most potent and selective inhibitor (1) to elucidate the steps from the ligand entrance into the binding pocket to the ligand-induced conformational changes. We carried out a total of 400ns of MD-…

Immunoproteasome non-covalent inhibitors enhanced molecular dynamics
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Ultrastructure of the Interlamellar Membranes of the Nacre of the Bivalve Pteria hirundo, Determined by Immunolabelling.

2015

The current model for the ultrastructure of the interlamellar membranes of molluscan nacre imply that they consist of a core of aligned chitin fibers surrounded on both sides by acidic proteins. This model was based on observations taken on previously demineralized shells, where the original structure had disappeared. Despite other earlier claims, no direct observations exist in which the different components can be unequivocally discriminated. We have applied different labeling protocols on non-demineralized nacreous shells of the bivalve Pteria. With this method, we have revealed the disposition and nature of the different fibers of the interlamellar membranes that can be observed on the …

In situPlateletsBivalvesScanning electron microscopeShell (structure)Mineralogylcsh:MedicineChitinMatrix (biology)chemistry.chemical_compoundChitinAnimal ShellsMembrane proteinsAnimalsFiberlcsh:ScienceNacreFluorescence microscopyMultidisciplinaryMicroscopy Confocallcsh:RfungiProteasesMolluscs[ SDV.IB.BIO ] Life Sciences [q-bio]/Bioengineering/BiomaterialsBivalviaMembraneAragonitechemistryBiophysicsUltrastructureMicroscopy Electron Scanninglcsh:QResearch ArticlePloS one
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