115 research outputs found

    Excessive Memory Usage of the ELLPACK Sparse Matrix Storage Scheme throughout the Finite Element Computations

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    Sparse matrices are occasionally encountered during solution of various problems by means of numerical methods, particularly the finite element method. ELLPACK sparse matrix storage scheme, one of the most widely used methods due to its implementation ease, is investigated in this study. The scheme uses excessive memory due to its definition. For the conventional finite element method, where the node elements are used, the excessive memory caused by redundant entries in the ELLPACK sparse matrix storage scheme becomes negligible for large scale problems. On the other hand, our analyses show that the redundancy is still considerable for the occasions where facet or edge elements have to be used

    Design of the Square Loop Frequency Selective Surfaces with Particle Swarm Optimization via the Equivalent Circuit Model

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    In this study, Particle Swarm Optimization is applied for the design of Square Loop Frequency Selective Surfaces (the conventional Square Loop, Gridded Square Loop, and Double Square Loop) via their equivalent circuits. For this purpose, first the derivation of the equivalent circuit formulation is revisited. Then an objective function, which is based on the transmission coefficients at various frequencies at the pass/stop-bands, is defined. By means of an ANSI C++ implementation, a platform independent console application (which depends on the Equivalent Circuit Models and continuous form of Particle Swarm Optimization) is developed. The obtained results are compared to those in the literature. It is observed that the Particle Swarm Optimization is perfectly suitable for this sort of problems, and the solution accuracy is limited to and dominated by that of the Equivalent Circuit Model

    Identification and functional analysis of an autophagy-related gene TdAtg8 in wild emmer wheat under biotic (fusarium culmorum) and abiotic (drought) stress conditions

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    Autophagy, literally self eating, is an evolutionary conserved catalytic process for vacuolar degradation of intracellular components, previously examined in yeast, mammals and plants. Abiotic stress factors, including nutrient starvation, oxidative stress, salt stress and osmotic stress have been previously reported to induce autophagy in plants. In this study, for the first time, Atg8 gene was cloned from wild emmer wheat (TdAtg8) and the role of autophagy under biotic and abiotic stress conditions was investigated. Examination of TdAtg8 expression patterns indicates that Atg8 expression was immensely upregulated under drought stress, especially in the roots. Monodansylcadaverine (MDC) and Lysotracker Red markers utilized to observe autophagosomes revealed that autophagy is constitutively active in T. dicoccoides. Moreover, autophagy was determined to be more active in plants exposed to drought stress when compared to plants grown under normal conditions. TdAtg8 gene was demonstrated to complement Atg8 yeast mutants grown under starvation conditions in a drop test assay. For further functional analysis, ATG8 protein from T. dicoccoides were expressed in yeast and analyzed with western blotting. TdAtg8 was also silenced in wild emmer wheat by virus-induced gene silencing and its role was investigated in the presence of a plant pathogen, Fusarium culmorum. This response, for the first time, showed that fungi sporulation decreased in Atg8 silenced plants in comparison to controls. Based on the data obtained, we conclude that the plants become more resistant against the plant pathogen when the autophagy was inhibited

    Sub-wavelength imaging with a left-handed material flat lens

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    We study numerically, by means of the pseudospectral time-domain method, the unique features of imaging by a flat lens made of a left-handed metamaterial that possesses the property of negative refraction. We confirm the earlier finding that a left-handed flat lens can provide near-perfect imaging of a point source and a pair of point sources with clear evidence of the sub-wavelength resolution. We illustrate the limitation of the resolution in the time-integrated image due to the presence of surface waves.Comment: 4 pages, RevTeX, 6 figures; added references and some discussio

    Eukaryotic translation initiation factor 4All contributes to microRNA-122 regulation of hepatitis C virus replication

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    Hepatitis C virus (HCV) is a positive sense RNA virus that persistently infects human liver, leading to cirrhosis and hepatocellular carcinoma. HCV replication requires the liver-specific microRNA-122 (miR-122). In contrast to canonical miRNA-mediated repression via 3’UTR sites, miR-122 positively regulates HCV replication by a direct interaction with the 5’ untranslated region (UTR) of the viral RNA. The protein factor requirements for this unusual miRNA regulation remain poorly understood. Here, we identify eIF4AII, previously implicated in miRNA-mediated repression via 3’UTR sites, as a host factor that is important for HCV replication. We demonstrate that eIF4AII interacts with HCV RNA and that this interaction is miR-122-dependent. We show that effective miR-122 binding to, and regulation of, HCV RNA are reduced following eIF4AII depletion. We find that the previously identified HCV co-factor CNOT1, which has also been implicated in miRNA-mediated repression via 3’UTR sites, contributes to regulation of HCV by eIF4AII. Finally, we show that eIF4AI knockdown alleviates the inhibition of HCV replication mediated by depletion of either eIF4AII or CNOT1. Our results suggest a competition effect between the eIF4A proteins to influence HCV replication by modulation of miR-122 function

    A SARS-CoV-2 protein interaction map reveals targets for drug repurposing

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    The novel coronavirus SARS-CoV-2, the causative agent of COVID-19 respiratory disease, has infected over 2.3 million people, killed over 160,000, and caused worldwide social and economic disruption1,2. There are currently no antiviral drugs with proven clinical efficacy, nor are there vaccines for its prevention, and these efforts are hampered by limited knowledge of the molecular details of SARS-CoV-2 infection. To address this, we cloned, tagged and expressed 26 of the 29 SARS-CoV-2 proteins in human cells and identified the human proteins physically associated with each using affinity-purification mass spectrometry (AP-MS), identifying 332 high-confidence SARS-CoV-2-human protein-protein interactions (PPIs). Among these, we identify 66 druggable human proteins or host factors targeted by 69 compounds (29 FDA-approved drugs, 12 drugs in clinical trials, and 28 preclinical compounds). Screening a subset of these in multiple viral assays identified two sets of pharmacological agents that displayed antiviral activity: inhibitors of mRNA translation and predicted regulators of the Sigma1 and Sigma2 receptors. Further studies of these host factor targeting agents, including their combination with drugs that directly target viral enzymes, could lead to a therapeutic regimen to treat COVID-19
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