Search results for "affinity"

showing 10 items of 313 documents

Sugar specific cellular lectins of Phallusia mamillata hemocytes: Purification, characterization and evidence for cell surface localization

1989

Cellular lectins (CLs) of Phallusia mamillata were demonstrated in protein preparations obtained by salt fractionation from hemocytes sonicated in a suitable medium. Since the lectins from the precipitated fraction bind sugars containing D-galactosyl groups, they were purified by affinity chromatography on Sepharose. SDS-PAGE under reducing conditions showed that CLs are formed of two components of apparent MWs approximately 36,900 and 35,090 and thus differ from serum lectins (SLs) (MW about 62,200). The "shrinkage" observed when SLs were examined under nonreducing conditions suggest the presence of intrachain disulphide bonds which can affect the molecular structure of the SLs. CL-SL diff…

PhallusiaHemocytesImmunologyLactoseHemocyteImmunoelectrophoresisTunicateChromatography AffinitySepharoseAffinity chromatographyLectinsmedicineAnimalsUrochordatachemistry.chemical_classificationGel electrophoresisBlood Cellsbiologymedicine.diagnostic_testCell MembraneLectinHemagglutination Inhibition Testsbiology.organism_classificationImmunodiffusionMolecular WeightchemistryBiochemistrybiology.proteinGlycoproteinLectinDevelopmental Biology
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Isolation of endothelin A receptor from bovine lungs.

1995

We isolated endothelin receptor A (ET A ) from bovine lungs in a single-step purification procedure using antibodies raised against synthetic peptides that correspond to extra- and intracellular domains of the rat bradykinin receptor. Two receptor species of 55 and 35 kDa were isolated and subjected to N-terminal microsequencing. The difference between the observed and expected molecular weight species suggests that bovine ET A receptor is glycosylated.

PharmacologyGlycosylationReceptors EndothelinBiologyIn vitroRatsMolecular Weightchemistry.chemical_compoundBiochemistryAffinity chromatographychemistrybiology.proteinAnimalsCattleRabbitsAntibodyBradykinin receptorCardiology and Cardiovascular MedicineEndothelin receptorReceptorLungIntracellularJournal of cardiovascular pharmacology
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Biochemical Characterization of a Novel Channel-Activating Site on Nicotinic Acetylcholine Receptors

1993

We have studied the interaction of the reversible acetylcholine esterase inhibitor (-)physostigmine and several structurally related compounds with the nicotinic acetylcholine receptor (nAChR) from Torpedo marmorata electric tissue by means of ligand-induced ion flux into nAChR-rich membrane vesicles, direct binding studies and photoaffinity labeling. (-)Physostigmine acts as a channel-activating ligand at low concentrations and as a direct channel blocker at elevated concentrations. Channel activation is not inhibited by desensitizing concentrations of ACh or ACh-competitive ligands (including alpha-bungarotoxin and D-tubocurarine) but is inhibited by antibody FK1 and several other compoun…

PharmacologyPhotoaffinity labelingChemistryPhysostigmineMolecular Sequence DataIn Vitro TechniquesReceptors NicotinicTorpedoIon ChannelsAcetylcholine bindingNicotinic acetylcholine receptorNicotinic agonistnervous systemBiochemistrymedicineAnimalsChannel blockerAmino Acid SequenceBinding siteAcetylcholineAcetylcholine receptormedicine.drugJournal of Receptor Research
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Identification of Purine Binding Sites on Torpedo Acetylcholine Receptor

1994

Electrophysiological studies from this and other laboratories have suggested a direct action of ATP on nicotinic acetylcholine receptors (nAChR). To determine the site of binding of this purine derivative, we have covalently modified the nAChR from Torpedo marmorata electrocytes employing 2-[3H]-8-azido-ATP as a photoactivable affinity label. Covalently attached radioactivity was predominantly found in the beta-polypeptide of the receptor. Based on the results of protection studies with several nAChR ligands whose target sites at the receptor are known, we conclude that the purine site(s) differ from those of acetylcholine and of physostigmine, galanthamine and related ligands, and those of…

PharmacologyPurineAzidesBinding SitesbiologyChemistryAffinity labelAffinity LabelsReceptors NicotinicTorpedolaw.inventionchemistry.chemical_compoundAdenosine TriphosphateNicotinic agonistBiochemistrylawbiology.proteinmedicineAnimalsBinding siteReceptorTorpedoAcetylcholinemedicine.drugAcetylcholine receptorJournal of Receptor Research
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Biotin-Labelled and Photoactivatable Aldosterone and Progesterone Derivatives as Ligands for Affinity Chromatography, Fluorescence Immunoassays and P…

1996

New derivatives of progesterone and aldosterone were synthesized and functionally tested with commercially available antibodies. The covalent labelling of antibodies specific for aldosterone and progesterone was detected by SDS/PAGE analysis and subsequent autoradiography after using 3-(O-carboxymethyl)-oximino-(3-[125I]iodo-4-azidosalicylamidobu tylamine) derivatives of aldosterone and progesterone, respectively, as photoactivatable radioligands. Labelling was not observed in the presence of an excess of the unlabelled steroid. Aldosterone was labelled with biotin and used as a tracer in a time-resolved fluorescence immunoassay. The nonradioactive tracer is highly selective for its antibod…

Photochemistrymedicine.medical_treatmentAffinity labelBiotinFluorescent Antibody TechniqueLigandsBiochemistryAntibodiesChromatography AffinitySteroidchemistry.chemical_compoundBiotinAffinity chromatographyLabellingmedicineAnimalsAldosteroneProgesteroneAldosteroneChromatographyProgesterone CongenersPhotoaffinity labelingbiologyAffinity LabelsSerum Albumin BovinechemistryBiochemistryPolyclonal antibodiesbiology.proteinCattleEuropean Journal of Biochemistry
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Reducing the contribution of the photoemission process to the unwanted beam in photoelectron sources at accelerators

2017

Negative electron affinity (NEA) GaAs photocathodes show different pulse responses depending on the wavelength of photoexcitation. The pulse response at 800 nm shows a long and relatively intense tail, whereas at 400 nm, a tail of similar shape but with an intensity lower by around two orders of magnitude is observed. We explain this behavior with the specific properties of NEA photocathodes and compare it with the response of a positive electron affinity photocathode.

Physics and Astronomy (miscellaneous)ChemistryParticle accelerator02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesPhotocathodelaw.inventionGallium arsenidePhotoexcitationWavelengthchemistry.chemical_compoundlawElectron affinity0103 physical sciencesAtomic physics010306 general physics0210 nano-technologyBeam (structure)Order of magnitudeApplied Physics Letters
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PNO-CI and CEPA studies of electron correlation effects

1974

Ab initio calculations of the potential curves of low laying electronic states of OH are performed on the basis of a variational configuration interaction wavefunction (PNO-CI) and the coupled electron pair approximation (CEPA). The latter approach yields a ground state potential curve which deviates from the RKR curve by less than 200 cm−1 in the region from 0.7 to 1.6 A. Calculated ground state constants are as follows (experimental values in parentheses): r e = 0.972 (0.971) A, B e = 18.85 (18.87) cm−1, α e = 0.727 (0.714) cm−1, ω e = 3742 (3739) cm−1, ω e χ e = 85.3 (86.4) cm−1, μ0 = 1.686 (1.66) D, D e = 4.35 (4.63) eV,IP = 12.78 (13.36?) eV, El.Aff. = 1.51 (1.83) eV, v 00(2Π↔2Σ+) = 32…

PhysicsDipoleElectron pairElectronic correlationAb initio quantum chemistry methodsIonizationElectron affinityChiropracticsPhysical and Theoretical ChemistryConfiguration interactionAtomic physicsGround stateTheoretica Chimica Acta
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The electron affinity of phosphorus

2007

We have measured the energies of all three fine structure components in the 3PJ ground state of the negative ion of phosphorus using laser photodetachment threshold spectroscopy. The experiment yielded an electron affinity of 746.68(6) meV. The ΔJ = 2–0, 2–1 and 1–0 fine structure splittings were determined to be 32.73(7) meV, 22.48(7) meV and 10.25(3) meV, respectively. In the experiment, a mass selected beam of P− ions was merged with the output from a pulsed infrared optical parametric oscillator. The residual atoms produced in the photodetachment process were detected and used as a monitor of the photon-energy dependence of the relative cross section. The Wigner law was fitted to each o…

PhysicsInfraredCondensed Matter PhysicsLaserAtomic and Molecular Physics and Opticslaw.inventionIonlawElectron affinityOptical parametric oscillatorAtomic physicsGround stateSpectroscopyBeam (structure)Journal of Physics B: Atomic, Molecular and Optical Physics
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F-type lectin from serum of the Antarctic teleost fish Trematomus bernacchii (Boulenger, 1902): Purification, structural characterization, and bacter…

2021

Abstract The increasing availability of sequenced genomes has enabled a deeper understanding of the complexity of fish lectin repertoires involved in early development and immune recognition. The teleost fucose-type lectin (FTL) family includes proteins that preferentially bind fucose and display tandemly arrayed carbohydrate-recognition domains (CRDs) or are found in mosaic combinations with other domains. They function as opsonins, promoting phagocytosis and the clearance of microbial pathogens. The Antarctic fish Trematomus bernacchii is a Perciforme living at extremely low temperatures (−1.68 °C) which is considered a model for studying adaptability to the variability of environmental w…

PhysiologyAntarctic fishLectins F-type lectin Antarctic fish Trematomus bernacchii Bacterial agglutinationAntarctic RegionsTrematomus bernacchiiBiochemistryAntarctic fish; Bacterial agglutination; F-type lectin; Lectins; Trematomus bernacchii; Amino Acid Sequence; Animals; Antarctic Regions; Bacteria; Base Sequence; Fucose; Lectins; Perciformes; PhylogenyFucose03 medical and health scienceschemistry.chemical_compound0302 clinical medicineAffinity chromatographyWestern blotLectinsTrematomusmedicineAnimalsAmino Acid SequenceSea bassPerciformeMolecular BiologyOpsoninPhylogeny030304 developmental biologyFucoseAntarctic Region0303 health sciencesbiologyMolecular massmedicine.diagnostic_testBacteriaBase SequenceAnimalLectinBacterial agglutinationbiology.organism_classificationPerciformesBiochemistrychemistrybiology.proteinLectinF-type lectin030215 immunologyComparative biochemistry and physiology. Part B, Biochemistrymolecular biology
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Photoaffinity labeling of Torpedo acetylcholine receptor by physostigmine.

1993

The plant alkaloid physostigmine, an established anti-cholinesterase agent of the carbamate type, has recently been shown to bind to the nicotinic acetylcholine receptor from Torpedo marmorata electrocytes [Okonjo, K. O., Kuhlmann, J.Maelicke, A. (1991) Eur. J. Biochem. 200, 671-677]. Pharmacological studies of physostigmine-induced ion flux into nicotinic-acetylcholine-receptor-rich membrane vesicles, indicated distinct binding sites for physostigmine and acetylcholine. As shown in this study by photoaffinity labeling with [phenyl-(n)-3H](-)physostigmine, the physostigmine-binding site is located within the same subunit (alpha polypeptide) of the receptor as the acetylcholine-binding site.…

PhysostigmineStereochemistryPhotochemistryUltraviolet RaysPhysostigmineMolecular Sequence DataReceptors NicotinicTorpedoTritiumBiochemistrylaw.inventionlawmedicineAnimalsAmino Acid SequenceAcetylcholine receptorBinding SitesPhotoaffinity labelingChemistryAffinity LabelsBungarotoxinLigand (biochemistry)Nicotinic acetylcholine receptorBiochemistryTorpedoAcetylcholinemedicine.drugEuropean journal of biochemistry
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