Search results for "Viral protein"

showing 10 items of 182 documents

Proliferation and MHC-unrestricted bystander lysis by virus-specific cytotoxic T cells following antigen self-presentation.

1998

Cytotoxic T cells (CTL) not only act as effector cells, but can also serve as antigen-presenting cells (APC) for other CTL due to their expression of major histocompatibility complex (MHC) class I molecules. In the present study we show that independently derived CTL lines (CTLL) with specificity for an L(d)-presented nonapeptide corresponding to amino acids 168-176 of the immediate-early 1 (IE1) protein of murine cytomegalovirus not only lyse syngeneic but also allogeneic target cells, if the peptide is present during the cytolytic assay. Whereas a short peptide pulse is sufficient to render syngeneic cells susceptible to lysis, continued presence of soluble peptide is mandatory for the ly…

Microbiology (medical)ImmunologyAntigen presentationMajor histocompatibility complexLymphocyte ActivationImmediate early proteinImmediate-Early ProteinsMajor Histocompatibility ComplexMiceViral ProteinsAntigenmedicineTumor Cells CulturedImmunology and AllergyCytotoxic T cellAnimalsAntigens ViralB cellCells CulturedAntigen PresentationMice Inbred BALB CbiologyHistocompatibility Antigens Class IGeneral MedicineVirologyMolecular biologyCytolysisCTL*medicine.anatomical_structurebiology.proteinT-Lymphocytes CytotoxicMedical microbiology and immunology
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Molecular characterization of genotype G6 human rotavirus strains detected in Italy from 1986 to 2009.

2011

Group A human rotavirus (HRV) strains with a bovine-like (G6) major outer capsid protein VP7 were first detected in Palermo, Italy, in the late 1980s, and subsequently worldwide. During a 25-year rotavirus surveillance period, additional HRV G6 strains, associated with either a P[9] or P[14] VP4 genotype, have been detected sporadically, but repeatedly, in Palermo. Whether these G6 HRVs were transmitted to humans directly from an animal reservoir or could have circulated at low prevalence in susceptible individuals is uncertain. Upon sequence analyses of the VP7, VP4, VP6, NSP4 and NSP5 gene segments, all the Italian HRV strains displayed a conserved genotype constellation, G6-P[9]/[14]-I2-…

Microbiology (medical)RotavirusGenotypingSettore MED/07 - Microbiologia E Microbiologia ClinicaLineage (genetic)GenotypevirusesPeriod (gene)Biologymedicine.disease_causeMicrobiologyGroup ARotavirus InfectionsViral ProteinsRotavirusGenotypeGeneticsmedicineAnimalsHumansMolecular BiologyGenotypingGeneG6Ecology Evolution Behavior and SystematicsPhylogenyGeneticsTransmission (medicine)Sequence Analysis RNAvirus diseasesRotaviruVirologyP[9]Infectious DiseasesItalyP[14]Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases
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Free Chlorine and Peroxynitrite Alter the Capsid Structure of Human Norovirus GII.4 and Its Capacity to Bind Histo-Blood Group Antigens

2021

Human noroviruses (HuNoVs) are one of the leading causes of acute gastroenteritis worldwide. HuNoVs are frequently detected in water and foodstuffs. Free chlorine and peroxynitrite (ONOO−) are two oxidants commonly encountered by HuNoVs in humans or in the environment during their natural life cycle. In this study, we defined the effects of these two oxidants on GII.4 HuNoVs and GII.4 virus-like particles (VLPs). The impact on the capsid structure, the major capsid protein VP1 and the ability of the viral capsid to bind to histo-blood group antigens (HBGAs) following oxidative treatments were analyzed. HBGAs are attachment factors that promote HuNoV infection in human hosts. Overall, our re…

Microbiology (medical)viral proteinViral protein[SDV]Life Sciences [q-bio]viruseslcsh:QR1-502noroviruschemistry.chemical_elementvirus-like particlesmedicine.disease_causeMicrobiologylcsh:MicrobiologyperoxynitriteMicrobiologyBlood group antigens03 medical and health scienceschemistry.chemical_compoundAntigenmedicineChlorineOriginal Research030304 developmental biologyNorovirus GII0303 health sciences030306 microbiologyChemistryvirus diseasesfree chlorinebiochemical phenomena metabolism and nutrition3. Good healthCapsid[SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/VirologyNorovirushisto-blood group antigensPeroxynitriteFrontiers in Microbiology
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Social evolution of innate immunity evasion in a virus

2019

Antiviral immunity has been studied extensively from the perspective of virus−cell interactions, yet the role of virus−virus interactions remains poorly addressed. Here, we demonstrate that viral escape from interferon (IFN)-based innate immunity is a social process in which IFN-stimulating viruses determine the fitness of neighbouring viruses. We propose a general and simple social evolution framework to analyse how natural selection acts on IFN shutdown and validate it in cell cultures and mice infected with vesicular stomatitis virus. Furthermore, we find that IFN shutdown is costly because it reduces short-term viral progeny production, thus fulfilling the definition of an altruistic tr…

Microbiology (medical)virusesImmunologyBiologyApplied Microbiology and BiotechnologyMicrobiologyAntiviral AgentsModels BiologicalArticleVirusVesicular stomatitis Indiana virus03 medical and health sciencesMiceViral ProteinsInterferonImmunityGeneticsmedicineAnimals030304 developmental biologyImmune Evasion0303 health sciencesMice Inbred BALB CInnate immune systemNatural selection030306 microbiologyBrainCell BiologyDNA-Directed RNA Polymerasesbiology.organism_classificationAltruismVirologyBiological EvolutionImmunity Innate3. Good healthDisease Models AnimalVesicular stomatitis virusViral evolutionHost-Pathogen InteractionsFemaleInterferonsSocial evolutionmedicine.drugNature Microbiology
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Tetraspanins in infections by human cytomegalo- and papillomaviruses

2017

Members of the tetraspanin family have been identified as essential cellular membrane proteins in infectious diseases by nearly all types of pathogens. The present review highlights recently published data on the role of tetraspanin CD151, CD81, and CD63 and their interaction partners in host cell entry by human cytomegalo- and human papillomaviruses. Moreover, we discuss a model for tetraspanin assembly into trafficking platforms at the plasma membrane. These platforms might persist during intracellular viral trafficking.

Models Molecular0301 basic medicineCellular membraneTetraspaninsCytomegalovirusTetraspanin 24BiologyEndocytosismedicine.disease_causeBiochemistryTetraspanin 28Viral Proteins03 medical and health sciencesTetraspaninmedicineHumansPapillomaviridaeCD151Tetraspanin 30Cell MembranePapillomavirus InfectionsCytomegalovirusVirus InternalizationVirologyCell biology030104 developmental biologyCytomegalovirus Infectionsembryonic structuresIntracellularCD81Biochemical Society Transactions
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Isolation and Characterization of Two Klebsiella pneumoniae Phages Encoding Divergent Depolymerases

2020

The emergence of multidrug-resistant bacteria is a major global health concern. The search for new therapies has brought bacteriophages into the spotlight, and new phages are being described as possible therapeutic agents. Among the bacteria that are most extensively resistant to current antibiotics is Klebsiella pneumoniae, whose hypervariable extracellular capsule makes treatment particularly difficult. Here, we describe two new K. pneumoniae phages, &pi

Models Molecular0301 basic medicineKlebsiellaPhage therapyKlebsiella pneumoniae<i>Klebsiella pneumoniae</i>virusesmedicine.medical_treatmentAntibioticsMolecular Conformationlcsh:ChemistryBacteriophagebacteriophagewide infection rangeBacteriophagesAntigens Virallcsh:QH301-705.5PhylogenySpectroscopybiologyGeneral Medicine3. Good healthComputer Science ApplicationsKlebsiella pneumoniaePhenotypephage therapyPhage therapymedicine.drug_class030106 microbiologyGenome ViralArticleHost SpecificityCatalysisMicrobiologyInorganic ChemistryViral Proteins03 medical and health sciencesPodoviridaeBacteriolysismedicineAmino Acid SequencePhysical and Theoretical ChemistryBacteriophageMolecular BiologyTropismWhole Genome SequencingOrganic ChemistryComputational BiologyGenetic VariationMolecular Sequence Annotationbiology.organism_classificationKlebsiella Infections030104 developmental biologylcsh:Biology (General)lcsh:QD1-999Wide infection rangeBacteriaInternational Journal of Molecular Sciences
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Determination of enrichment factors for modified RNA in MeRIP experiments

2019

In the growing field of RNA modification, precipitation techniques using antibodies play an important role. However, little is known about their specificities and protocols are missing to assess their effectiveness. Here we present a method to assess enrichment factors after MeRIP-type pulldown experiments, here exemplified with a commercial antibody against N6-methyladenosine (m6A). Testing different pulldown and elution conditions, we measure enrichment factors of 4-5 using m6A-containing mRNAs against an unmodified control of identical sequence. Both types of mRNA carry 32P labels at different nucleotides, allowing their relative quantification in a mixture after digestion to nucleotides…

Models MolecularAdenosineAbsolute quantificationMethylationProtein Structure SecondaryGeneral Biochemistry Genetics and Molecular BiologyViral Proteins03 medical and health sciencesAdenosine TriphosphateRNA modificationEscherichia coliHumansImmunoprecipitationProtein Interaction Domains and MotifsNucleotideRNA MessengerMolecular Biology030304 developmental biologychemistry.chemical_classification0303 health sciencesMessenger RNACell-Free SystemChemistryElution030302 biochemistry & molecular biologyRNADNA-Directed RNA PolymerasesBiochemistryImmunoglobulin GIsotope LabelingChromatography Thin LayerPhosphorus RadioisotopesProtein BindingMethods
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Charge Pair Interactions in Transmembrane Helices and Turn Propensity of the Connecting Sequence Promote Helical Hairpin Insertion

2013

alpha-Helical hairpins, consisting of a pair of closely spaced transmembrane (TM) helices that are connected by a short interfacial turn, are the simplest structural motifs found in multi-spanning membrane proteins. In naturally occurring hairpins, the presence of polar residues is common and predicted to complicate membrane insertion. We postulate that the pre-packing process offsets any energetic cost of allocating polar and charged residues within the hydrophobic environment of biological membranes. Consistent with this idea, we provide here experimental evidence demonstrating that helical hairpin insertion into biological membranes can be driven by electrostatic interactions between clo…

Models MolecularBioquímicaProtein FoldingGlycosylationMolecular Sequence Datamembrane integrationEndoplasmic Reticulumsalt bridgeProtein Structure SecondaryTurn (biochemistry)Viral Proteins03 medical and health sciencesProtein structureStructural BiologyComputer SimulationAmino Acid SequenceAmino AcidsStructural motifMolecular Biologytranslocon030304 developmental biology0303 health sciencesBinding SitesChemistry030302 biochemistry & molecular biologyProteïnes de membranaBiochemistry and Molecular BiologyMembrane ProteinsBiological membraneTransloconelectrostatic interactionsTransmembrane proteinProtein Structure TertiaryPoliovirusProtein TransportCrystallographyTransmembrane domainhelical hairpinMembrane proteinMutationBiophysicsElectrophoresis Polyacrylamide GelHydrophobic and Hydrophilic InteractionsBiokemi och molekylärbiologi
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Structure and Dynamics of RNA Guanine Quadruplexes in SARS-CoV-2 Genome. Original Strategies against Emerging Viruses

2021

Guanine quadruplex (G4) structures in the viral genome have a key role in modulating viruses' biological activity. While several DNA G4 structures have been experimentally resolved, RNA G4s are definitely less explored. We report the first calculated G4 structure of the RG-1 RNA sequence of SARS-CoV-2 genome, obtained by using a multiscale approach combining quantum and classical molecular modeling and corroborated by the excellent agreement between the corresponding calculated and experimental circular dichroism spectra. We prove the stability of the RG-1 G4 arrangement as well as its interaction with G4 ligands potentially inhibiting viral protein translation.

Models MolecularLetterMolecular modelSARS-CoV-2ChemistryViral proteinGuanineCOVID-19RNATranslation (biology)Genome ViralComputational biologymedicine.disease_causeG-quadruplexGenomeG-Quadruplexeschemistry.chemical_compoundSettore CHIM/03 - Chimica Generale E InorganicamedicineHumansNucleic Acid ConformationRNA ViralGeneral Materials SciencePhysical and Theoretical ChemistryDNAThe Journal of Physical Chemistry Letters
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Evidence for substrate binding-induced zwitterion formation in the catalytic Cys-His dyad of the SARS-CoV main protease.

2014

The coronavirus main protease (M(pro)) represents an attractive drug target for antiviral therapy of coronavirus (CoV) infections, including severe acute respiratory syndrome (SARS). The SARS-CoV M(pro) and related CoV proteases have several distinct features, such as an uncharged Cys-His catalytic dyad embedded in a chymotrypsin-like protease fold, that clearly separate these enzymes from archetypical cysteine proteases. To further characterize the catalytic system of CoV main proteases and to obtain information about improved inhibitors, we performed comprehensive simulations of the proton-transfer reactions in the SARS-CoV M(pro) active site that lead to the Cys(-)/His(+) zwitterionic st…

Models MolecularProteasesStereochemistryvirusesmedicine.medical_treatmentEntropyStatic ElectricityMolecular Dynamics Simulationmedicine.disease_causeBiochemistrySubstrate Specificitychemistry.chemical_compoundViral ProteinsCatalytic DomainmedicineHistidineCysteineHistidineCoronavirus 3C ProteasesCoronaviruschemistry.chemical_classificationProteasebiologyChemistryvirus diseasesActive siteCysteine EndopeptidasesEnzymeBiochemistryZwitterionbiology.proteinCysteineBiochemistry
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