Search results for "protein dynamics"

showing 10 items of 61 documents

Dynamic properties of some β-chain mutant hemoglobins

1995

The thermal behavior of the Soret band relative to the carbonmonoxy derivatives of some beta-chain mutant hemoglobins is studied in the temperature range 300-10 K and compared to that of wild-type carbonmonoxy hemoglobin. The band profile at various temperatures is modeled as a Voigt function that accounts for homogeneous broadening and for the coupling with high- and low-frequency vibrational modes, while inhomogeneous broadening is taken into account with a gaussian distribution of purely electronic transition frequencies. The various contributions to the over-all bandwidth are singled out with this analysis and their temperature dependence, in turn, gives information on structural and dy…

Voigt profileCoupling constantBase SequenceChemistryProtein dynamicsMolecular Sequence DataAnharmonicityHemoglobin AHemeBiochemistryRecombinant ProteinsMolecular electronic transitionCold TemperatureCrystallographyCarboxyhemoglobinModels ChemicalSpectrophotometryStructural BiologyMolecular vibrationMutationMutagenesis Site-DirectedHomogeneous broadeningRotational–vibrational couplingMolecular BiologyProteins: Structure, Function, and Genetics
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Computational Modeling of Protein Dynamics in Eukaryotic Cells

2012

Proteins have important functions inside the cell, traveling diffusively or being actively transported to various cellular sites where their activity is needed. Protein motion in the cellular environment is therefore an important topic to understand. However, the cell provides a very complex environment for that motion, which poses problems especially for any modeling effort designed to interpret experimentally observed features. So as to gain a realistic picture of protein dynamics inside the cell, we have recently introduced advanced numerical methods for describing that dynamics [1]. The starting point is an accurate numerical duplicate of the cell determined by LSCM, which can be used a…

Yellow fluorescent proteinbiologyChemistryProtein dynamicsNumerical analysisDynamics (mechanics)BiophysicsNanotechnologyPhotobleachingCytoplasmbiology.proteinDiffusion (business)Biological systemPorous mediumBiophysical Journal
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2015

Chemical ligation has been used to alter motions in specific regions of dihydrofolate reductase from E. coli and to investigate the effects of localized motional changes on enzyme catalysis. Two isotopic hybrids were prepared; one with the mobile N-terminal segment containing heavy isotopes (2H, 13C, 15N) and the remainder of the protein with natural isotopic abundance, and the other one with only the C-terminal segment isotopically labeled. Kinetic investigations indicated that isotopic substitution of the N-terminal segment affected only a physical step of catalysis, whereas the enzyme chemistry was affected by protein motions from the C-terminal segment. QM/MM studies support the idea th…

biologyStereochemistryChemistryProtein dynamicsNatural abundanceGeneral ChemistryCatalysisEnzyme catalysisCatalysisIntramolecular forceKinetic isotope effectDihydrofolate reductasebiology.proteinChemical ligationAngewandte Chemie International Edition
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Studying the role of protein dynamics in an SN2 enzyme reaction using free-energy surfaces and solvent coordinates

2013

Conformational changes are known to be able to drive an enzyme through its catalytic cycle, allowing, for example, substrate binding or product release. However, the influence of protein motions on the chemical step is a controversial issue. One proposal is that the simple equilibrium fluctuations incorporated into transition-state theory are insufficient to account for the catalytic effect of enzymes and that protein motions should be treated dynamically. Here, we propose the use of free-energy surfaces, obtained as a function of both a chemical coordinate and an environmental coordinate, as an efficient way to elucidate the role of protein structure and motions during the reaction. We sho…

chemistry.chemical_classificationFlexibility (engineering)Quantitative Biology::BiomoleculesChemistryQuantitative Biology::Molecular NetworksGeneral Chemical EngineeringProtein dynamicsProteinsGeneral ChemistryCatalysisQuantitative Biology::Subcellular ProcessesSolventCrystallographyEnzymeChemical physicsSolventsThermodynamicsSN2 reactionProteïnesEnergy (signal processing)
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The protein dynamical transition does not require the protein polypeptide chain

2011

We give experimental evidence that the main features of protein dynamics revealed by neutron scattering, i.e., the “protein dynamical transition” and the “boson peak”, do not need the protein polypeptide chain. We show that a rapid increase of hydrogen atoms fluctuations at about 220 K, analogous to the one observed in hydrated myoglobin powders, is also observed in a hydrated amino acids mixture with the chemical composition of myoglobin but lacking the polypeptide chain; in agreement with the protein behavior, the transition is abolished in the dry mixture. Further, an excess of low-frequency vibrational modes around 3 meV, typically observed in protein powders, is also observed in our mi…

chemistry.chemical_classificationHydrogenProtein dynamicsProtein mean square displacementchemistry.chemical_elementNeutron scatteringHydrated powdersInelastic neutron scatteringAmino acidAmino acidCrystallographychemistry.chemical_compoundchemistryMyoglobinMolecular vibrationSide chainProtein dynamicGeneral Materials ScienceElastic neutron scatteringPhysical and Theoretical ChemistryChemical composition
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On dynamics of parvoviral replication protein NS1

2010

fluorescent fusion proteinshelicasesATPasescanine parvovirusfluoresenssifuusioproteiinitphotobleachingATP bindinghelikaasitkoiran parvovirusATP-molekyylitprotein dynamicsfluorescent recoveryparvovirukset
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Hydration dependence of myoglobin dynamics studied with elastic neutron scattering, differential scanning calorimetry and broadband dielectric spectr…

2014

In this work we present a thorough investigation of the hydration dependence of myoglobin dynamics. The study is performed on D2O-hydrated protein powders in the hydration range 0<h<0.5 (h≡gr[D2O]/gr[protein]) and in the temperature range 20-300K. The protein equilibrium fluctuations are investigated with Elastic Neutron Scattering using the spectrometer IN13 at ILL (Grenoble), while the relaxations of the protein + hydration water system are investigated with Broadband Dielectric Spectroscopy; finally, Differential Scanning Calorimetry is used to obtain a thermodynamic description of the system. The effect of increasing hydration is to speed up the relaxations of the myoglobin + hydration …

inorganic chemicalsWork (thermodynamics)BiophysicsNeutron scatteringMolecular Dynamics SimulationBiochemistryPhase Transitionchemistry.chemical_compoundDifferential scanning calorimetryAnimalsHorsesRange (particle radiation)Calorimetry Differential ScanningMyoglobinProtein dynamicsOrganic ChemistryDynamics (mechanics)WaterSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)Neutron DiffractionMyoglobinchemistryChemical physicsDielectric SpectroscopyPhysical chemistryGlass transition•Protein dynamics •Equilibrium fluctuations •Protein/hydration water relaxations •Glass transition •Hydration water liquid-liquid transitionBiophysical chemistry
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Intranuclear dynamics in parvovirus infection

2009

koiran parvovirusfluorescent proteinssoluorganellitprotein dynamicscanine parvovirusdiffusion processesnuclear organellesimmunofluoresenssileimausfluoresoivat proteiinitproteiinien dynamiikkaparvovirukset
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Immobilization of proteins in silica gel: Biochemical and biophysical properties

2015

The development of silica-based sol-gel techniques compatible with the retention of protein structure and function started more than 20 years ago, mainly for the design of biotechnological devices or biomedical applications. Silica gels are optically transparent, exhibit good mechanical stability, are manufactured with different geometries, and are easily separated from the reaction media. Biomolecules encapsulated in silica gel normally retain their structural and functional properties, are stabilized with respect to chemical and physical insults, and can sometimes exhibit enhanced activity in comparison to the soluble form. This review briefly describes the chemistry of protein encapsulat…

protein dynamicsol-gel; encapsulation; biophysics; protein dynamics; heme proteinsOrganic Chemistrysol-gelencapsulationConformational transitionsProtein dynamicsbiophysicSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)heme proteins
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Investigating protein structure and dynamics through wide-angle X-ray solution scattering

2016

Wide-angle X-ray scattering (WAXS) is a powerful tool that can be used to gain information on the structure and dynamics of proteins and other biomolecules in solution. Improved methods for the calculation of WAXS patterns from available or putative protein models allow to better exploit the structural information contained in the experimental data. These methods, together with recent applications of static and time-resolved WAXS, are briefly reviewed.

protein dynamics conformational changes synchrotron x-felSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)
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