Search results for "Biochemistry & Molecular Biology"

showing 10 items of 431 documents

Filipin labelling and intramembrane particles on the membranes of early and later autophagic vacuoles in Ehrlich ascites cells

1987

Cholesterol and intramembrane particle distribution on autophagic vacuole membranes was studied in Ehrlich ascites cells using filipin labelling and freeze-fracture electron microscopy. Unsaturated fatty acids were stained using imidazole-buffered osmium tetroxide. Autophagocytosis was induced with vinblastine, and early autophagic vacuoles were accumulated by lowering the ATP level in the cells with iodoacetate. Filipin labelling was observed in the limiting membranes of later, apparently hydrolase-containing autophagic vacuoles, whereas the most newly-formed, doublemembrane limited vacuoles were not labelled. The limiting membranes of late, residual body-type vacuoles either showed patchy…

Osmium TetroxideIodoacetatesPolyenesVacuoleBiologyVinblastineFilipinlaw.inventionMembrane LipidsMice03 medical and health scienceschemistry.chemical_compoundPhagocytosislawAutophagyAnimalsFreeze FracturingFilipinCarcinoma Ehrlich Tumor030304 developmental biology0303 health sciencesStaining and LabelingCholesterolEndoplasmic reticulum030302 biochemistry & molecular biologyAutophagyImidazolesMembrane ProteinsIntracellular MembranesCell biologyOrganoidsMicroscopy ElectronCholesterolMembranechemistryOsmium tetroxideVacuolesElectron microscopeVirchows Archiv B Cell Pathology Including Molecular Pathology
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Differential Expression of the Demosponge (Suberites domuncula) Carotenoid Oxygenases in Response to Light: Protection Mechanism Against the Self-Pro…

2012

The demosponge Suberites domuncula has been described to contain high levels of a proteinaceous toxin, Suberitine, that displays haemolytic activityIn the present study this 7–8 kDa polypeptide has been isolated and was shown to exhibit also cytotoxic effects on cells of the same species. Addition of retinal, a recently identified metabolite of β-carotene that is abundantly present in S. domuncula was found to reduce both the haemolytic and the cell toxic activity of Suberitine at a molar ratio of 1:1. Spectroscopic analyses revealed that the interaction between β-carotene and Suberitine can be ascribed to a reversible energy transfer reaction. The enzyme that synthesises retinal in the spo…

OxygenaseLightMolecular Sequence DataPharmaceutical Sciencemedicine.disease_causeretinalArticle03 medical and health sciencesSuberitineDioxygenaseβ-caroteneDrug DiscoverymedicineAnimalsAmino Acid SequenceCloning Molecularlcsh:QH301-705.5Pharmacology Toxicology and Pharmaceutics (miscellaneous)Carotenoidsponges030304 developmental biologyβ-carotene dioxygenasechemistry.chemical_classification0303 health sciencesbiologyBacteriaToxinCarotenoid oxygenase030302 biochemistry & molecular biologyProteinsSuberitine; β-carotene; retinal; β-carotene dioxygenase; sponges; <em>Suberites domuncula</em>biology.organism_classificationSuberites domunculaSuberites domunculaEnzymelcsh:Biology (General)Biochemistrychemistrybiology.proteinOxygenasesRetinaldehydeSuberitesSuberitesMarine Drugs
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Distribution and Dynamics of Transcription-Associated Proteins during Parvovirus Infection

2012

ABSTRACT Canine parvovirus (CPV) infection leads to reorganization of nuclear proteinaceous subcompartments. Our studies showed that virus infection causes a time-dependent increase in the amount of viral nonstructural protein NS1 mRNA. Fluorescence recovery after photobleaching showed that the recovery kinetics of nuclear transcription-associated proteins, TATA binding protein (TBP), transcription factor IIB (TFIIB), and poly(A) binding protein nuclear 1 (PABPN1) were different in infected and noninfected cells, pointing to virus-induced alterations in binding dynamics of these proteins.

Parvovirus CanineViral nonstructural proteinvirusesImmunologyMicrobiologyParvoviridae Infections03 medical and health sciencesVirologyAnimalsTranscription factor030304 developmental biology0303 health sciencesbiologyParvovirusBinding protein030302 biochemistry & molecular biologyCanine parvovirusFluorescence recovery after photobleachingbiology.organism_classificationMolecular biology3. Good healthVirus-Cell InteractionsCell CompartmentationInsect Sciencebiology.proteinTATA-binding proteinTranscription factor II BSubcellular FractionsTranscription Factors
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Parvovirus induced alterations in nuclear architecture and dynamics.

2009

The nucleus of interphase eukaryotic cell is a highly compartmentalized structure containing the three-dimensional network of chromatin and numerous proteinaceous subcompartments. DNA viruses induce profound changes in the intranuclear structures of their host cells. We are applying a combination of confocal imaging including photobleaching microscopy and computational methods to analyze the modifications of nuclear architecture and dynamics in parvovirus infected cells. Upon canine parvovirus infection, expansion of the viral replication compartment is accompanied by chromatin marginalization to the vicinity of the nuclear membrane. Dextran microinjection and fluorescence recovery after ph…

Parvovirus CaninevirusesGreen Fluorescent Proteinslcsh:MedicineGenome ViralKidneyParvoviridae InfectionsParvovirus03 medical and health sciencesLääketieteen bioteknologia - Medical biotechnologymedicineAnimalsHumansNuclear membraneMolecular Biology/Chromatin Structurelcsh:Science030304 developmental biologyMolecular Biology/DNA ReplicationCell Nucleus0303 health sciencesMultidisciplinaryMicroscopy ConfocalbiologyParvoviruslcsh:R030302 biochemistry & molecular biologyDNA replicationFluorescence recovery after photobleachingDextransbiology.organism_classificationMolecular biologyChromatin3. Good healthChromatinCell biologyCell nucleusmedicine.anatomical_structureViral replicationVirology/Viral Replication and Gene RegulationCatslcsh:QCell Biology/Nuclear Structure and FunctionViral genome replicationFluorescence Recovery After PhotobleachingHeLa CellsResearch ArticlePloS one
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In vivo phage display: identification of organ-specific peptides using deep sequencing and differential profiling across tissues.

2021

Abstract In vivo phage display is widely used for identification of organ- or disease-specific homing peptides. However, the current in vivo phage biopanning approaches fail to assess biodistribution of specific peptide phages across tissues during the screen, thus necessitating laborious and time-consuming post-screening validation studies on individual peptide phages. Here, we adopted bioinformatics tools used for RNA sequencing for analysis of high-throughput sequencing (HTS) data to estimate the representation of individual peptides during biopanning in vivo. The data from in vivo phage screen were analyzed using differential binding—relative representation of each peptide in the target…

Phage displayT7 phageAcademicSubjects/SCI00010virusesPeptideBiopanningComputational biologyDeep sequencing03 medical and health sciencesMiceIn vivoPeptide LibraryGeneticsAnimalsTissue DistributionMolecular Biology030304 developmental biologychemistry.chemical_classification0303 health sciencesMice Inbred BALB Cbiology030302 biochemistry & molecular biologyRNAHigh-Throughput Nucleotide Sequencingbiology.organism_classificationHigh-Throughput Screening AssayschemistryCell Surface Display TechniquesPeptidesHoming (hematopoietic)Nucleic acids research
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Therapeutic potential of alkaloids in autoimmune diseases: Promising candidates for clinical trials.

2020

Clinical investigations have characterized numerous disorders like autoimmune diseases, affecting the population at a rate of approximately 8-10%. These disorders are characterized by T-cell and auto-antibodies responses to self-molecules by immune system reactivity. Several therapeutic options have been adopted in clinics to combat such diseases, however, most of them are recurring. Thus, the discovery of new effective agents for the treatment of autoimmune diseases is paramount. In this context, natural products might be a useful alternative to the current therapies. Plant alkaloids with their substantial therapeutic history can be particularly interesting candidates for the alleviation o…

Pharmacology0303 health scienceseducation.field_of_studyPlant Alkaloidsbusiness.industry030302 biochemistry & molecular biologyPopulationContext (language use)BioinformaticsAutoimmune DiseasesClinical trial03 medical and health sciences0302 clinical medicineImmune systemAlkaloids030220 oncology & carcinogenesisMedicineAnimalsHumansbusinesseducationPhytotherapy research : PTRREFERENCES
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Pho85 and PI(4,5)P(2) regulate different lipid metabolic pathways in response to cold

2019

Lipid homeostasis allows cells to adjust membrane biophysical properties in response to changes in environmental conditions. In the yeast Saccharomyces cerevisiae, a downward shift in temperature from an optimal reduces membrane fluidity, which triggers a lipid remodeling of the plasma membrane. How changes in membrane fluidity are perceived, and how the abundance and composition of different lipid classes is properly balanced, remain largely unknown. Here, we show that the levels of phosphatidylinositol 4,5-bisphosphate [PI(4,5)P2], the most abundant plasma membrane phosphoinositide, drop rapidly in response to a downward shift in temperature. This change triggers a signaling cascade trans…

Phosphatidylinositol 45-DiphosphateSaccharomyces cerevisiae ProteinsMembrane FluiditySphingoid basesAcclimatizationOrm2PhospholipidSaccharomyces cerevisiaePhosphoinositideTriacylglycerideSphingolipidArticle03 medical and health scienceschemistry.chemical_compoundGlycogen Synthase Kinase 3Gene Expression Regulation FungalMembrane fluidityLow temperatureInositolPhosphatidylinositolProtein kinase AMolecular Biology1-IP7030304 developmental biology0303 health sciencesChemistry030302 biochemistry & molecular biologyCell MembraneCell BiologyLipid MetabolismSphingolipidCyclin-Dependent KinasesCell biologyTORC2-Pkh1-Ypk1 signaling moduleCold TemperatureCytosolMetabolic pathwayPhospholipidMetabolic Networks and PathwaysSignal Transduction
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TLR4 abrogates the Th1 immune response through IRF1 and IFN-β to prevent immunopathology during L. infantum infection

2020

A striking feature of human visceral leishmaniasis (VL) is chronic inflammation in the spleen and liver, and VL patients present increased production levels of multiple inflammatory mediators, which contribute to tissue damage and disease severity. Here, we combined an experimental model with the transcriptional profile of human VL to demonstrate that the TLR4-IFN-β pathway regulates the chronic inflammatory process and is associated with the asymptomatic form of the disease. Tlr4-deficient mice harbored fewer parasites in their spleen and liver than wild-type mice. TLR4 deficiency enhanced the Th1 immune response against the parasite, which was correlated with an increased activation of de…

PhysiologyGene ExpressionWhite Blood CellsMiceCell SignalingAnimal CellsImmune PhysiologyZoonosesImmunopathologyMedicine and Health SciencesMembrane Receptor SignalingBiology (General)Immune ResponseLeishmaniasisProtozoansLeishmaniaMice Knockout0303 health sciencesbiologyT Cells030302 biochemistry & molecular biologyEukaryotaImmune Receptor SignalingInfectious Diseasesmedicine.anatomical_structureLeishmaniasis VisceralCellular Typesmedicine.symptomLeishmania infantumResearch ArticleSignal TransductionNeglected Tropical DiseasesQH301-705.5Leishmania InfantumImmune CellsImmunologySpleenInflammationLEISHMANIOSE VISCERALMicrobiology03 medical and health sciencesImmune systemVirologyParasitic DiseasesGeneticsmedicineAnimalsMolecular Biology030304 developmental biologyInflammationProtozoan InfectionsBlood CellsOrganismsBiology and Life SciencesCell BiologyInterferon-betaTh1 CellsRC581-607Tropical Diseasesmedicine.diseasebiology.organism_classificationParasitic ProtozoansToll-Like Receptor 4IRF1Visceral leishmaniasisImmunologyTLR4ParasitologyImmunologic diseases. AllergySpleenInterferon Regulatory Factor-1
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Entry of Human Parechovirus 1

2001

ABSTRACT Human parechovirus 1 (HPEV-1) is a prototype member of parechoviruses, a recently established picornavirus genus. Although there is preliminary evidence that HPEV-1 recognizes α V integrins as cellular receptors, our understanding of early events during HPEV-1 infection is still very limited. The aim of this study was to clarify the entry mechanisms of HPEV-1, including the attachment of the virus onto the host cell surface and subsequent internalization. In blocking experiments with monoclonal antibodies against different receptor candidates, antibodies against α V and β 3 integrin subunits, in particular in combination, appeared to be the most efficient ones in preventing the HPE…

PicornavirusEndosomeImmunologyEndocytic cycleGolgi ApparatusHuman parechovirus 1EndosomesPicornaviridaePlatelet Membrane GlycoproteinsEndoplasmic ReticulumVirus ReplicationCaveolinsMicrobiologyClathrinEEA103 medical and health sciencessymbols.namesakeCapsidAntigens CDVirologyTumor Cells CulturedHumans030304 developmental biologyHost cell surface0303 health sciencesbiology030302 biochemistry & molecular biologyIntegrin beta3Clathrin-Coated VesiclesIntegrin alphaVGolgi apparatusbiology.organism_classificationVirologyClathrinEndocytosisVirus-Cell Interactions3. Good healthCell biologyInsect Sciencesymbolsbiology.proteinReceptors VirusJournal of Virology
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Structural and functional analysis of integrin alpha2I domain interaction with echovirus 1.

2004

Integrins are cell surface receptors for several microbial pathogens including echovirus 1 (EV1), a picornavirus. Cryo-electron microscopy revealed that the functional domain (alpha(2)I) of human alpha(2)beta(1) integrin binds to a surface depression on the EV1 capsid. This three-dimensional structure of EV1 bound to alpha(2)I domain provides the first structural details of an integrin interacting with a picornavirus. The model indicates that alpha(2)beta(1) integrin cannot simultaneously bind both EV1 and the physiological ligand collagen. Compared with collagen binding to the alpha(2)I domain, the virus binds with a 10-fold higher affinity but in vitro uncoating of EV1 was not observed as…

PicornavirusProtein ConformationvirusesIntegrinIntegrin alpha2EndocytosisBiochemistryCD49c03 medical and health sciencesCapsidViral entryEnterovirus InfectionsHumansMolecular Biology030304 developmental biology0303 health sciencesbiology030302 biochemistry & molecular biologyCell MembraneCryoelectron MicroscopyCell BiologyLigand (biochemistry)biology.organism_classificationMolecular biologyEnterovirus B HumanIntegrin alpha Mbiology.proteinBiophysicsMicroscopy Electron ScanningReceptors VirusIntegrin beta 6The Journal of biological chemistry
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