11,137 research outputs found

    FDTD analysis of the tunneling and growing exponential in a pair of epsilon-negative and mu-negative slabs

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    Pairing together material slabs with opposite signs for the real parts of their constitutive parameters has been shown to lead to interesting and unconventional properties that are not otherwise observable for single slabs. One such case was demonstrated analytically for the conjugate (i.e., complementary) pairing of infinite planar slabs of epsilon-negative (ENG) and mu-negative (MNG) media [A. Alu, and N. Engheta, IEEE Trans. Antennas Prop., 51, 2558 (2003)]. There it was shown that when these two slabs are juxtaposed and excited by an incident plane wave, resonance, complete tunneling, total transparency and reconstruction of evanescent waves may occur in the steady-state regime under a monochromatic excitation, even though each of the two slabs by itself is essentially opaque to the incoming radiation. This may lead to virtual imagers with sub-wavelength resolution and other anomalous phenomena overcoming the physical limit of diffraction. Here we explore how a transient sinusoidal signal that starts at t = 0 interacts with such an ENG-MNG pair of finite size using an FDTD technique. Multiple reflections and transmissions at each interface are shown to build up to the eventual steady state response of the pair, and during this process one can observe how the growing exponential phenomenon may actually occur inside this bilayer.Comment: 14 pages, 9 figures, submitted to Phys Rev

    Disruption of nNOS-NOS1AP protein-protein interactions suppresses neuropathic pain in mice

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    Elevated N-methyl-D-aspartate receptor (NMDAR) activity is linked to central sensitization and chronic pain. However, NMDAR antagonists display limited therapeutic potential because of their adverse side effects. Novel approaches targeting the NR2B-PSD95-nNOS complex to disrupt signaling pathways downstream of NMDARs show efficacy in preclinical pain models. Here, we evaluated the involvement of interactions between neuronal nitric oxide synthase (nNOS) and the nitric oxide synthase 1 adaptor protein (NOS1AP) in pronociceptive signaling and neuropathic pain. TAT-GESV, a peptide inhibitor of the nNOS-NOS1AP complex, disrupted the in vitro binding between nNOS and its downstream protein partner NOS1AP but not its upstream protein partner postsynaptic density 95 kDa (PSD95). Putative inactive peptides (TAT-cp4GESV and TAT-GESVΔ1) failed to do so. Only the active peptide protected primary cortical neurons from glutamate/glycine-induced excitotoxicity. TAT-GESV, administered intrathecally (i.t.), suppressed mechanical and cold allodynia induced by either the chemotherapeutic agent paclitaxel or a traumatic nerve injury induced by partial sciatic nerve ligation. TAT-GESV also blocked the paclitaxel-induced phosphorylation at Ser15 of p53, a substrate of p38 MAPK. Finally, TAT-GESV (i.t.) did not induce NMDAR-mediated motor ataxia in the rotarod test and did not alter basal nociceptive thresholds in the radiant heat tail-flick test. These observations support the hypothesis that antiallodynic efficacy of an nNOS-NOS1AP disruptor may result, at least in part, from blockade of p38 MAPK-mediated downstream effects. Our studies demonstrate, for the first time, that disrupting nNOS-NOS1AP protein-protein interactions attenuates mechanistically distinct forms of neuropathic pain without unwanted motor ataxic effects of NMDAR antagonists

    Optimizing Pulsar Timing Arrays to Maximize Gravitational Wave Single Source Detection: a First Cut

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    Pulsar Timing Arrays (PTAs) use high accuracy timing of a collection of low timing noise pulsars to search for gravitational waves in the microhertz to nanohertz frequency band. The sensitivity of such a PTA depends on (a) the direction of the gravitational wave source, (b) the timing accuracy of the pulsars in the array and (c) how the available observing time is allocated among those pulsars. Here, we present a simple way to calculate the sensitivity of the PTA as a function of direction of a single GW source, based only on the location and root-mean-square residual of the pulsars in the array. We use this calculation to suggest future strategies for the current North American Nanohertz Observatory for Gravitational Waves (NANOGrav) PTA in its goal of detecting single GW sources. We also investigate the affects of an additional pulsar on the array sensitivity, with the goal of suggesting where PTA pulsar searches might be best directed. We demonstrate that, in the case of single GW sources, if we are interested in maximizing the volume of space to which PTAs are sensitive, there exists a slight advantage to finding a new pulsar near where the array is already most sensitive. Further, the study suggests that more observing time should be dedicated to the already low noise pulsars in order to have the greatest positive effect on the PTA sensitivity. We have made a web-based sensitivity mapping tool available at http://gwastro.psu.edu/ptasm.Comment: 14 pages, 3 figures, accepted by Ap

    Branching, Capping, and Severing in Dynamic Actin Structures

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    Branched actin networks at the leading edge of a crawling cell evolve via protein-regulated processes such as polymerization, depolymerization, capping, branching, and severing. A formulation of these processes is presented and analyzed to study steady-state network morphology. In bulk, we identify several scaling regimes in severing and branching protein concentrations and find that the coupling between severing and branching is optimally exploited for conditions {\it in vivo}. Near the leading edge, we find qualitative agreement with the {\it in vivo} morphology.Comment: 4 pages, 2 figure

    Differential Uptake of Gold Nanoparticles by 2 Species of Tadpole, the Wood Frog (Lithobates Sylvaticus) and the Bullfrog (Lithobates Catesbeianus)

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    Engineered nanoparticles are aquatic contaminants of emerging concern that exert ecotoxicological effects on a wide variety of organisms. We exposed cetyltrimethylammonium bromide–capped spherical gold nanoparticles to wood frog and bullfrog tadpoles with conspecifics and in combination with the other species continuously for 21 d, then measured uptake and localization of gold. Wood frog tadpoles alone and in combination with bullfrog tadpoles took up significantly more gold than bullfrogs. Bullfrog tadpoles in combination with wood frogs took up significantly more gold than controls. The rank order of weight-normalized gold uptake was wood frogs in combination \u3e wood frogs alone \u3e bullfrogs in combination \u3e bullfrogs alone \u3e controls. In all gold-exposed groups of tadpoles, gold was concentrated in the anterior region compared with the posterior region of the body. The concentration of gold nanoparticles in the anterior region of wood frogs both alone and in combination with bullfrogs was significantly higher than the corresponding posterior regions. We also measured depuration time of gold in wood frogs. After 21 d in a solution of gold nanoparticles, tadpoles lost \u3e83% of internalized gold when placed in gold-free water for 5 d. After 10 d in gold-free water, tadpoles lost 94% of their gold. After 15 d, gold concentrations were below the level of detection. Our finding of differential uptake between closely related species living in similar habitats with overlapping geographical distributions argues against generalizing toxicological effects of nanoparticles for a large group of organisms based on measurements in only one species

    Branching, Capping, and Severing in Dynamic Actin Structures

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    Branched actin networks at the leading edge of a crawling cell evolve via protein-regulated processes such as polymerization, depolymerization, capping, branching, and severing. A formulation of these processes is presented and analyzed to study steady-state network morphology. In bulk, we identify several scaling regimes in severing and branching protein concentrations and find that the coupling between severing and branching is optimally exploited for conditions in vivo. Near the leading edge, we find qualitative agreement with the in vivo morphology

    A Parameter Study of the Dust and Gas Temperature in a Field of Young Stars

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    We model the thermal effect of young stars on their surrounding environment in order to understand clustered star formation. We take radiative heating of dust, dust-gas collisional heating, cosmic-ray heating, and molecular cooling into account. Using Dusty, a spherical continuum radiative transfer code, we model the dust temperature distribution around young stellar objects with various luminosities and surrounding gas and dust density distributions. We have created a grid of dust temperature models, based on our modeling with Dusty, which we can use to calculate the dust temperature in a field of stars with various parameters. We then determine the gas temperature assuming energy balance. Our models can be used to make large-scale simulations of clustered star formation more realistic.Comment: 29 pages, 19 figures. Submitted to Ap
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