Search results for "Protein dynamic"

showing 10 items of 82 documents

Myoglobin embedded in saccharide amorphous matrices: water-dependent domains evidenced by small angle X-ray scattering

2010

We report Small Angle X-ray Scattering (SAXS) measurements performed on samples of carboxy-myoglobin (MbCO) embedded in low-water trehalose glasses. Results showed that, in such samples, "low-protein" trehalose-water domains are present, surrounded by a protein-trehalose-water background; such finding is supported by Infrared Spectroscopy (FTIR) measurements. These domains, which do not appear in the absence of the protein and in analogous sucrose systems, preferentially incorporate the incoming water at the onset of rehydration, and disappear following large hydration. This observation suggests that, in organisms under anhydrobiosis, analogous domains could play a buffering role against th…

Photosynthetic reaction centreSucroseGLASS-TRANSITIONGeneral Physics and AstronomyInfrared spectroscopyRhodobacter sphaeroideschemistry.chemical_compoundRhodobacter sphaeroidesScattering Small AngleSpectroscopy Fourier Transform InfraredPHOSPHOLIPID-BILAYERREACTION CENTERSPhysical and Theoretical ChemistrySettore CHIM/02 - Chimica FisicabiologyScatteringSmall-angle X-ray scatteringMyoglobinTrehaloseWaterbiology.organism_classificationPROTEIN DYNAMICSTrehaloseMOLECULAR-DYNAMICS SIMULATIONAmorphous solidCrystallographyMyoglobinchemistryTHERMAL-DENATURATIONNEUTRON-SCATTERINGCARBOXY-MYOGLOBINEXTERNAL MATRIXTREHALOSE-COATED MBCO
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Physical Origin of Anharmonic Dynamics in Proteins: New Insights From Resolution-Dependent Neutron Scattering on Homomeric Polypeptides

2012

Neutron scattering reveals a complex dynamics in polypeptide chains, with two main onsets of anharmonicity whose physical origin and biological role are still debated. In this study the dynamics of strategically selected homomeric polypeptides is investigated with elastic neutron scattering using different energy resolutions and compared with that of a real protein. Our data spotlight the dependence of anharmonic transition temperatures and fluctuation amplitudes on energy resolution, which we quantitatively explain in terms of a two-site model for the protein-hydration water energy landscape. Experimental data strongly suggest that the protein dynamical transition is not a mere resolution …

PhysicsQuantitative Biology::BiomoleculesfluctuationsResolution (electron density)AnharmonicityProtein dynamical transitionProteinsGeneral Physics and AstronomyNeutron scatteringMolecular physicsPhase TransitionSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)Neutron DiffractionComplex dynamicsAmplitudeModels ChemicalBiophysicsHomomericProtein dynamicConnection (algebraic framework)PeptidesEnergy (signal processing)
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The impact of high hydrostatic pressure on structure and dynamics of beta-lactoglobulin

2013

Abstract Methods Combining small-angle X-ray and neutron scattering measurements with inelastic neutron scattering experiments, we investigated the impact of high hydrostatic pressure on the structure and dynamics of β-lactoglobulin (βLG) in aqueous solution. Background βLG is a relatively small protein, which is predominantly dimeric in physiological conditions, but dissociates to monomer below about pH 3. Results High-pressure structural results show that the dimer–monomer equilibrium, as well as the protein–protein interactions, are only slightly perturbed by pressure, and βLG unfolding is observed above a threshold value of 3000 bar. In the same range of pressure, dynamical results put …

Protein ConformationHydrostatic pressureBiophysics02 engineering and technologyLactoglobulinsProtein dynamicsNeutron scatteringNeutron scattering010402 general chemistry01 natural sciencesBiochemistryInelastic neutron scatteringchemistry.chemical_compound[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyProtein foldingMolecular BiologyHydrostatic pressureQuantitative Biology::BiomoleculesAqueous solutionSmall angle X-ray and neutron scatteringProtein dynamics021001 nanoscience & nanotechnology0104 chemical sciencesCrystallographyMonomerchemistryChemical physicsCompressibilityProtein folding0210 nano-technology
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Conformational substates and dynamic properties of carbonmonoxy hemoglobin.

2003

Heme pocket dynamics of human carbonmonoxy hemoglobin (HbCO) is studied by Fourier transform infrared spectroscopy. The CO stretching band at various temperatures in the interval 300-10 K is analyzed in terms of three taxonomic A substates; however, in HbCO the band attributed to the A(1) taxonomic substate accounts for approximately 90% of the total intensity in the pH range 8.8-4.5. Two different regimes as a function of temperature are observed: below 160 K, the peak frequency and the bandwidth of the A(1) band have constant values whereas, above this temperature, a linear temperature dependence is observed, suggesting the occurrence of transitions between statistical substates within th…

Protein ConformationProtein dynamicsOrganic ChemistryAnharmonicityBiophysicsAnalytical chemistryTemperatureHemeHydrogen-Ion ConcentrationLigandsBiochemistryAmidesSolventchemistry.chemical_compoundCrystallographychemistryCarboxyhemoglobinAmideSpectroscopy Fourier Transform InfraredSolventsHumansHemoglobinFourier transform infrared spectroscopyGlass transitionHemeBiophysical chemistry
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Conformation and concerted dynamics of the integrin-binding site and the C-terminal region of echistatin revealed by homonuclear NMR

2005

Copyright © by Portland Press. The final version of record is available at http://www.biochemj.org/bj/default.htm

Protein ConformationStereochemistryIntegrinNMR protein dynamics determinationTripeptideBiochemistryHomonuclear moleculeOff-resonance rotating-frame Overhauser enhancement spectroscopy (off-resonance ROESY)Protein structureSide chainAnimalsNuclear Magnetic Resonance BiomolecularMolecular BiologyIntegrin bindingRGD motifchemistry.chemical_classificationBinding Sites:CIENCIAS DE LA VIDA::Bioquímica [UNESCO]ChemistryEchistatin integrinSnakesUNESCO::CIENCIAS DE LA VIDA::BioquímicaCell BiologyRGD disintegrin; Echistatin; Integrin; NMR protein dynamics determination; Off-resonance rotating-frame Overhauser enhancement spectroscopy (off-resonance ROESY)Protein Structure TertiaryAmino acidRGD disintegrinDocking (molecular)EchistatinIntercellular Signaling Peptides and ProteinsPeptidesResearch ArticleProtein Binding
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Insights into amyloid fibrils dynamics from neutron scattering

2011

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Protein dynamics Aggregation concanavalin A
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Neutron Scattering Reveals Enhanced Protein Dynamics in Concanavalin A Amyloid Fibrils

2012

Protein aggregation is one of the most challenging topics in life sciences, and it is implicated in several human pathologies. The nature and the role of toxic species is highly debated, with amyloid fibrils being among the most relevant species for their peculiar structural and functional properties. Protein dynamics and in particular the ability to fluctuate through a large number of conformational substates are closely related to protein function. This Letter focuses on amyloid fibril dynamics, and, to our knowledge, it is the first neutron scattering study on a protein (Concanavalin A) isolated in its fibril state. Our results reveal enhanced atomic fluctuations in amyloid fibrils and i…

Protein functionbiologyChemistryProtein dynamicsmean square displacementsA proteinatomic fluctuationsmacromolecular substancesProtein aggregationNeutron scatteringFibrilAmyloid fibrilatomic fluctuationprotein aggregationCrystallographyConcanavalin ABiophysicsbiology.proteinGeneral Materials SciencePhysical and Theoretical Chemistry
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Inter- and intramolecular motions in proteins

1992

The use of 57 Fe Mossbauer radiation allows the study of protein crystal dynamics by a time-resolved analysis of X-ray scattering. In myoglobin crystals, the main source of the root mean squared amplitude of motions come from intramolecular protein dynamics. Segments of the size of an α-helix move collectively. Long-range correlated motions give only a minor contribution. Comparison with Mossbauer absorption spectroscopy shows that protein-specific dynamics is frozaen out below 200 K and the lattice dynamics in mainly responsible for the low-temperature behavior

Quantitative Biology::BiomoleculesAbsorption spectroscopyScatteringProtein dynamicsCondensed Matter PhysicsAtomic and Molecular Physics and OpticsRoot mean squarechemistry.chemical_compoundAmplitudeNuclear magnetic resonanceMyoglobinchemistryChemical physicsIntramolecular forcePhysical and Theoretical ChemistryProtein crystallizationInternational Journal of Quantum Chemistry
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Incoherent elastic and quasi-elastic neutron scattering investigation of hemoglobin dynamics.

2005

In this work we investigate the dynamic properties of hemoglobin in glycerolD(8)/D(2)O solution using incoherent elastic (ENS) and quasi-elastic (QENS) neutron scattering. Taking advantage of complementary energy resolutions of backscattering spectrometers at ILL (Grenoble), we explore motions in a large space-time window, up to 1 ns and 14 A; moreover, in order to cover the harmonic and anharmonic protein dynamics regimes, the elastic experiments have been performed over the wide temperature interval of 20-300 K. To study the dependence of the measured dynamics upon the protein quaternary structure, both deoxyhemoglobin (in T quaternary conformation) and carbonmonoxyhemoglobin (in R quater…

Quantitative Biology::BiomoleculesChemistryProtein dynamicsOrganic ChemistryNeutron diffractionMomentum transferAnharmonicityBiophysicsTemperatureProtein dynamicsHemoglobin quaternary structureMean square displacementDynamical transitionNeutron scatteringBiochemistryElasticityMean squared displacementOxygenHemoglobinsNeutron DiffractionHumansDiffusion (business)Atomic physicsStructure factorHydrogenBiophysical chemistry
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A benchmark for protein dynamics: Ribonuclease A measured by neutron scattering in a large wavevector-energy transfer range

2008

The dynamics of Ribonuclease A was explored in the full range of time and length-scales accessible by neutron spectroscopy, on time-of-flight, backscattering and spin-echo spectrometers. Samples were examined in dry and hydrated powder forms and in concentrated and dilute solutions. The aim of the study was an experimental characterisation of the full variety of protein dynamics arising from stabilisation forces. The results provide a benchmark against which other sample dynamics can be compared.

Quantitative Biology::BiomoleculesRange (particle radiation)SpectrometerChemistryProtein dynamicsDynamics (mechanics)General Physics and AstronomyNeutron scatteringMolecular physicsNeutron spectroscopyBenchmark (computing)Wave vectorPhysical and Theoretical ChemistryAtomic physicsChemical Physics
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