5,906 research outputs found

    Stationary untrapped boundary conditions in general relativity

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    A class of boundary conditions for canonical general relativity are proposed and studied at the quasi-local level. It is shown that for untrapped or marginal surfaces, fixing the area element on the 2-surface (rather than the induced 2-metric) and the angular momentum surface density is enough to have a functionally differentiable Hamiltonian, thus providing definition of conserved quantities for the quasi-local regions. If on the boundary the evolution vector normal to the 2-surface is chosen to be proportional to the dual expansion vector, we obtain a generalization of the Hawking energy associated with a generalized Kodama vector. This vector plays the role for the stationary untrapped boundary conditions which the stationary Killing vector plays for stationary black holes. When the dual expansion vector is null, the boundary conditions reduce to the ones given by the non-expanding horizons and the null trapping horizons.Comment: 11 pages, improved discussion section, a reference added, accepted for publication in Classical and Quantum Gravit

    Ashtekar's New Variables and Positive Energy

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    We discuss earlier unsuccessful attempts to formulate a positive gravitational energy proof in terms of the New Variables of Ashtekar. We also point out the difficulties of a Witten spinor type proof. We then use the special orthonormal frame gauge conditions to obtain a locally positive expression for the New Variables Hamiltonian and thereby a ``localization'' of gravitational energy as well as a positive energy proof.Comment: 12 pages Plain Te

    The Hamiltonian boundary term and quasi-local energy flux

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    The Hamiltonian for a gravitating region includes a boundary term which determines not only the quasi-local values but also, via the boundary variation principle, the boundary conditions. Using our covariant Hamiltonian formalism, we found four particular quasi-local energy-momentum boundary term expressions; each corresponds to a physically distinct and geometrically clear boundary condition. Here, from a consideration of the asymptotics, we show how a fundamental Hamiltonian identity naturally leads to the associated quasi-local energy flux expressions. For electromagnetism one of the four is distinguished: the only one which is gauge invariant; it gives the familiar energy density and Poynting flux. For Einstein's general relativity two different boundary condition choices correspond to quasi-local expressions which asymptotically give the ADM energy, the Trautman-Bondi energy and, moreover, an associated energy flux (both outgoing and incoming). Again there is a distinguished expression: the one which is covariant.Comment: 12 pages, no figures, revtex

    Another positivity proof and gravitational energy localizations

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    Two locally positive expressions for the gravitational Hamiltonian, one using 4-spinors the other special orthonormal frames, are reviewed. A new quadratic 3-spinor-curvature identity is used to obtain another positive expression for the Hamiltonian and thereby a localization of gravitational energy and positive energy proof. These new results provide a link between the other two methods. Localization and prospects for quasi-localization are discussed.Comment: 14 pages REVTe

    An initial event in insect innate immune response: structural and biological studies of interactions between β-1,3-glucan and the N-terminal domain of β-1,3-glucan recognition protein

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    In response to invading microorganisms, insect β-1,3-glucan recognition protein (βGRP), a soluble receptor in the hemolymph, binds to the surfaces of bacteria and fungi and activates serine protease cascades that promote destruction of pathogens by means of melanization or expression of antimicrobial peptides. Here we report on the NMR solution structure of the N-terminal domain of βGRP (N-βGRP) from Indian meal moth (Plodia interpunctella), which is sufficient to activate the prophenoloxidase (proPO) pathway resulting in melanin formation. NMR and isothermal calorimetric titrations of N-βGRP with laminarihexaose, a glucose hexamer containing β-1,3 links, suggest a weak binding of the ligand. However, addition of laminarin, a glucose polysaccharide (~ 6 kDa) containing β-1,3 and β-1,6 links that activates the proPO pathway, to N-βGRP results in the loss of NMR cross-peaks from the backbone 15N-1H groups of the protein, suggesting the formation of a large complex. Analytical ultra centrifugation (AUC) studies of formation of N-βGRP:laminarin complex show that ligand-binding induces sel-fassociation of the protein:carbohydrate complex into a macro structure, likely containing six protein and three laminarin molecules (~ 102 kDa). The macro complex is quite stable, as it does not undergo dissociation upon dilution to sub-micromolar concentrations. The structural model thus derived from the present studies for N-βGRP:laminarin complex in solution differs from the one in which a single N-βGRP molecule has been proposed to bind to a triple helical form of laminarin on the basis of an X-ray crystallographic structure of N-βGRP:laminarihexaose complex [Kanagawa, M., Satoh, T., Ikeda, A., Adachi, Y., Ohno, N., and Yamaguchi, Y. (2011) J. Biol. Chem. 286, 29158-29165]. AUC studies and phenoloxidase activation measurements carried out with the designed mutants of N-βGRP indicate that electrostatic interactions involving Asp45, Arg54, and Asp68 between the ligand-bound protein molecules contribute in part to the stability of N-βGRP:laminarin macro complex and that a decreased stability is accompanied by a reduced activation of the proPO pathway. Increased β-1,6 branching in laminarin also results in destabilization of the macro complex. These novel findings suggest that ligand-induced self-association of βGRP:β-1,3-glucan complex may form a platform on a microbial surface for recruitment of downstream proteases, as a means of amplification of the initial signal of pathogen recognition for the activation of the proPO pathway

    Global evaluation of Doppler velocity errors of EarthCARE cloud-profiling radar using a global storm-resolving simulation

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    The cloud-profiling radar (CPR) on the Earth Clouds, Aerosol, and Radiation Explorer (EarthCARE) satellite (EC-CPR) is the first satellite-borne Doppler radar. In a previous study, we examined the effects of horizontal (along-track) integration and simple unfolding methods on the reduction of Doppler errors in the EC-CPR observations, and those effects were evaluated using two limited scenes in limited-latitude and low-pulse-repetition-frequency (PRF) settings. In this study, the amount of data used was significantly increased, and the area of the data used was extended globally. Not only low-PRF but also high-PRF settings were examined. We calculated the EC-CPR-observed Doppler velocity from pulse-pair covariances using the radar reflectivity factor and Doppler velocity obtained from a satellite data simulator and a global storm-resolving simulation. The global data were divided into five latitudinal zones, and each standard deviation of Doppler errors for 5 dBZe after 10 km integration was calculated. In the case of the low-PRF setting, the error without unfolding correction for the tropics reached a maximum of 2.2 m s−1 and then decreased toward the poles (0.43 m s−1). The error with unfolding correction for the tropics became much smaller at 0.63 m s−1. In the case of the high-PRF setting, the error without unfolding correction for the tropics reached a maximum of 0.78 m s−1 and then decreased toward the poles (0.19 m s−1). The error with unfolding correction for the tropics was 0.29 m s−1, less than half the value without the correction. The results of the analyses of the simulated data indicated that the zonal mean frequency of precipitation echoes was highest in the tropics and decreased toward the poles. Considering a limitation of the unfolding correction for discrimination between large upward velocity and large precipitation falling velocity, the latitudinal variation in the standard deviation of Doppler error can be explained by the precipitation echo distribution.</p

    Pim1 promotes human prostate cancer cell tumorigenicity and c-MYC transcriptional activity

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    <p>Abstract</p> <p>Background</p> <p>The serine/threonine kinase PIM1 has been implicated as an oncogene in various human cancers including lymphomas, gastric, colorectal and prostate carcinomas. In mouse models, Pim1 is known to cooperate with c-Myc to promote tumorigenicity. However, there has been limited analysis of the tumorigenic potential of Pim1 overexpression in benign and malignant human prostate cancer cells <it>in vivo</it>.</p> <p>Methods</p> <p>We overexpressed Pim1 in three human prostate cell lines representing different disease stages including benign (RWPE1), androgen-dependent cancer (LNCaP) and androgen-independent cancer (DU145). We then analyzed <it>in vitro </it>and <it>in vivo </it>tumorigenicity as well as the effect of Pim1 overexpression on c-MYC transcriptional activity by reporter assays and gene expression profiling using an inducible MYC-ER system. To validate that Pim1 induces tumorigenicity and target gene expression by modulating c-MYC transcriptional activity, we inhibited c-MYC using a small molecule inhibitor (10058-F4) or RNA interference.</p> <p>Results</p> <p>Overexpression of Pim1 alone was not sufficient to convert the benign RWPE1 cell to malignancy although it enhanced their proliferation rates when grown as xenografts <it>in vivo</it>. However, Pim1 expression enhanced the <it>in vitro </it>and <it>in vivo </it>tumorigenic potentials of the human prostate cancer cell lines LNCaP and DU145. Reporter assays revealed increased c-MYC transcriptional activity in Pim1-expressing cells and mRNA expression profiling demonstrated that a large fraction of c-MYC target genes were also regulated by Pim1 expression. The c-MYC inhibitor 10058-F4 suppressed the tumorigenicity of Pim1-expressing prostate cancer cells. Interestingly, 10058-F4 treatment also led to a reduction of Pim1 protein but not mRNA. Knocking-down c-MYC using short hairpin RNA reversed the effects of Pim1 on Pim1/MYC target genes.</p> <p>Conclusion</p> <p>Our results suggest an <it>in vivo </it>role of Pim1 in promoting prostate tumorigenesis although it displayed distinct oncogenic activities depending on the disease stage of the cell line. Pim1 promotes tumorigenicity at least in part by enhancing c-MYC transcriptional activity. We also made the novel discovery that treatment of cells with the c-MYC inhibitor 10058-F4 leads to a reduction in Pim1 protein levels.</p

    Search for Anisotropy of Ultra-High Energy Cosmic Rays with the Telescope Array Experiment

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    We study the anisotropy of Ultra-High Energy Cosmic Ray (UHECR) events collected by the Telescope Array (TA) detector in the first 40 months of operation. Following earlier studies, we examine event sets with energy thresholds of 10 EeV, 40 EeV, and 57 EeV. We find that the distributions of the events in right ascension and declination are compatible with an isotropic distribution in all three sets. We then compare with previously reported clustering of the UHECR events at small angular scales. No significant clustering is found in the TA data. We then check the events with E>57 EeV for correlations with nearby active galactic nuclei. No significant correlation is found. Finally, we examine all three sets for correlations with the large-scale structure of the Universe. We find that the two higher-energy sets are compatible with both an isotropic distribution and the hypothesis that UHECR sources follow the matter distribution of the Universe (the LSS hypothesis), while the event set with E>10 EeV is compatible with isotropy and is not compatible with the LSS hypothesis at 95% CL unless large deflection angles are also assumed. We show that accounting for UHECR deflections in a realistic model of the Galactic magnetic field can make this set compatible with the LSS hypothesis.Comment: 10 pages, 9 figure
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