arXiv subjects

Jürgen Köfinger

Publications and source records attributed to Jürgen Köfinger.

7 recordsLinked to original sources

arXiv2018

CADISHI: Fast parallel calculation of particle-pair distance histograms on CPUs and GPUs

We report on the design, implementation, optimization, and performance of the CADISHI software package, which calculates histograms of pair-distances of ensembles of particles on CPUs and GPUs. These histograms represent 2-point spatial correlation functions and are routinely calculated from simulations of soft and condensed matter, where they are referred to as radial distribution functions, and in the analysis of the spatial distributions of galaxies and galaxy clusters. Although conceptually simple, the calculation of radial distribution functions via distance binning requires the evaluation of $\mathcal{O}(N^2)$ particle-pair distances where $N$ is the number of particles under consideration. CADISHI provides fast parallel implementations of the distance histogram algorithm for the CPU and the GPU, written in templated C++ and CUDA. Orthorhombic and general triclinic periodic boxes are supported, in addition to the non-periodic case. The CPU kernels feature cache-blocking, vectorization and thread-parallelization to obtain high performance. The GPU kernels are tuned to exploit the memory and processor features of current GPUs, demonstrating histogramming rates of up to a factor 40 higher than on a high-end multi-core CPU. To enable high-throughput analyses of molecular dynamics trajectories, the compute kernels are driven by the Python-based CADISHI engine. It implements a producer-consumer data processing pattern and thereby enables the complete utilization of all the CPU and GPU resources available on a specific computer, independent of special libraries such as MPI, covering commodity systems up to high-end HPC nodes. Data input and output are performed efficiently via HDF5. (...) The CADISHI software is freely available under the MIT license.

physics.comp-ph↗

arXiv2018

Hydrodynamics of Diffusion in Lipid Membrane Simulations

By performing molecular dynamics simulations with up to 132 million coarse-grained particles in half-micron sized boxes, we show that hydrodynamics quantitatively explains the finite-size effects on diffusion of lipids, proteins, and carbon nanotubes in membranes. The resulting Oseen correction allows us to extract infinite-system diffusion coefficients and membrane surface viscosities from membrane simulations despite the logarithmic divergence of apparent diffusivities with increasing box width. The hydrodynamic theory of diffusion applies also to membranes with asymmetric leaflets and embedded proteins, and to a complex plasma-membrane mimetic.

cond-mat.soft↗

arXiv2018

Phase Transition and Interpore Correlations of Water in Nanopore Membranes

Using computer simulations, we study a membrane of parallel narrow pores filled with one-dimensional wires of hydrogen-bonded water molecules. We show that such a membrane is equivalent to a system of effective charges located at opposite sides of the membrane offering a computationally efficient way to model correlation effects in water-filled nanopore membranes. Based on our simulations we predict that membranes with square pore lattices undergo a continuous order-disorder transition to an antiferroelectric low-temperature phase in which water wires in adjacent pores are oriented in opposite directions. Strong antiferroelectric correlations exist also in the disordered phase far above the critical temperature or in membranes with geometric frustration, leading to a dielectric constant that is reduced considerably with respect to the case of uncoupled water wires. These correlations are also expected to hinder proton translocation through the membrane.

physics.comp-ph↗

arXiv2015

Bayesian ensemble refinement by replica simulations and reweighting

We describe different Bayesian ensemble refinement methods, examine their interrelation, and discuss their practical application. With ensemble refinement, the properties of dynamic and partially disordered (bio)molecular structures can be characterized by integrating a wide range of experimental data, including measurements of ensemble-averaged observables. We start from a Bayesian formulation in which the posterior is a functional that ranks different configuration space distributions. By maximizing this posterior, we derive an optimal Bayesian ensemble distribution. For discrete configurations, this optimal distribution is identical to that obtained by the maximum entropy "ensemble refinement of SAXS" (EROS) formulation. Bayesian replica ensemble refinement enhances the sampling of relevant configurations by imposing restraints on averages of observables in coupled replica molecular dynamics simulations. We show that the strength of the restraint should scale linearly with the number of replicas to ensure convergence to the optimal Bayesian result in the limit of infinitely many replicas. In the "Bayesian inference of ensembles" (BioEn) method, we combine the replica and EROS approaches to accelerate the convergence. An adaptive algorithm can be used to sample directly from the optimal ensemble, without replicas. We discuss the incorporation of single-molecule measurements and dynamic observables such as relaxation parameters. The theoretical analysis of different Bayesian ensemble refinement approaches provides a basis for practical applications and a starting point for further investigations.

physics.data-an↗

arXiv2009

The statistics of electric field fluctuations in liquid water

Electric field fluctuations play a major role in dissociation reactions in liquid water and determine its vibrational spectroscopic response. Here, we study the statistics of electric fields in liquid water using molecular dynamics computer simulations with a particular focus on the strong but rare fields that drive dissociation. Our simulations indicate that the important contributions to the electric field acting on OH bonds stem from water molecules less than 7 Å away. Long-ranged contributions play a minor role.

cond-mat.stat-mech↗

arXiv2009

A one-dimensional dipole lattice model for water in narrow nanopores

We present a recently developed one-dimensional dipole lattice model that accurately captures the key properties of water in narrow nanopores. For this model, we derive three equivalent representations of the Hamiltonian that together yield a transparent physical picture of the energetics of the water chain and permit efficient computer simulations. In the charge representation, the Hamiltonian consists of nearest-neighbor interactions and Coulomb-like interactions of effective charges at the ends of dipole ordered segments. Approximations based on the charge picture shed light on the influence of the Coulomb-like interactions on the structure of nanopore water. We use Monte Carlo simulations to study the system behavior of the full Hamiltonian and its approximations as a function of chemical potential and system size and investigate the bimodal character of the density distribution occurring at small system sizes.

physics.chem-ph↗

arXiv2007

Biasing the center of charge in molecular dynamics simulations with empirical valence bond models: free energetics of an excess proton in a water droplet

Multistate empirical valence bond (EVB) models provide an accurate description of the energetics of proton transfer and solvation in complex molecular systems and can be efficiently used in molecular dynamics computer simulations. Within such models, the location of the moving protonic charge can be specified by the so called center of charge, defined as a weighted average over the diabatic states of the EVB model. In this paper, we use first order perturbation theory to calculate the molecular forces that arise if a bias potential is applied to the center of charge. Such bias potentials are often necessary when molecular dynamics simulations are used to determine free energies related to proton transfer and not all relevant proton positions are sampled with sufficient frequency during the available computing time. The force expressions we derive are easy to evaluate and do not create any significant computational cost compared with unbiased EVB-simulations. As an illustration of the method, we study proton transfer in a small liquid water droplet consisting of 128 water molecules plus an excess proton. Contrary to predictions of continuum electrostatics but in agreement with previous computer simulations of similar systems, we observe that the excess proton is predominantly located at the surface of the droplet. Using the formalism developed in this paper, we calculate the reversible work required to carry the protonic charge from the droplet surface to its core finding a value of roughly 4 $k_{\rm B}T$.

cond-mat.soft↗