Search results for "Random coil"

showing 10 items of 22 documents

Aggregation Kinetics of Bovine Serum Albumin Studied by FTIR Spectroscopy and Light Scattering

2003

To investigate which type of structural and conformational changes is involved in the aggregation processes of bovine serum albumin (BSA), we have performed thermal aggregation kinetics in D(2)O solutions of this protein. The tertiary conformational changes are followed by Amide II band, the secondary structural changes and the formation of beta-aggregates by the Amide I' band and, finally, the hydrodynamic radius of aggregates by dynamic light scattering. The results show, as a function of pD, that: tertiary conformational changes are more rapid as pD increases; the aggregation proceeds through formation of ordered aggregates (oligomers) at pD far from the isoelectric point of the protein;…

Protein ConformationKineticsBiophysicsProtein aggregationBiochemistryProtein Structure SecondaryProtein structureDynamic light scatteringSpectroscopy Fourier Transform InfraredAnimalsScattering RadiationStatic light scatteringDeuterium OxideBovine serum albuminInfrared spectroscopyStatic light scatteringbiologyChemistryOrganic ChemistryTemperatureSerum Albumin BovineConformational changeRandom coilProtein tertiary structureKineticsCrystallographyBovine serum albuminbiology.proteinDynamic light scatteringCattleProtein aggregation
researchProduct

Simulation of Phase Transitions of Single Polymer Chains: Recent Advances

2006

The behaviour of a flexible polymer chain in solvents of variable quality in dilute solution is discussed both in the bulk and in the presence of an adsorbing wall. Monte Carlo simulations of coarse-grained bead-spring models and of the bond fluctuation model are presented and interpreted in terms of phenomenological theories and scaling concepts. Particular attention is paid to the behaviour of the polymer chain when the temperature of the polymer solution gets lower than the Theta temperature. It is argued that the adsorption transition line at the Theta temperature splits into lines of wetting and drying transitions of polymer globules attached to the wall. In addition, it is shown that …

Quantitative Biology::BiomoleculesPhase transitionPolymers and PlasticsChemistryCrystallization of polymersOrganic ChemistryThermodynamicsCoil-globule transitionCondensed Matter PhysicsRandom coilCondensed Matter::Soft Condensed MatterMean field theoryThermodynamic limitMaterials ChemistryVirial expansionScalingMacromolecular Symposia
researchProduct

The phase diagram of a single polymer chain: New insights from a new simulation method

2006

We present simulation results for the phase behavior of a single chain for a flexible lattice polymer model using the Wang-Landau sampling idea. Applying this new algorithm to the problem of the homopolymer collapse allows us to investigate not only the high temperature coil–globule transition but also an ensuing crystallization at lower temperature. Performing a finite size scaling analysis on the two transitions, we show that they coincide for our model in the thermodynamic limit corresponding to a direct collapse of the random coil into the crystal without intermediate coil–globule transition. As a consequence, also the many chain phase diagram of this model can be predicted to consist o…

Quantitative Biology::BiomoleculesPolymers and PlasticsChemistryMonte Carlo methodThermodynamicsCondensed Matter PhysicsRandom coillaw.inventionlawLattice (order)Thermodynamic limitMaterials ChemistryDensity of statesStatistical physicsPhysical and Theoretical ChemistryCrystallizationScalingPhase diagramJournal of Polymer Science Part B: Polymer Physics
researchProduct

Critical micellisation density: a SAS structural study of the unimer–aggregate transition of block-copolymers in supercritical CO2

2000

In this paper we report a SANS investigation of micelle formation by fluorocarbon-hydrocarbon block copolymers in supercritical CO2 (scCO2) at 313K. A sharp unimer-micelle transition is obtained due to the tuning of the solvating ability of scCO2 by profiling pressure. At high pressure the copolymer is in a monomeric state with a random coil structure. By lowering the pressure aggregates are formed with the hydrocarbon segments forming the core and the fluorocarbon segments forming the corona of spherical aggregates. This aggregateunimer transition is driven by the gradual penetration of CO2 molecules toward the core of the aggregate and is critically related to the density of the solvent, …

Solventchemistry.chemical_compoundMonomerchemistryChemical engineeringPolymer chemistryCopolymerMoleculeFluorocarbonMicelleGeneral Biochemistry Genetics and Molecular BiologySupercritical fluidRandom coilJournal of Applied Crystallography
researchProduct

Conformational analysis of α,β-poly(N-hydroxyethyl)-dl-aspartamide (PHEA) and α,β-polyasparthydrazide (PAHy) polymers in aqueous solution

1998

Abstract α,β-Poly(N-hydroxyethyl)- dl -aspartamide (PHEA) and α,β-polyasparthydrazide (PAHy) are synthetic polymers previously studied for biomedical applications. We report here the results of a small-angle X-ray scattering analysis carried out on these two macromolecules in aqueous solution. The data obtained indicate that the two polymers assume remarkably different conformations in aqueous solution, although the backbone is supposed to be the same for the two chains. PHEA can be represented by a random coil conformation, whereas PAHy can be described in terms of an elliptical cylinder characterized by an almost planar structural arrangement with the backbone refolded on itself in a fash…

chemistry.chemical_classificationAqueous solutionElliptical cylinderPolymers and PlasticsChemistryHydrogen bondSmall-angle X-ray scatteringGlobular proteinOrganic ChemistryPolymerRandom coilPolymer chemistryMaterials ChemistryMacromoleculePolymer
researchProduct

Solution Properties and Potential Biological Applications of Zwitterionic Poly(ε-N-methacryloyl-l-lysine)

2013

Poly(e-N-methacryloyl-l-lysine) (PMALys) was synthesized by free radical polymerization yielding a zwitterionic polymer with Mw = 721 000 g mol–1. The polymer dissolves in pure water as well as in aqueous salt solution up to 5 M NaClO4 and over wide range of pH values (1.3 ≤ pH ≤ 12.7) as single chains without any sign for aggregate formation. The zwitterionic polymer shows an expanded random coil structure at and close to isoelectric conditions and further expands upon addition of acid and base, respectively. The polymer fulfills four major prerequisites for a promising nano carrier in potential biomedical applications: (1) It is biocompatible, indicated by a low cytotoxicity. (2) It does …

chemistry.chemical_classificationAqueous solutionPolymers and PlasticsChemistryOrganic ChemistryLysineRadical polymerizationPolymerRandom coilInorganic ChemistryIsoelectric pointPolymer chemistryMaterials ChemistryAcid–base reactionCytotoxicityMacromolecules
researchProduct

Revisiting Secondary Structures in NCA Polymerization: Influences on the Analysis of Protected Polylysines

2014

Two series (degree of polymerization: 20–200) of polylysines with Z and TFA protecting groups were synthesized, and their behavior in a range of analytical methods was investigated. Gel permeation chromatography of the smaller polypeptides reveals a bimodal distribution, which is lost in larger polymers. With the help of GPC, NMR, circular dichroism (CD), and MALDI-TOF, it was demonstrated that the bimodal distribution is not due to terminated chains or other side reactions. Our results indicate that the bimodality is caused by a change in secondary structure of the growing peptide chain that occurs around a degree of polymerization of about 15. This change in secondary structure interferes…

chemistry.chemical_classificationCircular dichroismPolymers and PlasticsOrganic ChemistryPeptidePolymerDegree of polymerizationRandom coilInorganic ChemistryGel permeation chromatographychemistryPolymerizationPolymer chemistryMaterials ChemistryProtein secondary structureMacromolecules
researchProduct

Modelling small angle neutron scattering data from polymers in supercritical fluids

2000

In this paper we report a SANS investigation of micelle formation by fluorocarbon-hydrocarbon block copolymers in supercritical CO2(scCO2) at 313K. A sharp unimer-micelle transition is obtained due to the tuning of the solvating ability of scCO2 by profiling pressure. At high pressure the copolymer is in a monomeric state with a random coil structure. By lowering the pressure aggregates are formed with the hydrocarbon segments forming the core and the fluorocarbon segments forming the corona of spherical aggregates. This aggregate-unimer transition is driven by the gradual penetration of CO2 molecules toward the core of the aggregate and is critically related to the density of the solvent, …

chemistry.chemical_classificationCrystallographyMaterials sciencechemistryChemical physicsCopolymerSolvationPolymerFluorocarbonSmall-angle neutron scatteringMicelleSupercritical fluidRandom coilAIP Conference Proceedings
researchProduct

Molecular motion, thermal expansion, and phase transitions in paraffins: A model for polymers

2007

Owing to their simple chemical structure paraffins are generally regarded as representing a system which is especially suitable for a model study of the thermal behavior of oligomeric and polymeric solids. Extensive investigations on the properties of n-tritriacontane (C33H68) provide an example. For this system an identification of several types of motional mechanisms become possible. Their presence leads to peculiarities in the thermal expansion and to the occurrence of solid-solid phase transitions. Paraffins and polyethylene exhibit a marked anisotropy in the lateral thermal expansion. An analysis of the molecular background can be based on a modified Gruneisen theory which connects exp…

chemistry.chemical_classificationPhase transitionChemistryStereochemistryAnharmonicityGeneral EngineeringThermodynamicsPolymerThermal expansionRandom coilsymbols.namesakeThermalsymbolsAnisotropyRaman spectroscopyJournal of Polymer Science: Polymer Symposia
researchProduct

On the first-order collapse transition of a three-dimensional, flexible homopolymer chain model

2005

We present simulation results for the phase behavior of flexible lattice polymer chains using the Wang-Landau sampling idea. These chains display a two-stage collapse through a coil-globule transition followed by a crystallization at lower temperatures. Performing a finite-size scaling analysis on the two transitions, we show that they coincide in the thermodynamic limit corresponding to a direct collapse of the random coil into the crystal without intermediate coil-globule transition.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesChain modelMaterials scienceGeneral Physics and AstronomyThermodynamicsPolymerFirst orderRandom coillaw.inventionchemistrylawLattice (order)Thermodynamic limitCrystallizationScalingEurophysics Letters (EPL)
researchProduct