Search results for "Biomolecule"

showing 10 items of 666 documents

Infrared bandshapes of intramolecularly H-bonded systems—III. Vibrational dephasing of vs (OH) in 2,6-dichlorophenol

1987

Abstract The shape of the v s (OH) absorption band of intramolecularly H-bonded 2,6-dichlorophenol was measured in a series of solvents of increasing polarity and quantitatively analyzed. A distinct dependence of band positions, shape parameters, band moments, integrated intensities, correlation functions and correlation times on the polarity of solvent has been found. Vibrational dephasing due to dipole—dipole interactions seems to be an important relaxation pathway determining the bandshape in the studied systems.

Quantitative Biology::Biomolecules26-DichlorophenolPolarity (physics)ChemistryInfraredDephasingRelaxation (NMR)General EngineeringSolventchemistry.chemical_compoundNuclear magnetic resonanceAbsorption bandPhysical chemistryPhysics::Chemical PhysicsSolvent effectsSpectrochimica Acta Part A: Molecular Spectroscopy
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The importance of vibronic perturbations in ferrocytochrome c spectra: a reevaluation of spectral properties based on low-temperature optical absorpt…

2005

We have measured and analyzed the low-temperature (T=10 K) absorption spectrum of reduced horse heart and yeast cytochrome c. Both spectra show split and asymmetric Q(0) and Q(upsilon) bands. The spectra were first decomposed into the individual split vibronic sidebands assignable to B(1g) (nu15) and A(2g) (nu19, nu21, and nu22) Herzberg-Teller active modes due to their strong intensity in resonance Raman spectra acquired with Q(0) and Q(upsilon) excitations. The measured band splittings and asymmetries cannot be rationalized solely in terms of electronic perturbations of the heme macrocycle. On the contrary, they clearly point to the importance of considering not only electronic perturbati…

Quantitative Biology::BiomoleculesAbsorption spectroscopyChemistryGeneral Physics and AstronomySpectral linesymbols.namesakeMolecular dynamicsElectric fieldExcited statesymbolsVibronic spectroscopyPhysical and Theoretical ChemistryAtomic physicsRaman spectroscopyLuminescenceThe Journal of chemical physics
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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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A nanodosimetric model of radiation-induced clustered DNA damage yields

2010

International audience; We present a nanodosimetric model for predicting the yield of double strand breaks (DSBs) and non-DSB clustered damages induced in irradiated DNA. The model uses experimental ionization cluster size distributions measured in a gas model by an ion counting nanodosimeter or, alternatively, distributions simulated by a Monte Carlo track structure code developed to simulate the nanodosimeter. The model is based on a straightforward combinatorial approach translating ionizations, as measured or simulated in a sensitive gas volume, to lesions in a DNA segment of one-two helical turns considered equivalent to the sensitive volume of the nanodosimeter. The two model paramete…

Quantitative Biology::BiomoleculesAlgorithms Computer Simulation DNA/*radiation effects DNA Breaks[PHYS.PHYS.PHYS-MED-PH] Physics [physics]/Physics [physics]/Medical Physics [physics.med-ph][ PHYS.PHYS.PHYS-MED-PH ] Physics [physics]/Physics [physics]/Medical Physics [physics.med-ph]Genetic Monte Carlo Method Nanotechnology/instrumentation/*methods Plasmids/radiation effects Probability Protons/adverse effects Radiometry/instrumentation/*methods Reproducibility of Results Saccharomyces cerevisiae SoftwareDouble-Stranded/radiation effects DNA Damage/*radiation effects Helium/adverse effects *Models
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A theoretical study of solvent effects on the conformational equilibria of neutral glycine in aqueous solution

2003

Abstract In this work conformational equilibrium of neutral glycine in solution is systematically investigated by using DFT and MP2 methods combined with solvent continuum models. A systematic exploration of the potential energy surface and full geometry optimizations for several conformers have been carried out in the gas phase and aqueous solution at the MP2/6-31+G** and B3LYP/6-31+G** levels. Zero-point and thermal contributions to the free energy have been obtained at the B3LYP level. Both theoretical levels lead to very similar results, in geometrical and energetic terms, both in the gas phase and in solution. Solvent effects play an important role on the conformational equilibria of n…

Quantitative Biology::BiomoleculesAqueous solutionChemistryCondensed Matter PhysicsBiochemistryTautomerSolventEnergy minimumComputational chemistryPotential energy surfaceThermalPhysics::Atomic and Molecular ClustersPhysics::Chemical PhysicsPhysical and Theoretical ChemistrySolvent effectsConformational isomerismJournal of Molecular Structure: THEOCHEM
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Amino Acid Chemistry in Solution:  Structural Study and Vibrational Dynamics of Glutamine in Solution. An ab Initio Reaction Field Model

1998

The self-consistent reaction field (SCRF) theory was used to study structural and vibrational features of the amino acid L-glutamine in solution. Raman and infrared spectra of this molecule in solutions of H 2O and D2O were recorded and measured. The bands were firstly assigned on the basis of the isotopic shifts. An ab initio quadratic force field at the 6-31 +G* level was achieved. The calculation simulated a polar solvent by placing the molecule in an ellipsoidal cavity surrounded by a continuum dielectric. The theoretical results, in terms of structural parameters, vibrational frequencies and descriptions, and infrared intensities, were in satisfactory agreement with the experimental da…

Quantitative Biology::BiomoleculesAqueous solutionChemistryIntermolecular forceAb initioInfrared spectroscopySurfaces Coatings and FilmsComputational chemistryNormal modeChemical physicsPolarizabilityMaterials ChemistryMoleculePhysics::Chemical PhysicsPhysical and Theoretical ChemistrySolvent effectsThe Journal of Physical Chemistry B
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Internal Rotation in Propionic Acid:  Near-Infrared-Induced Isomerization in Solid Argon

2005

The conformational system of propionic acid (CH3CH2COOH) is studied in solid argon. It is predicted by the ab initio calculations that this molecule has four stable conformers. These four structures are denoted Tt, Tg+/-, Ct, and Cg+/-, and they differ by the arrangement around the C-O and Calpha-C bonds. The ground-state Tt conformer is the only form present at 8 K after deposition of an argon matrix containing propionic acid. For the CH3CH2COOH and CH3CH2COOD isotopologues, narrow-band excitation of the first hydroxyl stretching overtone of the conformational ground state promotes the Calpha-C and C-O internal rotations producing the Tg+/- and Ct conformers, respectively. A subsequent vib…

Quantitative Biology::BiomoleculesArgon010304 chemical physicsOvertonechemistry.chemical_element010402 general chemistryPhotochemistry01 natural sciences0104 chemical sciences3. Good healthCrystallographychemistryAb initio quantum chemistry methods0103 physical sciencesMoleculeIsotopologuePhysics::Chemical PhysicsPhysical and Theoretical ChemistryGround stateConformational isomerismIsomerizationThe Journal of Physical Chemistry A
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Local dynamics of DNA probed with optical absorption spectroscopy of bound ethidium bromide

1997

We have studied the local dynamics of calf thymus double-helical DNA by means of an "optical labeling" technique. The study has been performed by measuring the visible absorption band of the cationic dye ethidium bromide, both free in solution and bound to DNA, in the temperature interval 360-30 K and in two different solvent conditions. The temperature dependence of the absorption line shape has been analyzed within the framework of the vibronic coupling theory, to extract information on the dynamic properties of the system; comparison of the thermal behavior of the absorption band of free and DNA-bound ethidium bromide gave information on the local dynamics of the double helix in the prox…

Quantitative Biology::BiomoleculesBinding SitesAbsorption spectroscopyChemistryAnharmonicityAnalytical chemistryBiophysicsDNASoft modesChromophoreNucleic Acid DenaturationSpectral lineSolutionsKineticsVibronic couplingSpectrophotometryAbsorption bandChemical physicsEthidiumHelixNucleic Acid ConformationThermodynamicsPhysics::Chemical PhysicsResearch ArticleBiophysical Journal
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Homology modeling of an RNP domain from a human RNA-binding protein: Homology-constrained energy optimization provides a criterion for distinguishing…

1998

We have recently described an automated approach for homology modeling using restrained molecular dynamics and simulated annealing procedures (Li et al, Protein Sci., 6:956-970,1997). We have employed this approach for constructing a homology model of the putative RNA-binding domain of the human RNA-binding protein with multiple splice sites (RBP-MS). The regions of RBP-MS which are homologous to the template protein snRNP U1A were constrained by "homology distance constraints," while the conformation of the non-homologous regions were defined only by a potential energy function. A full energy function without explicit solvent was employed to ensure that the calculated structures have good …

Quantitative Biology::BiomoleculesBiologyEnergy minimizationBiochemistryHomology (biology)CrystallographyMolecular dynamicsProtein structureStructural BiologySimulated annealingHomology modelingLoop modelingThreading (protein sequence)Biological systemMolecular BiologyProteins: Structure, Function, and Genetics
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Interacting induced dipoles polarization model for molecular polarizabilities: application to benzothiazole (A)-benzobisthiazole (B) oligomers AB13A

1998

Abstract We have outlined a method for the calculation of atomic net charges and molecular dipole-dipole,  α , dipole-quadrupole,  A , and quadrupole-quadrupole,  C , polarizabilities which we have successfully applied to benzothiazole (A)-benzobisthiazole (B) oligomers in the series AB1A to AB13A, and the results have been extrapolated to give predictions for polybenzobisthiazole. The calculation of  α ,  A and  C has been carried out by the interacting induced dipoles polarization model that calculates tensor effective anisotropic point polarizabilities (method of Applequist). The mean effective atomic αeffpolarizabilities for the monomeric unit are of the same order of magnitud…

Quantitative Biology::BiomoleculesBond dipole momentChemistryTransition dipole momentCondensed Matter PhysicsBiochemistryMolecular physicsOligomerAccessible surface areaDipolechemistry.chemical_compoundMonomerComputational chemistryQuadrupoleMoleculePhysics::Atomic PhysicsPhysical and Theoretical ChemistryJournal of Molecular Structure: THEOCHEM
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