Search results for " Library"

showing 10 items of 734 documents

Enhanced baculovirus-mediated transduction of human cancer cells by tumor-homing peptides.

2006

ABSTRACT Tumor cells and vasculature offer specific targets for the selective delivery of therapeutic genes. To achieve tumor-specific gene transfer, baculovirus tropism was manipulated by viral envelope modification using baculovirus display technology. LyP-1, F3, and CGKRK tumor-homing peptides, originally identified by in vivo screening of phage display libraries, were fused to the transmembrane anchor of vesicular stomatitis virus G protein and displayed on the baculoviral surface. The fusion proteins were successfully incorporated into budded virions, which showed two- to fivefold-improved binding to human breast carcinoma (MDA-MB-435) and hepatocarcinoma (HepG2) cells. The LyP-1 pepti…

Phage displayCarcinoma HepatocellularTransgenevirusesImmunologyBreast NeoplasmsGene deliveryMicrobiologyVesicular stomatitis Indiana virusTransduction (genetics)Gene DeliveryViral envelopePeptide LibraryTransduction GeneticVirologyCell Line TumorHumansGlycoproteinsbiologyGenetic Therapybiology.organism_classificationMolecular biologyFusion proteinNeoplasm ProteinsVesicular stomatitis virusCell cultureInsect ScienceCapsid ProteinsPeptidesBaculoviridaeProtein BindingJournal of virology
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Baculovirus Display: A Multifunctional Technology for Gene Delivery and Eukaryotic Library Development

2006

For over a decade, phage display has proven to be of immense value, allowing selection of a large variety of genes with novel functions from diverse libraries. However, the folding and modification requirements of complex proteins place a severe constraint on the type of protein that can be successfully displayed using this strategy, a restriction that could be resolved by similarly engineering a eukaryotic virus for display purposes. The quite recently established eukaryotic molecular biology tool, the baculovirus display vector system (BDVS), allows combination of genotype with phenotype and thereby enables presentation of eukaryotic proteins on the viral envelope or capsid. Data have sho…

Phage displayExpression vectorViral envelopeCapsidvirusesAntigen presentationComputational biologyGene deliveryBiologyPeptide libraryGeneVirology
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Identification of binding peptides on calcium silicate hydrate: a novel view on cement additives.

2014

Cement is the most used industrial product in the world. Although the chemical composition of the material has stayed more or less the same since its discovery by the Romans around 2000 years ago, [ 1 ] the performance has been increased by chemical additives. Spectacular buildings like the Willis Tower in Chicago, Taipei 101 or lately the over 800 m high Burj Khalifa in Dubai were realizable thanks to the development of high performance building materials. [ 2 ] Not only for such prestige objects but also in daily building processes, the trend goes towards always higher buildings because of the continued urbanization which was identifi ed already in 1982 as one of the so-called “megatrends…

Phage displayMaterials scienceSurface PropertiesSilicic AcidMineralogy02 engineering and technology010402 general chemistry01 natural scienceslaw.inventionchemistry.chemical_compoundlawPeptide LibraryAmideNegative chargeGeneral Materials ScienceAmino Acid SequenceCalcium silicate hydrateComputingMilieux_MISCELLANEOUSCementMechanical EngineeringHydrogen BondingHydrogen-Ion Concentration021001 nanoscience & nanotechnology0104 chemical sciencesPortland cementchemistryChemical engineeringMechanics of MaterialsCalcium silicateddc:540Calcium[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]0210 nano-technologyPeptidesHydrophobic and Hydrophilic InteractionsSilicate CementAdvanced materials (Deerfield Beach, Fla.)
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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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Peptide microarrays enable rapid mimotope optimization for pharmacokinetic analysis of the novel therapeutic antibody IMAB362.

2014

As membrane proteins play an important role in a variety of life-threatening diseases, the development of therapeutic monoclonal antibodies against membrane proteins is of significant interest. Among many other requirements, the process of antibody drug development requires a set of tailor-made assays for the characterization of the antibodies and for monitoring their activity. Designing assays to characterize antibodies directed to membrane proteins is challenging, because the natural targets are often not available in a format that is compatible with a biochemical assay setup. Thus, alternatives that mimic the targeted membrane proteins are needed. In this study, we developed optimal pept…

Phage displaymedicine.drug_classProtein Array AnalysisEnzyme-Linked Immunosorbent AssayComputational biologyBiologyMonoclonal antibodyApplied Microbiology and BiotechnologyStructure-Activity RelationshipPeptide LibrarymedicineAnimalsIMAB362Mice Inbred BALB CMimotopeAssayAntibodies MonoclonalGeneral MedicineMolecular biologyMembrane proteinDrug developmentMolecular MedicineFemaleDNA microarrayPeptidesProtein BindingBiotechnology journal
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Structure of the phenylalanine hydroxylase gene in Drosophila melanogaster and evidence of alternative promoter usage.

1996

The complete Drosophila melanogaster phenylalanine hydroxylase gene isolated from a genomic library was sequenced. Gene structure consisted of five exons covering a region of around 3 kb. Position of introns in the C-terminal domain was conserved with mammalian aromatic amino acid hydroxylase genes. Putative promoter sequences in the 5'UTR and intron 1 were identified. A novel transcript was detected differing from that previously reported by the inclusion of a part of the intron 1 sequence. It could be produced using an alternative promoter. The deduced open reading frame would code a protein with a small difference at the N-terminus. Expression of the alternative transcripts was examined …

Phenylalanine hydroxylaseTranscription GeneticMolecular Sequence DataBiophysicsGenes InsectBiochemistryPolymerase Chain ReactionExonchemistry.chemical_compoundAromatic amino acidsAnimalsGenomic libraryAmino Acid SequenceRNA MessengerPromoter Regions GeneticMolecular BiologyGeneDNA PrimersGeneticsGenomic LibrarybiologyBase SequenceIntronPhenylalanine HydroxylaseCell BiologyExonsbiology.organism_classificationMolecular biologyIntronsOpen reading frameDrosophila melanogasterchemistrybiology.proteinDrosophila melanogasterBiochemical and biophysical research communications
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La aporofobia como desafío antropológico. De la lógica de la cooperación a la lógica del reconocimiento

2019

el objetivo de este trabajo es poner en relación el núcleo crítico de la última obra de Adela Cortina, Aporofobia, que puede ser resu- mido como una protesta contra los límites del paradigma de la cooperación y la reciprocidad, con algunos elementos aparecidos en obras ante- riores de la autora 1 . Para ello expondré primero algunos límites y virtualidades del paradigma de la reciprocidad. Tras bosquejar el núcleo de la obra Aporofobia, deteniéndome en los lugares en que este problema se hace más patente, terminaré rastreando algunos lugares anteriores en los que la autora anticipaba ya, desde una óptica diferente, esta misma crítica. he aim of this paper is to connect the critical core of …

Philosophy0508 media and communicationsPhilosophy05 social sciencesreconocimiento1(05)Aporofobia050801 communication & media studies0509 other social sciences050904 information & library sciencescooperaciónHumanitiesreciprocidadDaímon
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Solid-Phase Synthesis of Peptide Libraries Combining α-Amino Acids with Inorganic and Organic Chromophores

2009

The synthesis of two series of peptidic chains composed of bis(terpyridine)ruthenium(II) acceptor units and organic chromophores (coumarin, naphthalene, anthracene, fluorene) by stepwise solid-phase peptide synthesis (SPPS) techniques is described. The first series of dyads comprises directly amide linked chromophores, while the second one possesses a glycine spacer between the two chromophores. All dyads were studied by UV/Vis and NMR spectroscopy, steady-state luminescence, luminescence decay and electrochemistry, as well as by DFT calculations. The results of these studies indicate weak electronic coupling of the chromophores in the ground state. Absorption spectra of all dyads are domin…

Photochemistrychemistry.chemical_elementNaphthalenesFluorenePhotochemistryRutheniumCatalysischemistry.chemical_compoundCoumarinsPeptide LibraryElectrochemistryAmino AcidsColoring AgentsAnthracenesFluorenesAnthraceneQuenching (fluorescence)Spectrum AnalysisOrganic ChemistryGeneral ChemistryNuclear magnetic resonance spectroscopyChromophoreRutheniumchemistryTerpyridinePeptidesLuminescenceChemistry - A European Journal
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Identification of Novel Molecular Components of the Photoreceptor Connecting Cilium by Immunoscreens

2002

Abstract The connecting cilium of photoreceptor cells is the only intracellular link between the morphologically, functionally and biochemically different compartments of the inner and outer segments. The non-motile modified cilium plays an important role in the organization and the function of photoreceptor cells, namely in delivery and turnover of enzymes and substrates of the visual transduction cascade, and the photosensitive membranes of the outer segment. The protein components of the cilium participate in the intracellular transport through the cilium, in the outer segment disk morphogenesis and in the maintenance of discrete membrane domains. In order to identify yet unknown cytoske…

Photoreceptor Connecting CiliumAdenomatous Polyposis Coli ProteinXenopus ProteinsBiologyPhotoreceptor cellRats Sprague-DawleyMiceCellular and Molecular NeurosciencemedicineAnimalsDrosophila ProteinsCiliaCloning MolecularCytoskeletonMicrotubule-Associated Protein 4CytoskeletonGene LibraryRetinaCiliumCalcium-Binding ProteinsDynactin ComplexSensory SystemsRatsCell biologyMice Inbred C57BLOphthalmologymedicine.anatomical_structureCentrinsense organsMicrotubule-Associated ProteinsPhotoreceptor Cells VertebrateVisual phototransductionExperimental Eye Research
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Single amino acids in the lumenal loop domain influence the stability of the major light-harvesting chlorophyll a/b complex.

2004

The major light-harvesting complex of photosystem II (LHCIIb) is one of the most abundant integral membrane proteins. It greatly enhances the efficiency of photosynthesis in green plants by binding a large number of accessory pigments that absorb light energy and conduct it toward the photosynthetic reaction centers. Most of these pigments are associated with the three transmembrane and one amphiphilic alpha helices of the protein. Less is known about the significance of the loop domains connecting the alpha helices for pigment binding. Therefore, we randomly exchanged single amino acids in the lumenal loop domain of the bacterially expressed apoprotein Lhcb1 and then reconstituted the muta…

Photosynthetic reaction centreProtein FoldingPhotosystem IIPigment bindingDNA Mutational AnalysisLight-Harvesting Protein ComplexesPeasPhotosystem II Protein ComplexBiologyBiochemistryTransmembrane proteinProtein Structure SecondaryProtein Structure TertiaryB vitaminsBiochemistryAmino Acid SubstitutionMutant proteinMutagenesis Site-DirectedPoint MutationAmino AcidsIntegral membrane proteinAccessory pigmentGene LibraryPlant ProteinsBiochemistry
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