Search results for "Cell Membrane"

showing 10 items of 635 documents

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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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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Molecular mechanisms determining the strength of receptor-mediated intermembrane adhesion

1995

The strength of receptor-mediated cell adhesion is directly controlled by the mechanism of cohesive failure between the cell surface and underlying substrate. Unbinding can occur either at the locus of the specific bond or within the bilayer, which results in tearing the hydrophobic anchors from the membrane interior. In this work, the surface force apparatus has been used to investigate the relationship between the receptor-ligand bond affinities and the dominant mechanism of receptor-coupled membrane detachment. The receptors and ligands used in this study were membrane-bound streptavidin and biotin analogs, respectively, with solution affinities ranging over 10 orders of magnitude. With …

StreptavidinStereochemistryLipid BilayersMolecular ConformationBiophysicsReceptors Cell Surface02 engineering and technologyModels BiologicalCell membrane03 medical and health scienceschemistry.chemical_compoundBacterial ProteinsmedicineCell AdhesionAnimalsBond energyLipid bilayer030304 developmental biologyFluorescent Dyes0303 health sciencesThioctic AcidBilayerPhosphatidylethanolaminesCell MembraneSurface forces apparatus021001 nanoscience & nanotechnologyAffinitiesModels StructuralKineticsmedicine.anatomical_structureMembranechemistryBiophysicsStreptavidin0210 nano-technologyAzo CompoundsResearch ArticleBiophysical Journal
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Echovirus 1 Endocytosis into Caveosomes Requires Lipid Rafts, Dynamin II, and Signaling EventsV⃞

2004

Binding of echovirus 1 (EV1, a nonenveloped RNA virus) to the α2β1 integrin on the cell surface is followed by endocytic internalization of the virus together with the receptor. Here, video-enhanced live microscopy revealed the rapid uptake of fluorescently labeled EV1 into mobile, intracellular structures, positive for green fluorescent protein-tagged caveolin-1. Partial colocalization of EV1 with SV40 (SV40) and cholera toxin, known to traffic via caveosomes, demonstrated that the vesicles were caveosomes. The initiation of EV1 infection was dependent on dynamin II, cholesterol, and protein phosphorylation events. Brefeldin A, a drug that prevents SV40 transport, blocked the EV1 infection…

SucroseTime FactorsvirusesEndocytic cycleDynamin IIchemistry.chemical_compoundDynamin IIPhosphorylationInternalizationCytoskeletonIn Situ HybridizationIn Situ Hybridization Fluorescencemedia_commonGenes Dominant0303 health sciencesMicroscopy Videobiology030302 biochemistry & molecular biologyArticlesBrefeldin AEndocytosisCell biologyEnterovirus B HumanCholesterolRNA ViralElectrophoresis Polyacrylamide GelProtein BindingSignal TransductionCholera Toxinmedia_common.quotation_subjectIntegrinGreen Fluorescent ProteinsImmunoblottingEndocytosisTransfectionCell Line03 medical and health sciencesCapsidMembrane MicrodomainsViral entryCentrifugation Density GradientAnimalsMolecular Biology030304 developmental biologyBinding SitesBrefeldin ACell MembraneCell BiologyKineticschemistryViral replicationMicroscopy Fluorescencebiology.protein
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Surface-exposed Amino Acid Residues of HPV16 L1 Protein Mediating Interaction with Cell Surface Heparan Sulfate

2007

Efficient infection of cells by human papillomaviruses (HPVs) and pseudovirions requires primary interaction with cell surface proteoglycans with apparent preference for species carrying heparan sulfate (HS) side chains. To identify residues contributing to virus/cell interaction, we performed point mutational analysis of the HPV16 major capsid protein, L1, targeting surface-exposed amino acid residues. Replacement of lysine residues 278, 356, or 361 for alanine reduced cell binding and infectivity of pseudovirions. Various combinations of these amino acid exchanges further decreased cell attachment and infectivity with residual infectivity of less than 5% for the triple mutant, suggesting …

Surface PropertiesLysinePlasma protein bindingBiochemistryAntibodieschemistry.chemical_compoundCapsidChlorocebus aethiopsAnimalsHumansComputer SimulationMolecular Biologychemistry.chemical_classificationAlanineInfectivityHeparinLysineCell MembraneCapsomereOncogene Proteins ViralCell BiologyHeparan sulfateAmino acidchemistryBiochemistryCapsidMutagenesisCOS CellsCapsid ProteinsHeparitin SulfateProtein BindingJournal of Biological Chemistry
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Protein-lipid interactions at the air-water interface.

2010

International audience; Protein−lipid interactions play an important role in a variety of fields, for example in pharmaceutical research, biosensing, or food science. However, the underlying fundamental processes that govern the interplay of lipids and proteins are often very complex and are therefore studied using model systems. Here, Langmuir monolayers were used to probe the interaction of a model protein with lipid films at the air−water interface. The protein β-lactoglobulin (βlg) is the major component in bovine milk serum, where it coexists with the milk fat globular membrane. During homogenization of milk, βlg adsorbs to the interface of lipid fat globules and stabilizes the oil-in-…

Surface PropertiesPhospholipidLactoglobulinsHomogenization (chemistry)chemistry.chemical_compoundMonolayerElectrochemistryAnimalsGeneral Materials ScienceDenaturation (biochemistry)Globules of fatSpectroscopyChromatographyAirCell MembraneWaterSurfaces and InterfacesHydrogen-Ion ConcentrationCondensed Matter PhysicsLipid Metabolism[SDV.BBM.BP]Life Sciences [q-bio]/Biochemistry Molecular Biology/BiophysicsMembranechemistryIonic strengthEmulsionBiophysicslipids (amino acids peptides and proteins)CattleProtein BindingLangmuir : the ACS journal of surfaces and colloids
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Pump currents generated by the purified Na+K+-ATPase from kidney on black lipid membranes.

1985

The transport activity of purified Na+K+-ATPase was investigated by measuring the electrical pump current induced on black lipid membranes. Discs containing purified Na+K+-ATPase from pig kidney were attached to planar lipid bilayers in a sandwich-like structure. After the addition of only microM concentrations of an inactive photolabile ATP derivative [P3-1-(2-nitro)phenylethyladenosine 5'-triphosphate, caged ATP] ATP was released after illumination with u.v.-light, which led to a transient current in the system. The transient photoresponse indicates that the discs and the underlying membrane are capacitatively coupled. Stationary pump currents were obtained after the addition of the H+, N…

SwineSodium-Potassium-Exchanging ATPaseLipid BilayersDiaphragm pumpBiologyKidneyGeneral Biochemistry Genetics and Molecular BiologyOuabainValinomycinchemistry.chemical_compoundmedicineAnimalsVanadateNa+/K+-ATPaseLipid bilayerMolecular BiologyIon transporterPhotolysisGeneral Immunology and MicrobiologyGeneral NeuroscienceCell MembraneKineticsBiochemistrychemistryBiophysicsThermodynamicsSodium-Potassium-Exchanging ATPasemedicine.drugResearch Article
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Evidence for a multistep mechanism for cell-cell fusion by herpes simplex virus with mutations in the syn 3 locus using heparin derivatives during fu…

1994

Addition of heparin-Na+ as well as related substances of high and intermediate MW (Arteparon and polyanion SP54) 3 h after infection inhibit fusion from within (FFWI) induced by HSV strains with mutations in the syn 3 locus only. The concentration of heparin-Na+ required to inhibit FFWI is 10-fold higher (1 mg/ml) than that needed to inhibit adsorption. Instead of fusion, cell rounding is observed. The effect is readily reversible. A low MW heparin disaccharide is ineffective. Neomycin, at a concentration of 8 mM, inhibits FFWI induced by all HSV-1 but not HSV-2 strains, whereas adsorption is inhibited at 3 mM. We conclude from our observations that cell-cell fusion (FFWI) induced by syn 3 …

SyncytiumCell fusionHeparinCellMutantGeneral MedicineBiologyGiant CellsVirologyCell membranemedicine.anatomical_structureMutagenesisCell cultureCell surface receptorVirologyChlorocebus aethiopsmedicineVero cellAnimalsSimplexvirusVero CellsCells CulturedArchives of Virology
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Mechanical Regulation of the Cytotoxic Activity of Natural Killer Cells

2020

AbstractMechanosensing has been recently explored for T cells and B cells and is believed to be part of their activation mechanism. Here, we explore the mechanosensing of the third type of lymphocytes – Natural Killer (NK) cells, by showing that they modulate their immune activity in response to changes in the stiffness of a stimulating surface. Interestingly, we found that this immune response is bell-shaped, and peaks for a stiffness of a few hundreds of kPa. This bell-shape behavior was observed only for surfaces functionalized with the activating ligand MHC class I polypeptide-related sequence A (MICA), but not for control surfaces lacking immunoactive functionalities. We found that sti…

T-LymphocytesLymphocyte0206 medical engineeringPopulationCellBiomedical Engineering02 engineering and technologyLigandsMajor histocompatibility complexBiomaterialsCell membraneImmune systemMHC class ImedicineCytotoxic T cellReceptors Immunologiceducationeducation.field_of_studyMechanosensationbiologyChemistryHistocompatibility Antigens Class I021001 nanoscience & nanotechnologyNKG2D020601 biomedical engineeringCell biologyKiller Cells Naturalmedicine.anatomical_structurebiology.proteinReceptor clustering0210 nano-technology
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A Transition Zone Complex Regulates Mammalian Ciliogenesis and Ciliary Membrane Composition

2011

Mutations in genes encoding ciliary components cause ciliopathies, but how many of these mutations disrupt ciliary function is unclear. We investigated Tectonic1 (Tctn1), a regulator of mouse Hedgehog signaling, and found that it is essential for ciliogenesis in some, but not all, tissues. Cell types that do not require Tctn1 for ciliogenesis require it to localize select membrane-associated proteins to the cilium, including Arl13b, AC3, Smoothened and Pkd2. Tctn1 forms a complex with multiple ciliopathy proteins associated with Meckel (MKS) and Joubert (JBTS) syndromes, including Mks1, Tmem216, Tmem67, Cep290, B9d1, Tctn2, and Cc2d2a. Components of the Tectonic ciliopathy complex colocaliz…

TMEM67Inbred C57BLCiliopathiesMedical and Health SciencesMice0302 clinical medicineCerebellumMorphogenesisEye AbnormalitiesEncephalocelePediatricMice Knockout0303 health sciencesPolycystic Kidney DiseasesCiliumCiliary transition zoneBiological SciencesKidney Diseases CysticCell biologyOrgan SpecificityCiliary Motility DisordersKidney DiseasesRabbitsAbnormalitiesMultipleRetinitis PigmentosaCiliary Motility DisordersSignal TransductionKnockoutBiologyRetinaArticle03 medical and health sciencesCysticRare DiseasesCerebellar DiseasesCiliogenesisGeneticsMatrix-Assisted Laser Desorption-IonizationAnimalsHumansAbnormalities MultipleCiliaCiliary membrane030304 developmental biologySpectrometryCell MembraneMembrane ProteinsMassPeptide FragmentsMice Inbred C57BLSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationMutationCiliary baseChickens030217 neurology & neurosurgeryDevelopmental BiologyNature genetics
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