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Molecular Dynamics Simulation of Aqueous Urea Solution: Is Urea a Structure Breaker?

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TLDR
It is suggested that urea is able to substitute for water in the hydrogen-bonded network nicely without breaking the tetrahedral, hydrogen- bonded structure of water.
Abstract
An aqueous solution of urea is a very important mixture of biological relevance because of the definitive role of urea as protein denaturant at high concentrations. There has been an extended debate over the years on urea’s influence on the structure of water. On the basis of a variety of analysis methods employed, urea has been described as a structure-breaker, a structure-maker, or as neutral toward water structure. Using molecular dynamics simulation and a nearest neighbor approach of analyzing water structure, we present here a detailed analysis of the effect of urea on water structure. By carefully choosing the nearest neighbors, allowing urea also to be a neighbor of a reference water molecule, we have conclusively shown that urea does not break the local tetrahedral structure of water even at high concentrations. A slight change in the distribution of tetrahedral order parameters as a function of urea concentration has been shown to be a result of change in the proportions of n-hydrogen-bonded wate...

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Citations
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Journal ArticleDOI

Characterization of the Local Structure in Liquid Water by Various Order Parameters.

TL;DR: This work considers a series of popular order parameters and analyzes molecular dynamics simulations of water, in the bulk and in the hydration shell of a hydrophobic solute, at 298 and 260 K to confirm the absence of any iceberg-type structure.
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Density relaxation and particle motion characteristics in a non-ionic deep eutectic solvent (acetamide + urea): Time-resolved fluorescence measurements and all-atom molecular dynamics simulations

TL;DR: Temperature dependent relaxation dynamics, particle motion characteristics, and heterogeneity aspects of deep eutectic solvents made of acetamide and urea have been investigated by employing time-resolved fluorescence measurements and all-atom molecular dynamics simulations and suggest a fundamental difference in interaction and dynamics between ionic and non-ionic deep eutsenic solvent systems.
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Influence of TMAO and urea on the structure of water studied by inelastic X-ray scattering

TL;DR: The experiment shows that the hydrogen-bonding structure of water remains rather intact in the presence of the aforementioned osmolytes if both of them are present, and this compensation effect seen in the spectra vanishes only at the highest studied ternary concentration.
Journal ArticleDOI

TMAO and urea in the hydration shell of the protein SNase

TL;DR: All-atom MD simulations of the protein SNase in aqueous solution and in the presence of two major osmolytes, trimethylamine-N-oxide (TMAO) and urea, as cosolvents found that the cosolvent molecules have a small but significant effect on the apparent volume and its contributions, i.e. the intrinsic, molecular and thermal volumes.
Journal ArticleDOI

Role of Urea-Aromatic Stacking Interactions in Stabilizing the Aromatic Residues of the Protein in Urea-Induced Denatured State.

TL;DR: It is shown here that the remarkable ability of urea to form stacking and NH-π interactions with aromatic groups of proteins are crucial in urea-assisted RNA unfolding and that such interactions are possible for all the aromatic amino acid side-chains.
References
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Journal ArticleDOI

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TL;DR: In this paper, a method is described to realize coupling to an external bath with constant temperature or pressure with adjustable time constants for the coupling, which can be easily extendable to other variables and to gradients, and can be applied also to polyatomic molecules involving internal constraints.
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Particle mesh Ewald: An N⋅log(N) method for Ewald sums in large systems

TL;DR: An N⋅log(N) method for evaluating electrostatic energies and forces of large periodic systems is presented based on interpolation of the reciprocal space Ewald sums and evaluation of the resulting convolutions using fast Fourier transforms.
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A smooth particle mesh Ewald method

TL;DR: It is demonstrated that arbitrary accuracy can be achieved, independent of system size N, at a cost that scales as N log(N), which is comparable to that of a simple truncation method of 10 A or less.
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GROMACS 4: Algorithms for highly efficient, load-balanced, and scalable molecular simulation

TL;DR: A new implementation of the molecular simulation toolkit GROMACS is presented which now both achieves extremely high performance on single processors from algorithmic optimizations and hand-coded routines and simultaneously scales very well on parallel machines.
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Polymorphic transitions in single crystals: A new molecular dynamics method

TL;DR: In this paper, a new Lagrangian formulation is introduced to make molecular dynamics (MD) calculations on systems under the most general externally applied, conditions of stress, which is well suited to the study of structural transformations in solids under external stress and at finite temperature.
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