1,479 research outputs found
Particles and Fields in Superfluids: Insights from the Two-dimensional Gross-Pitaevskii Equation
We study the dynamics of active particles in two-dimensional superfluids at temperature , for a variety of initial configurations, by carrying out extensive direct-numerical-simulations of the two-dimensional, Galerkin-truncated Gross-Pitaevskii equation. Our study elucidates the interplay of particles and fields, in both simple and turbulent flows. We show that particle collisions can be inelastic, if the repulsive interactions between particles is weak, and elastic otherwise. We show that assemblies of many particles and vortices yield turbulent spatiotemporal evolutions
Semiflexible equilibrium polymers: A self-assembling molecular model
We propose a continuum molecular model for self-assembling, semiflexible,
equilibrium polymers and study its statistical mechanics by Monte Carlo (MC)
simulations. If the temperature (T) is high, we find a disordered phase
in which the mean length of polymers is
small. A first-order transition separates it from a low-T
phase in which is larger and the
semiflexible polymers are aligned enough to yield nematic
ordering. Disordered, glassy states can be obtained at low T; we
study these by an MC analogue of scanning calorimetry (Menon G. I., Pandit R. and Barma M.,
Europhys. Lett., 24 (1993) 253;
Menon G. I. and Pandit R., Phys. Rev. Lett., 75 (1995) 4638;
Phys. Rev. E, 59 (1999) 787).
We also use an MC method to study shear alignment of polymers
(Berret J. F., Roux D. C. and Porte G.,
J. Phys. II, 4 (1994) 1261;
Berret J. F., Roux D. C., Porte G. and Lindner P.,
Europhys. Lett., 25 (1994)521)
in our model)
Mutual-Friction Coefficients in Two-Dimensional Superfluids: From the Gross-Pitaevskii equation to the Hall-Vinen-Bekharevich-Khalatnikov Two-fluid Model
We start from the two-dimensional Gross-Pitaevskii equation (GPE) and develop algorithms for the ab-initio determination of the temperature (T) dependence of the mutual-friction coefficients, α and α, and the normal-fluid density Pn, which appear as parameters in the Hall-Vinen-Bekharevich-Khalatnikov (HVBK) two-fluid model for a superfluid. In the second part of our study, we elucidate the statistical properties of two-dimensional, homogeneous, isotropic superfluid turbulence in the simplified HVBK model, with values for the mutual-friction coefficients that are comparable to those we obtain from the first part of our study
Spinodal decomposition in the inverse cascade of two-dimensional, binary-fluid turbulence
We study spinodal decomposition in the inverse-cascade regime of two dimensional turbulence in symmetric, binary fluid mixtures. We show that turbulence leads to break up of domains whose size, in the inverse cascade regime, is proportional to the Hinze scale. Even more strikingly, we show that the inverse cascade of energy is blocked by the formation of domains
Multifractal Droplet Dynamics in Two-Dimensional, binary-fluid turbulence
We present the most extensive direct numerical simulations, attempted so far, of statistically steady, homogeneous, isotropic turbulence in two-dimensional, binary-fluid mixtures with air-drag-induced friction. We model this mixture by using the Cahn-Hilliard-Navier-Stokes equations and choose parameters, e.g., the surface tension, such that we have a droplet of the minority phase moving inside a turbulent background of the majority phase. Our study reveals that a single droplet, whose mean radius lies in the inertial range of scales, (a) enhances the the forward-cascade part of the energy spectrum of two-dimensional turbulence and (b) stretches the tails of the PDF of the Okubo-Weiss parameter . We show that the dynamics of the droplet is affected significantly by the turbulence in the fluid. In particular, the PDFs of the components of the acceleration shows wide, non-Guassian tails. We characterize the time dependence of the deformation of the droplet and show that it exhibits multifractality
Real-space Manifestations of Bottlenecks in Turbulence Spectra
An energy-spectrum bottleneck, a bump in the turbulence spectrum between the inertial and dissipation ranges, is shown to occur in the non-turbulent, one-dimensional, hyperviscous Burgers equation and found to be the Fourier-space signature of oscillations in the real-space velocity, which are explained by boundary-layer-expansion techniques. Pseudospectral simulations are used to show that such oscillations occur in velocity correlation functions in one- and three-dimensional hyperviscous hydrodynamical equations that display genuine turbulence
Universal Statistical Properties of Inertial-particle Trajectories in Three-dimensional, Homogeneous, Isotropic, Fluid Turbulence
We obtain new universal statistical properties of heavy-particle trajectories in three-dimensional, statistically steady, homogeneous, and isotropic turbulent flows by direct numerical simulations. We show that the probability distribution functions (PDFs) P(Φ), of the angle Φ between the Eulerian velocity u and the particle velocity v, at a point and time, scales as P(Φ) ∼Φ−, with a new universal exponent ≃ 4
Surfactant protein D inhibits HIV-1 infection of target cells via interference with gp120-CD4 interaction and modulates pro-inflammatory cytokine production
© 2014 Pandit et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.Surfactant Protein SP-D, a member of the collectin family, is a pattern recognition protein, secreted by mucosal epithelial cells and has an important role in innate immunity against various pathogens. In this study, we confirm that native human SP-D and a recombinant fragment of human SP-D (rhSP-D) bind to gp120 of HIV-1 and significantly inhibit viral replication in vitro in a calcium and dose-dependent manner. We show, for the first time, that SP-D and rhSP-D act as potent inhibitors of HIV-1 entry in to target cells and block the interaction between CD4 and gp120 in a dose-dependent manner. The rhSP-D-mediated inhibition of viral replication was examined using three clinical isolates of HIV-1 and three target cells: Jurkat T cells, U937 monocytic cells and PBMCs. HIV-1 induced cytokine storm in the three target cells was significantly suppressed by rhSP-D. Phosphorylation of key kinases p38, Erk1/2 and AKT, which contribute to HIV-1 induced immune activation, was significantly reduced in vitro in the presence of rhSP-D. Notably, anti-HIV-1 activity of rhSP-D was retained in the presence of biological fluids such as cervico-vaginal lavage and seminal plasma. Our study illustrates the multi-faceted role of human SPD against HIV-1 and potential of rhSP-D for immunotherapy to inhibit viral entry and immune activation in acute HIV infection. © 2014 Pandit et al.The work (Project no. 2011-16850) was supported by Medical Innovation Fund of Indian Council of Medical Research, New Delhi, India (www.icmr.nic.in/)
sj-docx-1-jet-10.1177_15266028211064824 – Supplemental material for Clinical Utility of Intravascular Ultrasound (IVUS) in Carotid Artery Interventions: A Systematic Review and Meta-analysis
Supplemental material, sj-docx-1-jet-10.1177_15266028211064824 for Clinical Utility of Intravascular Ultrasound (IVUS) in Carotid Artery Interventions: A Systematic Review and Meta-analysis by B. Mishra, A. K. Pandit, S. Miyachi, T. Ohshima, R. Kawaguchi, V. Y. Vishnu, S. Misra, M. V. P. Srivastava, A. K. Srivastava, S. S. Kale and M. Phalak in Journal of Endovascular Therapy</p
Altered excitation-contraction coupling in human chronic atrial fibrillation
This review focuses on the (mal)adaptive processes in atrial excitation-contraction coupling occurring in patients with chronic atrial fibrillation. Cellular remodeling includes shortening of the atrial action potential duration and effective refractory period, depressed intracellular Ca<sup>2+</sup> transient, and reduced myocyte contractility. Here we summarize the current knowledge of the ionic bases underlying these changes. Understanding the molecular mechanisms of excitation-contraction-coupling remodeling in the fibrillating human atria is important to identify new potential targets for AF therapy
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