Search results for "Biomolecules"

showing 10 items of 549 documents

Atomistic Molecular Dynamics Simulations of the Static and Dynamic Properties of a Polyethylene Melt

1999

I will discuss in this work the atomistic modelling of polymer melts using Molecular Dynamics (MD) simulations. After a general introduction into the problems one faces in the computer simulation of polymers in general and the atomistic simulations in particular, I will present some recent work on the atomistic modelling of an — C 100 H 202 melt,i.e. short chain polyethylene (PE). The aim of this work is to establish a quantitatively validated atomistic model which then can be used in two directions. One direction is the generation of input for the calibration of parameters in coarse-grained models, which in turn can be used to simulate the polymer under investigation over a much broader te…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesWork (thermodynamics)Molecular dynamicsMaterials sciencechemistryDynamic structure factorRelaxation (NMR)PolymerStatistical physicsStructure factorSpectral lineNeutron spin echo
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Entropy theory and glass transition: A test by Monte Carlo simulation

1997

This article reviews the results of a test of the Gibbs-DiMarzio theory by Monte Carlo Simulation. The simulation employed the bond-fluctuation model on a simple cubic lattice. This model incorporates two kinds of interactions: the excluded volume interaction among all monomers of the melt and an internal energy of the chains, which favors large bonds and makes the chains stiffen with decreasing temperature. The stiffening of the chains leads to an increase of their volume requirements, which competes with the packing constraints at low temperatures. This competition strongly slows down the structural relaxation of the melt and induces the glassy behavior. The model therefore takes into acc…

chemistry.chemical_classificationQuantitative Biology::Biomoleculesbond-fluctuation modelMaterials scienceInternal energyMonte Carlo methodGibbs-DiMarzio theoryGeneral EngineeringThermodynamicsSimple cubic latticePolymerArticleStiffeningCondensed Matter::Soft Condensed Matterentropy measurementchemistryExcluded volumeAdam-Gibbs theoryEntropy (information theory)chemical potentialglass transitionStatistical physicsdiffusion coefficientGlass transitionMonte Carlo simulation
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Allylammonium hydrogen oxalate hemihydrate

2014

In the title hydrated molecular salt, C3H8N+·C2HO4−·0.5H2O, the water O atom lies on a crystallographic twofold axis. The C=C—C—N torsion angle in the cation is 2.8 (3)° and the dihedral angle between the CO2and CO2H planes in the anion is 1.0 (4)°. In the crystal, the hydrogen oxalate ions are linked by O—H...O hydrogen bonds, generating [010] chains. The allylammonium cations bond to the chains through N—H...O and N—H...(O,O) hydrogen bonds. The water molecule accepts two N—H...O hydrogen bonds and makes two O—H...O hydrogen bonds. Together, the hydrogen bonds generate (100) sheets.

chemistry.chemical_classificationQuantitative Biology::Biomoleculescrystal structureCrystallographyHydrogenHydrogen bondchemistry.chemical_elementSalt (chemistry)General ChemistryCrystal structureDihedral angleCondensed Matter PhysicsOrganic PapersOxalateIonCrystalCrystallographychemistry.chemical_compoundchemistryQD901-999General Materials SciencePhysics::Atomic PhysicsPhysics::Chemical PhysicsActa Crystallographica Section E-Structure Reports Online
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Temperature effects on counterion binding to spherical polyelectrolytes: the charge-discharge transition of lignosulfonate

1995

Abstract The effect of temperature on the effective charge numbers and diffusion coefficients of polyelectrolytes has not nobee dealth with in many studies. The present study concerns the temperature behavior of lignosulfonate. Lignosulfonate is a polydisperse polyelectrolyte whose molecules are compact spheres in aqueous solutions. One of its most remarkable properties is that is loses its charge in 0.1 M NaCl aqueous solution at about 40°C. In order to explain this charge-discharge transition, a theory for ion binding to spherical polyelectrolytes based on the relative population of two hydration states of the charged groups is presented. The water molecules adjacent to the charged groups…

chemistry.chemical_classificationQuantitative Biology::Biomoleculeseducation.field_of_studyGlobular proteinInorganic chemistryPopulationBiophysicsCharge numberElectrolyteIon-associationEffective nuclear chargePolyelectrolyteCondensed Matter::Soft Condensed MatterIon bindingchemistryChemical physicsElectrochemistryPhysical and Theoretical ChemistryeducationBioelectrochemistry and Bioenergetics
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Conformational studies of bottle-brush polymers absorbed on a flat solid surface.

2010

The adsorption of a bottle-brush polymer end-grafted with one chain end of its backbone to a flat substrate surface is studied by Monte Carlo simulation of a coarse-grained model, that previously has been characterized in the bulk, assuming a dilute solution under good solvent conditions. Applying the bond fluctuation model on the simple cubic lattice, we vary the backbone chain length $N_b$ from $N_b=67$ to $N_b = 259$ effective monomeric units, the side chain length $N$ from N=6 to N=48, and the grafting density $\sigma=1$, i.e., parameters that correspond well to the experimentally accessible range. When the adsorption energy strength $\epsilon$ is varied, we find that the adsorption tra…

chemistry.chemical_classificationRange (particle radiation)Quantitative Biology::BiomoleculesMaterials scienceMonte Carlo methodGeneral Physics and AstronomyBackbone chainThermodynamicsFOS: Physical sciencesPolymerCondensed Matter - Soft Condensed MatterGyrationCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundMonomerAdsorptionchemistrySide chainSoft Condensed Matter (cond-mat.soft)Physical and Theoretical ChemistryThe Journal of chemical physics
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Monte Carlo methods for polymer chains in two - dimensional geometries (polymers at surfaces and interfaces)

1993

Coarse-grained models of polymers at interfaces can be defined such that their treatment by Monte Carlo simulation is most convenient and efficient for the problem at hand. This simulation strategy is briefly illustrated with three examples: (1) The orientational ordering of rigid rod-like polymers grafted to a surface, where “table methods” can be used, applying a fine discretization of the angles describing rod orientation. (2) Surface enrichment of one species in a polymer blend is treated by a semi-grand-canonical technique. (3) The number of configurations and structure of a star polymer attached with its center to a wall is studied by a “growth technique” generalizing simple sampling …

chemistry.chemical_classificationSurface (mathematics)Quantitative Biology::BiomoleculesMaterials sciencePolymers and PlasticsDiscretizationOrganic ChemistryMonte Carlo methodPolymerCondensed Matter PhysicsCondensed Matter::Soft Condensed MatterchemistryComputational chemistrySimple (abstract algebra)Orientation (geometry)Materials ChemistryPolymer blendStatistical physicsMakromolekulare Chemie. Macromolecular Symposia
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Chain linear dimensions in the surface-enriched layer of polymer mixtures

1992

We calculate the mean-square end-to-end distances and mean-square gyration radii using the bond fluctuation model for a binary polymer blend in the presence of a wall by Monte Carlo simulation. In the bulk, the size of the minority, low-concentration polymer species is compressed compared to the majority one. In the vicinity of the wall, where the minority polymer concentration is enriched due to attraction from the wall, the dimensions of the two types of polymers are approximately equal and are essentially the same as in an athermal polymer melt. Thus, the geometric constraint is more important to the structure of the polymers than the polymer-polymer and polymer-wall interactions.

chemistry.chemical_classificationSurface (mathematics)Quantitative Biology::BiomoleculesMonte Carlo methodMineralogyPolymer architecturePolymerGyrationCondensed Matter::Soft Condensed MatterchemistryChain (algebraic topology)Chemical physicsPolymer blendLayer (electronics)Die Makromolekulare Chemie, Theory and Simulations
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Dynamics of macromolecules grafted in spherical brushes under good solvent conditions

2013

Spherical polymer brushes have a structure intermediate between star polymers and polymer brushes on flat substrates, and are important building blocks of polymer nanoparticles. Molecular dynamics simulations are presented for isolated spherical polymer brushes under good solvent conditions, varying the grafting density as well as the chain length, using a coarse-grained bead-spring model of flexible chains. We complement previous work on the static properties of the same model by analyzing the chain dynamics, studying the motions of monomers in relation to their position along the grafted chains, and extract suitable relaxation times. A qualitative discussion in terms of the Rouse model is…

chemistry.chemical_classificationWork (thermodynamics)Quantitative Biology::BiomoleculesPolymers and PlasticsPolymer scienceOrganic ChemistryRelaxation (NMR)NanoparticlePolymerInorganic ChemistryCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundMolecular dynamicsPlanarMonomerchemistryMaterials ChemistryMacromoleculeMacromolecules
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Sorting of Enhanced Reference Raman Spectra of a Single Amino Acid Molecule

2014

In this contribution, we report the identification of the principal reference Raman spectra of a single cystein molecule. To that purpose, we design an active Surface Enhanced Raman Spectroscopy (SERS) template based on surfactant-less Chebyshev nanoparticles operating in a microfluidic platform. A principal component analysis is obtained from fluctuating spectra to sort the reference spectra of cystein. The assignment of Raman bands brings new insight into the conformation of an amino acid adsorbed onto gold nanoparticle.

chemistry.chemical_classification[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics]Quantitative Biology::BiomoleculesSortingNanoparticleActive surfaceQuantitative Biology::GenomicsSpectral lineSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAmino acidCrystallographysymbols.namesakeGeneral EnergyAdsorptionchemistrysymbolsMoleculePhysical and Theoretical ChemistryRaman spectroscopyComputingMilieux_MISCELLANEOUSThe Journal of Physical Chemistry C
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Simulated eutrophication and browning alters zooplankton nutritional quality and determines juvenile fish growth and survival

2018

Source at https://doi.org/10.1002/ece3.3832. The first few months of life is the most vulnerable period for fish and their optimal hatching time with zooplankton prey is favored by natural selection. Traditionally, however, prey abundance (i.e., zooplankton density) has been considered important, whereas prey nutritional composition has been largely neglected in natural settings. High‐quality zooplankton, rich in both essential amino acids (EAAs) and fatty acids (FAs), are required as starting prey to initiate development and fast juvenile growth. Prey quality is dependent on environmental conditions, and, for example, eutrophication and browning are two major factors defining primary produ…

compound‐specific stable isotopesDAPHNIArasvahapotcompound-specific stable isotopesaminohapotbiomolekyylitfatty acidsFOOD WEBSORGANIC-CARBONLAKE ECOSYSTEMSPRIMARY PRODUCERSessential biomoleculesVDP::Landbruks- og Fiskerifag: 900::Fiskerifag: 920Original ResearchPOLYUNSATURATED FATTY-ACIDSisotoopitVDP::Agriculture and fishery disciplines: 900::Fisheries science: 920amino acidsfood webfunginutritional qualityDOCOSAHEXAENOIC ACID1181 Ecology evolutionary biologyravintoarvoFRESH-WATER MICROALGAELIPID-COMPOSITIONravintoverkotSOMATIC GROWTH
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