Search results for "Myoglobin"

showing 10 items of 141 documents

Elastic neutron scattering of dry and rehydrated trehalose coated carboxy-myoglobin

2008

We report here a comparison between the hydrogen atoms mean square displacements measured by elastic neutron scattering on trehalose coated carboxy-myoglobin, at ILL on the backscattering spectrometers IN13 and IN16. An inconsistency is observed when comparing the mean square displacements measured on the two spectrometer, on samples of identical composition, since they resulted of larger amplitude on IN13 (either in condition of drought or after overnight rehydration under 75% D2O atmosphere), notwithstanding the lower time window accessible on this instrument with respect to IN16. Such inconsistency disappears when the data obtained on this last spectrometer are analyzed in two separate r…

SpectrometerHydrogenChemistryEnthalpyAnalytical chemistryPROTEINGeneral Physics and Astronomychemistry.chemical_elementNeutron scatteringMOLECULAR-DYNAMICS SIMULATIONTrehalosechemistry.chemical_compoundROOM-TEMPERATUREAmplitudeMyoglobinWATEREXTERNAL MATRIXWave vectorPhysical and Theoretical Chemistryneutron-scattering trehalose myoglobin
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A comparative study of carboxy myoglobin in saccharide-water systems by molecular dynamics simulation.

2007

Results from room-temperature molecular dynamics simulation on a system containing carboxy-myoglobin, water, and maltose molecules are reported. Protein atomic fluctuations, protein−solvent and solvent−solvent hydrogen bonding have been analyzed and compared to the ones in trehalose−water and sucrose−water systems (Proteins 2005, 59, 291−302). Results help in rationalizing, at a molecular level, the effects of homologues disaccharides on protein structure/dynamics experimentally observed. Furthermore, the effectiveness of disaccharides in bioprotection in terms of peculiar protein−matrix coupling is also discussed.

SucroseHydrogen bondMyoglobinmyoglobin simulation conformational substates disaccharideTrehaloseWaterHydrogen BondingMaltoseSurfaces Coatings and FilmsProtein Structure Tertiarychemistry.chemical_compoundMolecular dynamicsProtein structureMolecular levelchemistryMyoglobinModels ChemicalComputational chemistryMaterials ChemistryMoleculeComputer SimulationPhysical and Theoretical ChemistryMaltoseThe journal of physical chemistry. B
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Dehydration and crystallization of trehalose and sucrose glasses containing carbonmonoxy-myoglobin

1999

We report a study wherein we contemporarily measured 1) the dehydration process of trehalose or sucrose glasses embedding carbonmonoxy-myoglobin (MbCO) and 2) the evolution of the A substates in saccharide-coated MbCO. Our results indicate that microcrystallization processes, sizeably different in the two saccharides, take place during dehydration; moreover, the microcrystalline structure is maintained unless the dry samples are equilibrated with a humidity >/=75% (>/=60%) at 25 degrees C for the trehalose (sucrose) sample. The evolution of the parameters that characterize the A substates of MbCO indicates that 1) the effects of water withdrawal are analogous in samples dried in the presenc…

SucroseSucrosePopulationBiophysicsBiophysical Phenomenalaw.inventionchemistry.chemical_compoundlawSpectroscopy Fourier Transform InfraredmedicineAnimalsHorsesDehydrationDesiccationCrystallizationSugareducationeducation.field_of_studyMyoglobinTrehaloseHumiditymedicine.diseaseTrehaloseCrystallographyMicrocrystallinechemistryMyoglobinCrystallizationResearch Article
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“Water Association” Band in Saccharide Amorphous Matrices: Role of Residual Water on Bioprotection

2021

Saccharides protect biostructures against adverse environmental conditions mainly by preventing large scale motions leading to unfolding. The efficiency of this molecular mechanism, which is higher in trehalose with respect to other sugars, strongly depends on hydration and sugar/protein ratio. Here we report an Infrared Spectroscopy study on dry amorphous matrices of the disaccharides trehalose, maltose, sucrose and lactose, and the trisaccharide raffinose. Samples with and without embedded protein (Myoglobin) are investigated at different sugar/protein ratios, and compared. To inspect matrix properties we analyse the Water Association Band (WAB), and carefully decompose it into sub-bands,…

SucroseSucrosePopulationwaterLactose010402 general chemistry01 natural sciencesCatalysisArticleInorganic Chemistrylcsh:Chemistrychemistry.chemical_compoundRaffinose0103 physical sciencesAnimalsTrisaccharideHorsesPhysical and Theoretical ChemistryRaffinoseLactoseeducationSugarinfrared spectroscopyMolecular Biologylcsh:QH301-705.5Spectroscopytrehalosechemistry.chemical_classificationeducation.field_of_study010304 chemical physicsOrganic ChemistryGeneral MedicineMaltoseTrehalose0104 chemical sciencesComputer Science ApplicationschemistryChemical engineeringlcsh:Biology (General)lcsh:QD1-999myoglobinbiopreservation
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Calorimetric study of myoglobin embedded in trehalose-water matrixes

2009

It has been suggested that in ‘dry’ protein–trehalose–water systems, water–mediated hydrogen bond network, whose strength increases by drying, anchors the protein to its surroundings. To further characterize this effect, we performed a DSC study on low-water myoglobin–trehalose systems. The denaturation temperature resulted to increase by decreasing hydration, and linearly correlated to the glass transition temperature of both the ternary protein–water–trehalose and the binary water–trehalose systems. Further measurements are being performed to investigate eventual differences among different saccharides.

Ternary numeral systemChemistryHydrogen bondMineralogyCondensed Matter Physicschemistry.chemical_compoundDifferential scanning calorimetryChemical engineeringMyoglobinDenaturation (biochemistry)Physical and Theoretical ChemistryGlass transitionTernary operationThermal analysisdenaturation DSC glass transition myoglobin trehaloseJournal of Thermal Analysis and Calorimetry
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Protein dynamics observed by tunable mid-IR quantum cascade lasers across the time range from 10 ns to 1 s

2017

We have developed a spectrometer based on tunable quantum cascade lasers (QCLs) for recording time-resolved absorption spectra of proteins in the mid-infrared range. We illustrate its performance by recording time-resolved difference spectra of bacteriorhodopsin in the carboxylic range (1800–1700 cm− 1) and on the CO rebinding reaction of myoglobin (1960–1840 cm− 1), at a spectral resolution of 1 cm− 1. The spectrometric setup covers the time range from 4 ns to nearly a second with a response time of 10–15 ns. Absorption changes as low as 1 × 10− 4 are detected in single-shot experiments at t > 1 μs, and of 5 × 10− 6 in kinetics obtained after averaging 100 shots. While previous time-res…

Time FactorsSpectrophotometry InfraredAbsorption spectroscopyAnalytical chemistry010402 general chemistry53001 natural sciencesMolecular physicsSpectral lineAnalytical Chemistrylaw.inventionchannelrhodopsinflash photolysislawSpectral resolutionAbsorption (electromagnetic radiation)InstrumentationSpectroscopyCarbon MonoxidebiologySpectrometerChemistrybacteriorhodopsinLasers010401 analytical chemistry500 Naturwissenschaften und Mathematik::530 Physik::530 PhysikWaterBacteriorhodopsinLasertime-resolved IR spectroscopyAtomic and Molecular Physics and Optics0104 chemical sciencesSolutionsKineticsCascadeBacteriorhodopsinsmyoglobinbiology.proteinQuantum Theory
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Protein dynamics: conformational disorder, vibrational coupling and anharmonicity in deoxy-hemoglobin and myoglobin.

1993

In this work we study the temperature dependence of the Soret band lineshape of deoxymyoglobin and deoxyhemoglobin, in the range 300-20 K. To fit the measured spectra we use an approach originally proposed by Champion and coworkers (Srajer et al. 1986; Srajer and Champion 1991). The band profile is modelled as a Voigt function that accounts for the coupling with low frequency vibrational modes, whereas the coupling with high frequency modes is responsible for the vibronic structure of the spectra. Moreover, owing to the position of the iron atom out of the mean heme plane, inhomogeneous broadening brings about a non-Gaussian distribution of 0-0 electronic transition frequencies. The reporte…

Voigt profileChemical PhenomenaChemistry PhysicalMyoglobinProtein ConformationProtein dynamicsAnharmonicityBiophysicsTemperatureDynamic properties Heme proteins Optical spectroscopyGeneral MedicineMolecular physicsMolecular electronic transitionSpectral linechemistry.chemical_compoundHemoglobinsNuclear magnetic resonanceMyoglobinchemistrySpectrophotometryMolecular vibrationAnimalsThermodynamicsRotational–vibrational couplingEuropean biophysics journal : EBJ
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Structure-dynamics-function relationships in Asian elephant (Elephas maximus) myoglobin. An optical spectroscopy and flash photolysis study on functi…

1993

In this work we report the thermal behavior (10–300 K) of the Soret band lineshape of deoxy and carbonmonoxy derivatives of Asian elephant (Elephas maximus) and horse myoglobins together with their carbon monoxide recombination kinetics after flash photolysis; the results are compared to analogous data relative to sperm whale myoglobin. The Soret band profile is modeled as a Voigt function that accounts for the coupling with high and low frequency vibrational modes, while inhomogeneous broadening is taken into account with suitable distributions of purely electronic transition frequencies. This analysis makes it possible to isolate the various contributions to the overall lineshape that; in…

Voigt profilePhotolysisMyoglobinProtein ConformationPhotodissociationElephantsAnalytical chemistryElectron Spin Resonance SpectroscopyBiophysicsSoft modesMolecular electronic transitionchemistry.chemical_compoundStructure-Activity RelationshipMyoglobinchemistryCarboxyhemoglobinChemical physicsSpectrophotometryMolecular vibrationFlash photolysisAnimalsThermodynamicsHorsesSpectroscopyResearch ArticleBiophysical Journal
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Function and evolution of vertebrate globins.

2014

Globins are haem-proteins that bind O2 and thus play an important role in the animal's respiration and oxidative energy production. However, globins may also have other functions such as the decomposition or production of NO, the detoxification of reactive oxygen species or intracellular signalling. In addition to the well-investigated haemoglobins and myoglobins, genome sequence analyses have led to the identification of six further globin types in vertebrates: androglobin, cytoglobin, globin E, globin X, globin Y and neuroglobin. Here, we review the present state of knowledge on the functions, the taxonomic distribution and evolution of vertebrate globins, drawing conclusions about the fu…

Whole genome sequencingbiologyPhysiologyCytoglobinVertebrateOxidative phosphorylationAnatomyAdaptation PhysiologicalGlobinsEvolution Molecularchemistry.chemical_compoundMyoglobinchemistryEvolutionary biologyhemic and lymphatic diseasesbiology.animalNeuroglobinAnimalsHumansGlobinFunction (biology)PhylogenyActa physiologica (Oxford, England)
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Selective protein removal and desalting using microchip CE.

2006

Abstract This paper describes the on-line sample pretreatment and analysis of proteins and peptides with a poly(methylmethacrylate) (PMMA) microfluidic device (IonChip™). This chip consists of two hyphenated electrophoresis channels with integrated conductivity detectors. The first channel can be used for sample preconcentration and sample clean-up, while in the second channel the selected compounds are separated. Isotachophoresis (ITP) combined with zone electrophoresis (CZE) was used to preconcentrate a myoglobin sample by a factor of about 65 before injection into the second dimension and to desalt a mixture of six proteins with 100 mM NaCl. However, ITP–CZE could not be used for the rem…

chemistry.chemical_classificationChromatographyChemistryClinical BiochemistryMicrofluidicsAnalytical chemistryA proteinProteinsPeptideCell BiologyGeneral MedicineBiochemistrySample (graphics)Online SystemsAnalytical ChemistryElectrophoresis Microchipchemistry.chemical_compoundElectrophoresisMyoglobinAnimalsHumansIsotachophoresisJournal of chromatography. B, Analytical technologies in the biomedical and life sciences
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