Search results for "Biotinylation"

showing 10 items of 76 documents

Adsorption and Conformation Behavior of Biotinylated Fibronectin on Streptavidin-Modified TiOX Surfaces Studied by SPR and AFM

2011

It is well-known that protein-modified implant surfaces such as TiO(2) show a higher bioconductivity. Fibronectin is a glycoprotein from the extracellular matrix (ECM) with a major role in cell adhesion. It can be applied on titanium oxide surfaces to accelerate implant integration. Not only the surface concentration but also the presentation of the protein plays an important role for the cellular response. We were able to show that TiO(X) surfaces modified with biotinylated fibronectin adsorbed on a streptavidin-silane self-assembly multilayer system are more effective regarding osteoblast adhesion than surfaces modified with nonspecifically bound fibronectin. The adsorption and conformati…

StreptavidinConformational changeProtein ConformationSurface PropertiesBiotinNanotechnologyMicroscopy Atomic Forcechemistry.chemical_compoundAdsorptionMonolayerElectrochemistryGeneral Materials ScienceSurface plasmon resonanceSpectroscopyTitaniumbiologyChemistrytechnology industry and agricultureSurfaces and InterfacesAdhesionSurface Plasmon ResonanceCondensed Matter PhysicsFibronectinsFibronectinBiotinylationbiology.proteinBiophysicsAdsorptionStreptavidinLangmuir
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Engineering of chicken avidin: a progressive series of reduced charge mutants.

1998

Avidin, a positively charged egg-white glycoprotein, is a widely used tool in biotechnological applications because of its ability to bind biotin strongly. The high pI of avidin (approximately 10.5), however, is a hindrance in certain applications due to non-specific (charge-related) binding. Here we report a construction of a series of avidin charge mutants with pIs ranging from 9.4 to 4.7. Rational design of the avidin mutants was based on known crystallographic data together with comparative sequence alignment of avidin, streptavidin and a set of avidin-related genes which occur in the chicken genome. All charge mutants retained the ability to bind biotin tightly according to optical bio…

StreptavidinDNA ComplementaryHot TemperatureMutantBiophysicsBiotinSequence alignmentBiologySpodopteraProtein EngineeringBiochemistrychemistry.chemical_compoundstomatognathic systemBiotinStructural BiologyGeneticsAnimalsMolecular BiologyCharge mutantAvidin-biotin technologyRational designCell BiologyProtein engineeringrespiratory systemAvidinDNA-Binding ProteinschemistryBiochemistryBiotinylationbiology.proteinMutagenesis Site-DirectedChickensAvidinFEBS letters
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Recombinant NeutraLite Avidin: a non-glycosylated, acidic mutant of chicken avidin that exhibits high affinity for biotin and low non-specific bindin…

2000

AbstractA recombinant non-glycosylated and acidic form of avidin was designed and expressed in soluble form in baculovirus-infected insect cells. The mutations were based on the same principles that guided the design of the chemically and enzymatically modified avidin derivative, known as NeutraLite Avidin. In this novel recombinant avidin derivative, five out of the eight arginine residues were replaced with neutral amino acids, and two of the lysine residues were replaced by glutamic acid. In addition, the carbohydrate-bearing asparagine-17 residue was altered to an isoleucine, according to the known sequences of avidin-related genes. The resultant mutant protein, termed recombinant Neutr…

StreptavidinGlycosylationMolecular Sequence DataBiophysicsBiotinChick EmbryoNon-specific bindingBiochemistrylaw.inventionchemistry.chemical_compoundBiotinstomatognathic systemStructural BiologylawMutant proteinNon-glycosylated mutantGeneticsAnimalsHumansAmino Acid SequenceIsoelectric PointProtein Structure QuaternaryMolecular BiologyCells CulturedbiologyAvidin-biotin technologyDNACell BiologyProtein engineeringrespiratory systemAvidinRecombinant ProteinsKineticsAmino Acid SubstitutionchemistryBiochemistryBiotinylationMutationbiology.proteinRecombinant DNAThermodynamicsProtein engineeringEndopeptidase KIsoleucineBaculoviridaeProtein BindingAvidinFEBS Letters
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Recombinant avidin and avidin-fusion proteins.

2000

Both chicken egg-white avidin and its bacterial relative streptavidin are well known for their extraordinary high affinity with biotin (Kd approximately 10(-15) M). They are widely used as tools in a number of affinity-based separations, in diagnostic assays and in a variety of other applications. These methods have collectively become known as (strept)avidin-biotin technology. Biotin can easily and effectively be attached to different molecules, termed binders and probes, without destroying their biological activity. The exceptional stability of the avidin-biotin complex and the wide range of commercially available reagents explain the popularity of this system. In order by genetic enginee…

StreptavidinInsectaAffinity labelRecombinant Fusion ProteinsBiotinBioengineeringProtein Engineeringlaw.inventionchemistry.chemical_compoundstomatognathic systemBiotinlawEscherichia coliAnimalsMolecular BiologybiologyCell MembraneAffinity LabelsProtein engineeringrespiratory systemAvidinFusion proteinRecombinant ProteinschemistryBiochemistryBiotinylationRecombinant DNAbiology.proteinBaculoviridaeChickensBiotechnologyAvidinBiomolecular engineering
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Formation of protein multilayers and their competitive replacement based on self-assembled biotinylated phospholipids.

1994

Based on specific recognition processes the build-up of protein multilayers was achieved using streptavidin layers as a docking matrix. For this purpose, streptavidin was organized at biotin-containing monolayers, liposomes, and self-assembled layers on gold. Thus, mixed double and triple layers of streptavidin, Con A, Fab fragments, and hormones were prepared and characterized by fluorescence microscopy and plasmon spectroscopy. Using biotin analogues with lower binding constants several cycles of multilayer formation followed by competitive replacement could be achieved.

StreptavidinLiposomeSurface Propertiestechnology industry and agricultureBiomedical EngineeringBiophysicsBiotinProteinsBioengineeringBinding CompetitiveBiomaterialsCrystallographychemistry.chemical_compoundMolecular recognitionBiotinchemistryBacterial ProteinsDocking (molecular)BiotinylationMonolayerFluorescence microscopeStreptavidinPhospholipidsJournal of biomaterials science. Polymer edition
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Protein-membrane interaction probed by single plasmonic nanoparticles.

2008

We present a nanosized and addressable sensor platform based on membrane coated plasmonic particles and show unequivocally the covering with lipid bilayers as well as the subsequent detection of streptavidin binding to biotinylated lipids. The binding is detected on membrane covered gold nanorods by monitoring the spectral shift by fast single particle spectroscopy (fastSPS) on many particles in parallel. Our approach allows for local analysis of protein interaction with biological membranes as a function of the lateral composition of phase separated membranes.

StreptavidinMaterials scienceNanoparticleMolecular Probe TechniquesBioengineeringNanotechnologyResonance (particle physics)Spectral lineQuantitative Biology::Subcellular Processeschemistry.chemical_compoundProtein Interaction MappingGeneral Materials ScienceSurface plasmon resonanceSpectroscopyLipid bilayerPlasmonPlasmonic nanoparticlesbusiness.industryChemistryMechanical EngineeringCell MembraneMembrane ProteinsBiological membraneGeneral ChemistrySurface Plasmon ResonanceCondensed Matter PhysicsDark field microscopyMembraneTransmission electron microscopyBiotinylationParticleOptoelectronicsNanoparticlesbusinessNano letters
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Reactive Surface Coatings Based on Polysilsesquioxanes: Controlled Functionalization for Specific Protein Immobilization

2009

The key designing in reliable biosensors is the preparation of thin films in which biomolecular functions may be immobilized and addressed in a controlled and reproducible manner. This requires the controlled preparation of specific binding sites on planar surfaces. Poly(methylsilsesquioxane)-poly(pentafluorophenyl acrylates) (PMSSQ-PFPA) are promising materials to produce stable and adherent thin reactive coatings on various substrates. Those reactive surface coatings could be applied onto various materials, for example, gold, polycarbonate (PC), poly(tetrafluoroethylene) (PTFE), and glass. By dipping those substrates in a solution of a desired amine, specific binding sites for protein ads…

StreptavidinMaterials sciencePolymersSurface PropertiesBiotinInfrared spectroscopyMicroscopy Atomic Forcechemistry.chemical_compoundAdsorptionSpectroscopy Fourier Transform InfraredElectrochemistryOrganic chemistryBiotinylationOrganosilicon CompoundsGeneral Materials ScienceFourier transform infrared spectroscopySurface plasmon resonanceFuransPolytetrafluoroethyleneSpectroscopyPolycarboxylate CementTemperaturetechnology industry and agricultureProteinsSurfaces and InterfacesCondensed Matter PhysicsAmidesQuaternary Ammonium CompoundsModels ChemicalchemistryChemical engineeringSurface modificationGlassBiosensorProtein adsorptionLangmuir
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Streptavidin-coated TiO2 surfaces are biologically inert: Protein adsorption and osteoblast adhesion studies

2011

Non-fouling TiO2 surfaces are attractive for a wide range of applications such as biosensors and medical devices, where biologically inert surfaces are needed. Typically, this is achieved by controlled surface modifications which prevent protein adsorption. For example, polyethylene glycol (PEG) or PEG-derived polymers have been widely applied to render TiO2 surfaces biologically inert. These surfaces have been further modified in order to achieve specific bio-activation. Therefore, there have been efforts to specifically functionalize TiO2 surfaces with polymers with embedded biotin motives, which can be used to couple streptavidin for further functionalization. As an alternative, here a s…

StreptavidinMaterials scienceSurface PropertiesBiomedical EngineeringNanotechnologyMicroscopy Atomic ForceCell LineBiomaterialschemistry.chemical_compoundCell AdhesionHumansBiotinylationTitaniumchemistry.chemical_classificationOsteoblaststechnology industry and agricultureMetals and AlloysPolymerSilanesFibronectinsKineticsSurface coatingchemistryBiotinylationCeramics and CompositesSurface modificationMuramidaseAdsorptionStreptavidinBiosensorLayer (electronics)Protein adsorptionJournal of Biomedical Materials Research Part A
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Layer-by-Layer Assembly of a Streptavidin–Fibronectin Multilayer on Biotinylated TiOX

2013

The biomodification of surfaces, especially titanium, is an important issue in current biomedical research. Regarding titanium, it is also important to ensure a specific protein modification of its surface because here protein binding that is too random can be observed. Specific nanoscale architectures can be applied to overcome this problem. As recently shown, streptavidin can be used as a coupling agent to immobilize biotinylated fibronectin (bFn) on a TiO(X) surface. Because of the conformation of adsorbed biotinylated fibronectin on a streptavidin monolayer, it is possible to adsorb more streptavidin and biotinylated fibronectin layers. On this basis, an alternating protein multilayer c…

StreptavidinMaterials sciencechemistry.chemical_compoundAdsorptionBiotinMonolayerElectrochemistryBiotinylationGeneral Materials ScienceSpectroscopyFluorescent DyesTitaniumbiologyLayer by layertechnology industry and agriculturefood and beveragesSurfaces and InterfacesCondensed Matter PhysicsFibronectinsFibronectinSpectrometry FluorescencechemistryBiotinylationbiology.proteinBiophysicsAdsorptionStreptavidinLayer (electronics)Langmuir
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Dimer-tetramer transition between solution and crystalline states of streptavidin and avidin mutants.

2003

ABSTRACT The biotin-binding tetrameric proteins, streptavidin from Streptomyces avidinii and chicken egg white avidin, are excellent models for the study of subunit-subunit interactions of a multimeric protein. Efforts are thus being made to prepare mutated forms of streptavidin and avidin, which would form monomers or dimers, in order to examine their effect on quaternary structure and assembly. In the present communication, we compared the crystal structures of binding site W→K mutations in streptavidin and avidin. In solution, both mutant proteins are known to form dimers, but upon crystallization, both formed tetramers with the same parameters as the native proteins. All of the intersub…

StreptavidinModels MolecularStereochemistryProtein ConformationDimerBiotinCrystallography X-RayMicrobiologychemistry.chemical_compoundProtein structureBiotinTetramerEgg WhiteStructural BiologyAnimalsProtein Structure QuaternaryMolecular BiologyBinding SitesbiologyAvidinStreptomycesSolutionschemistryBiochemistryBiotinylationMutationbiology.proteinProtein quaternary structureStreptavidinCarrier ProteinsCrystallizationChickensDimerizationAvidinJournal of bacteriology
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