Search results for "hemocyanin"

showing 10 items of 148 documents

Keyhole limpet hemocyanin (KLH), I: Reassociation from Immucothel® followed by separation of KLH1 and KLH2

1997

Abstract Studies of keyhole limpet hemocyanin (KLH) normally require purification of functional complexes directly from living animals. An alternative procedure is described wherein a commercial preparation of KLH which is fully dissociated into its subunits (Immucothel®, biosyn Arzneimittel GmbH) is reassociated in the presence of a high concentration of calcium and magnesium. The reassociation products, when observed by electron microscopy, consist of didecamers, multidecamers and flexible tubules of varying length. The two forms of KLH described previously and designated KLH1 and KLH2, are present in the reassocated mixture as homo-oligomers/polymers and can be separated by selective dis…

ChromatographybiologyMacromolecular SubstancesElutionProtein subunitSize-exclusion chromatographyGeneral Physics and AstronomyCell BiologyMegathura crenulatabiology.organism_classificationNegative stainRespiratory proteinMicroscopy ElectronMolluscaStructural BiologyHemocyaninsPEG ratioChromatography Gelbiology.proteinAnimalsIndicators and ReagentsGeneral Materials ScienceCrystallizationKeyhole limpet hemocyaninMicron
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Molecular heterogeneity of the hemocyanin isolated from the king crabParalithodes camtschaticae

2000

Native Paralithodes camtschaticae hemocyanin is found as a mixture of dodecamers (24S; 80%) and hexamers (16S; 20%). Removal of Ca2+ ions by dialysis against EDTA-containing buffer solution at neutral pH induces complete dissociation of the 24S form into the 16S form. Under these conditions, a further increase in pH to 9.2 produces complete dissociation of the hexamers into monomers (5S). In both cases, the dissociation process is reversible. The dodecamer (24S) is composed of two different hexamers which can be discriminated only by ion-exchange chromatography in the presence of Ca2+ ions. At alkaline pH and in the presence of EDTA, two major monomeric fractions can be separated by ion-exc…

Chromatographymedicine.medical_treatmentHemocyaninBohr effectBuffer solutionBiochemistryDissociation (chemistry)Crystallographychemistry.chemical_compoundDodecameric proteinMonomerchemistrymedicineProtein quaternary structureOxygen bindingEuropean Journal of Biochemistry
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The Allosteric Effector l-Lactate Induces a Conformational Change of 2×6-meric Lobster Hemocyanin in the Oxy State as Revealed by Small Angle X-ray S…

2001

Abstract Hemocyanins are multisubunit respiratory proteins found in many invertebrates. They bind oxygen highly cooperatively. However, not much is known about the structural basis of this behavior. We studied the influence of the physiological allosteric effectorl-lactate on the oxygenated quaternary structure of the 2×6-meric hemocyanin from the lobster Homarus americanus employing small angle x-ray scattering (SAXS). The presence of 20 mm l-lactate resulted in different scattering curves compared with those obtained in the absence of l-lactate. The distance distribution functionsp(r) indicated a more compact molecule in presence ofl-lactate, which is also reflected in a reduction of the …

Conformational changeProtein ConformationScatteringChemistrySmall-angle X-ray scatteringmedicine.medical_treatmentAllosteric regulationHemocyaninCell BiologyBiochemistryNephropidaeMicroscopy ElectronCrystallographyAllosteric RegulationHemocyaninsRadius of gyrationmedicineAnimalsScattering RadiationProtein quaternary structureLactic AcidMolecular BiologyOxygen bindingJournal of Biological Chemistry
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Small-angle neutron scattering reveals an oxygen-dependent conformational change of the immunogen keyhole limpet hemocyanin type 1 (KLH1).

2001

The respiratory protein of the keyhole limpet, Megathura crenulata, the hemocyanin (KLH), commonly used as an immunogen, binds oxygen cooperatively, which implies the existence of different conformations. For the first time, two different conformations of KLH1 were detected upon oxygenation, a deoxy and an oxy state, using small-angle neutron scattering. Rearrangements in the quaternary structure of KLH1 were predicted from the different radii of gyration and the shifts of the minima and maxima in the scattering curves. Upon oxygenation, KLH1 becomes smaller and more compact. Model reconstruction of KLH1 indicates a hollow cylinder with two rings located close to both ends, which move sligh…

Conformational changeProtein Conformationmedicine.medical_treatmentBiophysicsNeutron scatteringMegathura crenulataBiophysical PhenomenamedicineAnimalsScattering RadiationProtein Structure QuaternaryNeutronsbiologyChemistryScatteringHemocyaninGeneral Medicinebiology.organism_classificationSmall-angle neutron scatteringRespiratory proteinOxygenCrystallographyMolluscaHemocyaninsbiology.proteinKeyhole limpet hemocyaninProtein BindingEuropean biophysics journal : EBJ
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Hemocyanin conformational changes associated with SDS-induced phenol oxidase activation.

2007

The enzymatic activity of phenoloxidase is assayed routinely in the presence of SDS. Similar assay conditions elicit phenoloxidase activity in another type 3 copper protein, namely hemocyanin, which normally functions as an oxygen carrier. The nature of the conformational changes induced in type 3 copper proteins by the denaturant SDS is unknown. This comparative study demonstrates that arthropod hemocyanins can be converted from being an oxygen carrier to a form which exhibits phenoloxidase activity by incubation with SDS, with accompanying changes in secondary and tertiary structure. Structural characterisation, using various biophysical methods, suggests that the micellar form of SDS is …

Copper proteinmedicine.medical_treatmentBiophysicschemistry.chemical_elementBiochemistryOxygenProtein Structure SecondaryAnalytical ChemistryScorpionsEnzyme activatorCatalytic DomainHorseshoe CrabsmedicineAnimalsMolecular Biologychemistry.chemical_classificationOxidase testMonophenol MonooxygenaseSodium Dodecyl SulfateHemocyaninIsothermal titration calorimetrySpidersProtein tertiary structureProtein Structure TertiaryEnzyme ActivationEnzymechemistryBiochemistryHemocyaninsCopperBiochimica et biophysica acta
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Functional Changes in the Family of Type 3 Copper Proteins During Evolution

2004

Copper proteinmedicine.medical_treatmentCopper metabolismchemistry.chemical_elementMoltingBiologyBiochemistryEvolution MolecularMolecular evolutionMetalloproteinmedicineAnimalsMolecular Biologychemistry.chemical_classificationWound HealingMonophenol MonooxygenaseOrganic ChemistryHemocyaninGeneral MedicineCopperBiochemistrychemistryMonophenol monooxygenaseHemocyaninsImmunologyMolecular MedicineCopperChemBioChem
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8 Å cryo-TEM and single particle analysis of Nautilus pompilius hemocyanin under two states of oxygenation

2007

Extended abstract of a paper presented at MC 2007, 33rd DGE Conference in Saarbrücken, Germany, September 2 – September 7, 2007

Cryo temMaterials sciencebiologymedicine.medical_treatmentmedicineBiophysicsSingle particle analysisHemocyaninOxygenationNautilusbiology.organism_classificationInstrumentationMicroscopy and Microanalysis
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3-D reconstruction of hemocyanins and other invertebrate hemolymph proteins by cryo-TEM: an overview.

2004

Cryoelectron MicroscopyGeneral Physics and AstronomyCell BiologyAnatomyBiologyCryo temBiochemistryStructural BiologyHemolymphHemolymphHemocyaninsAnimalsGeneral Materials ScienceInvertebrateMicron (Oxford, England : 1993)
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Quaternary structure and molecular model of a 4x6mer arthropod hemocyanin in oxygenated and deoxygenated states by 3D cryo-electron microscopy

2007

Extended abstract of a paper presented at MC 2007, 33rd DGE Conference in Saarbrücken, Germany, September 2 – September 7, 2007

CrystallographyMolecular modelbiologyChemistryCryo-electron microscopymedicine.medical_treatmentBiophysicsmedicineProtein quaternary structureHemocyaninArthropodbiology.organism_classificationInstrumentationMicroscopy and Microanalysis
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Influence of Temperature, Hypercapnia, and Development on the Relative Expression of Different Hemocyanin Isoforms in the Common CuttlefishSepia offi…

2012

The cuttlefish Sepia officinalis expresses several hemocyanin isoforms with potentially different pH optima, indicating their reliance on efficient pH regulation in the blood. Ongoing ocean warming and acidification could influence the oxygen-binding properties of respiratory pigments in ectothermic marine invertebrates. This study examined whether S. officinalis differentially expresses individual hemocyanin isoforms to maintain optimal oxygen transport during development and acclimation to elevated seawater pCO2 and temperature. Using quantitative PCR, we measured relative mRNA expression levels of three different hemocyanin isoforms in several ontogenetic stages (embryos, hatchlings, juv…

Cuttlefish0303 health sciencesPhysiologyEcology030310 physiologyOntogenymedicine.medical_treatmentOxygen transportHemocyaninMarine invertebratesBiologybiology.organism_classificationCephalopod03 medical and health sciencesBiochemistryHemolymphGeneticsmedicineAnimal Science and Zoology14. Life underwaterSepiaMolecular BiologyEcology Evolution Behavior and Systematics030304 developmental biologyJournal of Experimental Zoology Part A: Ecological Genetics and Physiology
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