Search results for "Peptide fragment"

showing 10 items of 356 documents

A nonsense mutation abrogates production of a functional enterotoxin A in Clostridium difficile toxinotype VIII strains of serogroups F and X.

1999

Clostridium difficile strains of toxinotype VIII from serogroups F and X are described as toxin B-positive, toxin A-negative (TcdB+ A-), although they harbour almost the entire tcdA gene. To identify the reason for the lack of TcdA detection, we analyzed catalytic and ligand domains of TcdA-1470 of the type strain of serogroup F, strain 1470. Using recombinant fragments, the C-terminal immunodominant ligand domain TcdA3-1470, spanning amino acid residues 1694-2711 (corresponding to VPI 10463 sequence), was detected in Western blots. Similar experiments using the recombinant N-terminal catalytic fragment TcdAc1-2-1470 (amino acid positions 1-544) failed. In addition, this fragment showed no …

Nonsense mutationBlotting WesternMutation MissenseEnterotoxinBiologymedicine.disease_causeMicrobiologyMicrobiologylaw.inventionEnterotoxinsBacterial ProteinslawCatalytic DomainGeneticsmedicineMissense mutationHumansMolecular BiologyGenechemistry.chemical_classificationMutationClostridioides difficileMolecular biologyStop codonPeptide FragmentsRecombinant ProteinsAmino acidchemistryGenes BacterialRecombinant DNAGene DeletionFEMS microbiology letters
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NATURAL SELECTION AND THE ORGAN-SPECIFIC DIFFERENTIATION OF HIV-1 V3 HYPERVARIABLE REGION

2004

The existence of organ-specific HIV-1 populations within infected hosts has been studied for many years; nonetheless results reported by different authors are somewhat discrepant. To tackle this problem, we used a population genetics approach to analyze previously published data from the V3 hypervariable region of the envelope env gene. Our results are compatible with a population subdivision by organs in 95% of individuals analyzed at autopsy. In addition, populations infecting the nervous system and testicles clearly appear as differentiated subsets of the so-called macrophage-tropic variants. Liver and kidney may harbor differentiated populations as well. Although it is widely accepted t…

Nonsynonymous substitutionPopulationPopulation geneticsHIV Envelope Protein gp120BiologyEvolution MolecularGeneticsCluster AnalysisHumansSelection GeneticeducationEcology Evolution Behavior and SystematicsGeneticsAnalysis of VarianceLikelihood Functionseducation.field_of_studyNatural selectionBase SequenceModels GeneticMechanism (biology)HIVPeptide FragmentsHypervariable regionGenetics PopulationOrgan SpecificityViral evolutionAdaptationDatabases Nucleic AcidGeneral Agricultural and Biological SciencesSequence AlignmentEvolution
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In-depth evaluation of software tools for data-independent acquisition based label-free quantification.

2015

Label-free quantification (LFQ) based on data-independent acquisition workflows currently experiences increasing popularity. Several software tools have been recently published or are commercially available. The present study focuses on the evaluation of three different software packages (Progenesis, synapter, and ISOQuant) supporting ion mobility enhanced data-independent acquisition data. In order to benchmark the LFQ performance of the different tools, we generated two hybrid proteome samples of defined quantitative composition containing tryptically digested proteomes of three different species (mouse, yeast, Escherichia coli). This model dataset simulates complex biological samples con…

Normalization (statistics)ProteomicsProteomeComputer sciencebusiness.industrycomputer.software_genreBiochemistryMass SpectrometryPeptide FragmentsIdentifierLabel-free quantificationSoftwareIsoquantYeastsProteomeEscherichia coliHumansData-independent acquisitionData miningCluster analysisbusinessMolecular BiologycomputerSoftwareProteomics
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Gliadin activates arginase pathway in RAW264.7 cells and in human monocytes

2014

AbstractCeliac disease (CD) is an autoimmune enteropathy triggered in susceptible individuals by the ingestion of gliadin-containing grains. Recent studies have demonstrated that macrophages play a key role in the pathogenesis of CD through the release of inflammatory mediators such as cytokines and nitric oxide (NO). Since arginine is the obliged substrate of iNOS (inducible nitric oxide synthase), the enzyme that produces large amount of NO, the aim of this work is to investigate arginine metabolic pathways in RAW264.7 murine macrophages after treatment with PT-gliadin (PTG) in the absence and in the presence of IFNγ. Our results demonstrate that, besides strengthening the IFNγ-dependent …

OrnithineArginineBlotting WesternNitric Oxide Synthase Type IIOrnithine DecarboxylaseReal-Time Polymerase Chain ReactionArginineMonocytesGliadinOrnithine decarboxylaseInterferon-gammaMicechemistry.chemical_compoundmedicineAnimalsHumansCeliac diseaseMacrophageRNA MessengerMolecular BiologyCells CulturedArginasebiologyReverse Transcriptase Polymerase Chain ReactionMacrophagesMonocytenutritional and metabolic diseasesNitric oxideOrnithineMolecular biologyPeptide FragmentsNitric oxide synthaseArginasemedicine.anatomical_structureBiochemistrychemistrybiology.proteinMolecular MedicineInterferon-γGliadinBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
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Modification of the proteolytic fragmentation pattern upon oxidation of cysteines from ribulose 1,5-bisphosphate carboxylase/oxygenase.

2003

The proteolytic susceptibility of the native CO 2 -fixing photosynthetic enzyme ribulose 1,5-bisphosphate carboxylase/oxygenase (EC 4.1.1.39, Rubisco) has been shown to increase in vitro after oxidative treatments that affect cysteine thiols. A limited incubation of oxidized (pretreated with the disulfide cystamine) Rubisco from Chlamydomonas reinhardtii with subtilisin or proteinase K generated fragments of molecular mass about 53 kDa (band I in SDS-PAGE) and 47 kDa (band II) derived from the large subunit (55 kDa) of the enzyme. In contrast, proteolysis of the reduced Rubisco (pretreated with the free thiol cysteamine) produced only the 53 kDa band. The same fragmentation pattern was repr…

OxygenaseProtein subunitRibulose-Bisphosphate CarboxylaseMolecular Sequence DataBiochemistrychemistry.chemical_compoundEndopeptidasesAnimalsEuglena gracilisAmino Acid SequenceCysteineConserved SequenceRibulose 15-bisphosphatebiologyRibuloseHydrolysisfungiRuBisCOSubtilisinPeptide FragmentsKineticsProtein SubunitschemistryBiochemistryModels Chemicalbiology.proteinProtein quaternary structureHoloenzymesOxidation-ReductionProtein Processing Post-TranslationalChlamydomonas reinhardtiiCysteineBiochemistry
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Protection of Flupirtine on β-Amyloid-Induced Apoptosis in Neuronal Cells In Vitro: Prevention of Amyloid-Induced Glutathione Depletion

2002

Effective drugs are not available to protect against beta-amyloid peptide (A beta)-induced neurotoxicity. Cortical neurons from rat embryos were treated with the toxic fragment A beta25-35 at 1 microM in the presence or absence of flupirtine, a triaminopyridine, successfully applied clinically as a nonopiate analgesic drug. Five days later 1 microM A beta25-35 caused reduction of cell viability to 31.1%. Preincubation of cells with flupirtine (1 or 5 microg/ml) resulted in a significant increase of the percentage of viable cells (74.6 and 65.4%, respectively). During incubation with A beta25-35 the neurons undergo apoptosis as determined by appearance of the characteristic stepladder-like D…

Pathologymedicine.medical_specialtyCell SurvivalAminopyridinesApoptosisPharmacologymedicine.disease_causeBiochemistryAntioxidantsCellular and Molecular NeurosciencemedicineAnimalsViability assaySenile plaquesRats WistarCerebral CortexNeuronsAmyloid beta-PeptidesChemistryNeurotoxicitymedicine.diseaseGlutathionePeptide FragmentsRatsOxidative StressNeuroprotective AgentsApoptosisCell cultureDNA fragmentationFlupirtineOxidative stressmedicine.drugJournal of Neurochemistry
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Comparison of monolithic and microparticulate columns for reversed-phase liquid chromatography of tryptic digests of industrial enzymes in cleaning p…

2011

Abstract Enzymes of several classes used in the formulations of cleaning products were characterized by trypsin digestion followed by HPLC with UV detection. A polymeric monolithic column (ProSwift) was used to optimize the separation of both the intact enzymes and their tryptic digests. This column was adequate for the quality control of raw industrial enzyme concentrates. Then, monolithic and microparticulate columns were compared for peptide analysis. Under optimized conditions, the analysis of tryptic digests of enzymes of different classes commonly used in the formulation of cleaning products was carried out. Number of peaks, peak capacity and global resolution were obtained in order t…

Peptide analysisChromatography Reverse-PhaseMonolithic HPLC columnChromatographyResolution (mass spectrometry)ChemistryOrganic ChemistryDetergentsReproducibility of ResultsGeneral MedicineReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyPeptide FragmentsAnalytical ChemistryEnzymesIndustrial enzymesTrypsinTrypsin DigestionUv detectionJournal of chromatography. A
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Mumijo traditional medicine: fossil deposits from Antarctica (chemical composition and beneficial bioactivity)

2008

Mumijo is a widely used traditional medicine, especially in Russia, Altai Mountains, Mongolia, Iran Kasachstan and in Kirgistan. Mumijo preparations have been successfully used for the prevention and treatment of infectious diseases; they display immune-stimulating and antiallergic activity as well. In the present study, we investigate the chemical composition and the biomedical potential of a Mumijo(-related) product collected from the Antarctica. The yellow material originates from the snow petrels,Pagodroma nivea. Extensive purification and chemical analysis revealed that the fossil samples are a mixture of glycerol derivatives.In vitroexperiments showed that the Mumijo extract caused in…

Peptide fragmentSUBSTANCESBiologyWAX ESTERSchemistry.chemical_compoundSTOMACH OIL DEPOSITSGLYCERYL ETHERSGlycerolGlycerol EthersPETRELSChemical compositionSUSTAINABLE EXPLOITATIONWaxTraditional medicineCortical neuronslcsh:Other systems of medicineIN-VITROlcsh:RZ201-999DIFFERENTIATIONComplementary and alternative medicinechemistryvisual_artCELLSvisual_art.visual_art_mediumOriginal ArticleGlycerol DerivativesALKOXYGLYCEROLS
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PRK1 phosphorylates MARCKS at the PKC sites: serine 152, serine 156 and serine 163

1996

AbstractThe 80kDa Myristolated Alanine-Rich C-Kinase Substrate (MARCKS) in a major in vivo substrate of protein kinase C (PKC). Here we report that MARCKS is a major substrate for the lipid-activated PKC-related kinase (PRK1) in cell extracts. Furthermore, PRK1 is shown to phosphorylate MARCKS on the same sites as PKC in vitro. Thus, control of MARCKS phosphorylation on these previously identified ‘PKC’ sites may be regulated under certain circumstances by PRK as well as PKC mediated signalling pathways. The implications for MARCKS as a marker of PKC activation and as a point of signal convergence are discussed.

PhosphopeptidesMARCKSPRKRecombinant Fusion ProteinsMolecular Sequence DataBiophysicsKidneyBiochemistryCell-free systemCell LineSerineStructural BiologyProtein kinase CGeneticsAnimalsAmino Acid SequenceBinding siteMARCKSPKCPhosphorylationMyristoylated Alanine-Rich C Kinase SubstrateMolecular BiologyProtein kinase CGlutathione TransferaseBinding SitesCell-Free SystemKinaseChemistryIntracellular Signaling Peptides and ProteinsMembrane ProteinsProteinsCell BiologyHaplorhiniPeptide FragmentsBiochemistryPhosphorylationElectrophoresis Polyacrylamide GelSignal transductionSequence AnalysisSignal TransductionFEBS Letters
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Milk versus caseinophosphopeptides added to fruit beverage: Resistance and release from simulated gastrointestinal digestion

2010

The influence of simulated gastrointestinal digestion on caseinophosphopeptides (CPPs) formation in milk-based fruit beverage was evaluated, together with resistance of a pool of CPPs added to fruit beverage. In milk-based fruit beverage, four CPPs were identified that can be justified by their presence in raw milk or due to processing. When it was subjected to simulated gastrointestinal digestion, 10 CPPs were identified, and only 1 presented the cluster (SpSpSpEE) (3 phosphoseryl group followed by 2 glutamic acid residues), which corresponded to αs2-CN(1-19)4P. CPPs added to fruit beverage are resistant to simulated gastrointestinal digestion, and 16 CPPs were identified originating from …

PhosphopeptidesPhysiologyChemistryFruit drinksMolecular Sequence DataCaseinsfood and beveragesRaw milkBiochemistryPeptide FragmentsGastrointestinal digestionBeveragesGastrointestinal TractCellular and Molecular NeuroscienceMilkEndocrinologyMineral bioavailabilityMilk productsFruitAnimalsHumansDigestionAmino Acid SequenceFood scienceDigestion
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