29 research outputs found

    Ising Universality in Three Dimensions: A Monte Carlo Study

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    We investigate three Ising models on the simple cubic lattice by means of Monte Carlo methods and finite-size scaling. These models are the spin-1/2 Ising model with nearest-neighbor interactions, a spin-1/2 model with nearest-neighbor and third-neighbor interactions, and a spin-1 model with nearest-neighbor interactions. The results are in accurate agreement with the hypothesis of universality. Analysis of the finite-size scaling behavior reveals corrections beyond those caused by the leading irrelevant scaling field. We find that the correction-to-scaling amplitudes are strongly dependent on the introduction of further-neighbor interactions or a third spin state. In a spin-1 Ising model, these corrections appear to be very small. This is very helpful for the determination of the universal constants of the Ising model. The renormalization exponents of the Ising model are determined as y_t = 1.587 (2), y_h = 2.4815 (15) and y_i = -0.82 (6). The universal ratio Q = ^2/ is equal to 0.6233 (4) for periodic systems with cubic symmetry. The critical point of the nearest-neighbor spin-1/2 model is K_c=0.2216546 (10).Comment: 25 pages, uuencoded compressed PostScript file (to appear in Journal of Physics A

    Human Herpesvirus 8 Interferon Regulatory Factor-Mediated BH3-Only Protein Inhibition via Bid BH3-B Mimicry

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    Viral replication efficiency is in large part governed by the ability of viruses to counteract pro-apoptotic signals induced by infection of host cells. For HHV-8, viral interferon regulatory factor-1 (vIRF-1) contributes to this process in part via inhibitory interactions with BH3-only protein (BOP) Bim, recently identified as an interaction partner of vIRF-1. Here we recognize that the Bim-binding domain (BBD) of vIRF-1 resembles a region (BH3-B) of Bid, another BOP, which interacts intramolecularly with the functional BH3 domain of Bid to inhibit it pro-apoptotic activity. Indeed, vIRF-1 was found to target Bid in addition to Bim and to interact, via its BBD region, with the BH3 domain of each. In functional assays, BBD could substitute for BH3-B in the context of Bid, to suppress Bid-induced apoptosis in a BH3-binding-dependent manner, and vIRF-1 was able to protect transfected cells from apoptosis induced by Bid. While vIRF-1 can mediate nuclear sequestration of Bim, this was not the case for Bid, and inhibition of Bid and Bim by vIRF-1 could occur independently of nuclear localization of the viral protein. Consistent with this finding, direct BBD-dependent inactivation by vIRF-1 of Bid-induced mitochondrial permeabilization was demonstrable in vitro and isolated BBD sequences were also active in this assay. In addition to Bim and Bid BH3 domains, BH3s of BOPs Bik, Bmf, Hrk, and Noxa also were found to bind BBD, while those of both pro- and anti-apoptotic multi-BH domain Bcl-2 proteins were not. Finally, the significance of Bid to virus replication was demonstrated via Bid-depletion in HHV-8 infected cells, which enhanced virus production. Together, our data demonstrate and characterize BH3 targeting and associated inhibition of BOP pro-apoptotic activity by vIRF-1 via Bid BH3-B mimicry, identifying a novel mechanism of viral evasion from host cell defenses

    The impact of marketing resources for initiation of children and the safety of troops in the paid sections Taekwondo

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    The article deals with the problem oforganizing and marketing features of the paid sports and sports services that provide educational complex. Presents the results of experimental work, a comparison of indicators of influence of advertising, PR in the process of initiation and security forces in the experimental group and control toll free group, the results of the survey conducted to identify the motives, to give children the previous 7-8 years, in the section on taekwondo and possible reasons for the refusal to deal with children in pai

    CONTACT PROBLEM FOR A TWO-LAYERED CYLINDER

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    Introduction.  The investigation of the contact problems  for cylindrical bodies is urgent due to the engineering contact strength analysis on shafts, cores and pipe-lines. In the present paper, a new contact problem of elastostatics on the interaction between a rigid band and an infinite two-layered cylinder, which consists of an internal continuous cylinder and an outer hollow one, with a frictionless contact between the cylinders, is studied. The outer cylindrical band of finite length is press fitted. By using a Fourier integral transformation, the problem is reduced to an integral equation with respect to the unknown contact pressure.Materials and Methods. Different combinations of linearly elastic materials of the composite cylinder are considered. Asymptotics of the symbol function of the integral equation kernel at zero and infinity is analyzed. This plays an important role for the application of the analytical solution methods. A key dimensionless geometric parameter is introduced, and a singular asymptotic technique is employed to solve the integral equation.Research Results. On the basis of the symbol function properties, a special easily factorable approximation being applicable in a wide variation range of the problem parameters is suggested. The Monte-Carlo method is used to determine the approximation parameters. The asymptotic formulas are derived both for the contact pressure, and for its integral characteristic. Calculations are made for different materials and for various relative thickness of the cylindrical layer  including thin-walled layers.Discussion and Conclusions. The asymptotic solutions are effective  for  relatively  wide  bands  when  the  contact  zone length is bigger than the diameter of the composite cylinder. It is significant that the method is applicable also for those cases when  the  outer  cylindrical  layer  is  treated  as  a  cylindrical shell. The asymptotic solutions can be recommended to engineers for the contact strength analysis of the elastic barrels with a flexible coating of another material

    Coordinated Expression of Tristetraprolin Post-Transcriptionally Attenuates Mitogenic Induction of the Oncogenic Ser/Thr Kinase Pim-1

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    <div><p>The serine/threonine kinase Pim-1 directs selected signaling events that promote cell growth and survival and is overexpressed in diverse human cancers. Pim-1 expression is tightly controlled through multiple mechanisms, including regulation of mRNA turnover. In several cultured cell models, mitogenic stimulation rapidly induced and stabilized <em>PIM1</em> mRNA, however, vigorous destabilization 4–6 hours later helped restore basal expression levels. Acceleration of <em>PIM1</em> mRNA turnover coincided with accumulation of tristetraprolin (TTP), an mRNA-destabilizing protein that targets transcripts containing AU-rich elements. TTP binds <em>PIM1</em> mRNA in cells, and suppresses its expression by accelerating mRNA decay. Reporter mRNA decay assays localized the TTP-regulated mRNA decay element to a discrete AU-rich sequence in the distal 3′-untranslated region that binds TTP. These data suggest that coordinated stimulation of TTP and <em>PIM1</em> expression limits the magnitude and duration of <em>PIM1</em> mRNA accumulation by accelerating its degradation as TTP protein levels increase. Consistent with this model, <em>PIM1</em> and TTP mRNA levels were well correlated across selected human tissue panels, and <em>PIM1</em> mRNA was induced to significantly higher levels in mitogen-stimulated fibroblasts from TTP-deficient mice. Together, these data support a model whereby induction of TTP mediates a negative feedback circuit to limit expression of selected mitogen-activated genes.</p> </div

    Decay kinetics of βG-<i>PIM1</i> chimeric mRNAs in transfected HeLa cells.

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    a<p>First-order constants (<i>k</i>) describing the decay kinetics of indicated βG-chimeric mRNAs were measured in HeLa/Tet-Off cells co-transfected with indicated expression plasmids by Dox time course assays as described under “<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0033194#s2" target="_blank">Materials and Methods</a>” and in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0033194#pone-0033194-g005" target="_blank">Figure 5</a>. mRNA half-lives were calculated using <i>t</i><sub>1/2</sub> = ln2/<i>k</i>. Quoted values represent the mean ± SD for <i>n</i> independent experiments.</p
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