11,762 research outputs found

    A Systemic Receptor Network Triggered by Human cytomegalovirus Entry

    Get PDF
    Virus entry is a multistep process that triggers a variety of cellular pathways interconnecting into a complex network, yet the molecular complexity of this network remains largely unsolved. Here, by employing systems biology approach, we reveal a systemic virus-entry network initiated by human cytomegalovirus (HCMV), a widespread opportunistic pathogen. This network contains all known interactions and functional modules (i.e. groups of proteins) coordinately responding to HCMV entry. The number of both genes and functional modules activated in this network dramatically declines shortly, within 25 min post-infection. While modules annotated as receptor system, ion transport, and immune response are continuously activated during the entire process of HCMV entry, those for cell adhesion and skeletal movement are specifically activated during viral early attachment, and those for immune response during virus entry. HCMV entry requires a complex receptor network involving different cellular components, comprising not only cell surface receptors, but also pathway components in signal transduction, skeletal development, immune response, endocytosis, ion transport, macromolecule metabolism and chromatin remodeling. Interestingly, genes that function in chromatin remodeling are the most abundant in this receptor system, suggesting that global modulation of transcriptions is one of the most important events in HCMV entry. Results of in silico knock out further reveal that this entire receptor network is primarily controlled by multiple elements, such as EGFR (Epidermal Growth Factor) and SLC10A1 (sodium/bile acid cotransporter family, member 1). Thus, our results demonstrate that a complex systemic network, in which components coordinating efficiently in time and space contributes to virus entry.Comment: 26 page

    Optimization of extraction condition for phytic acid from peanut meal by response surface methodology

    Get PDF
    Phytic acid (PA), a molecule with high commercial value, is one of the important component in peanutmeal. However, PA has not yet been isolated from peanut meal and played its role. This paper reportedthe extraction conditions of PA from peanut meal after removed protein. The independent variables werehydrochloric acid (HCl) concentration, solid to liquid ratio, extraction time and extraction temperature.Response surface methodology (RSM) was used to optimize the extraction conditions based on the extractionyield of PA. The results show that the second-order polynomial models derived from responseswell with the experimental (R2 = 0.9783). The optimal extraction condition was obtained with solid toliquid ratio of 1:16 (g:mL), HCl concentration of 0.02 mol/L, extraction time of 105 min, and extractiontemperature of 30 °C. At this condition, PA with higher purity were obtained. the extraction ratio was6.12%, and the content of PA was 182.7 mg/g dry PA extract. The experimental values under optimal conditionwere in good consistent with the predicted values. The PA extracted from peanut meal was verifiedqualitatively by IR spectra. The extraction technology of PA from peanut meal has a strong potential forrealized high-value utilization of peanut meal

    Distributed Consensus of Linear Multi-Agent Systems with Adaptive Dynamic Protocols

    Full text link
    This paper considers the distributed consensus problem of multi-agent systems with general continuous-time linear dynamics. Two distributed adaptive dynamic consensus protocols are proposed, based on the relative output information of neighboring agents. One protocol assigns an adaptive coupling weight to each edge in the communication graph while the other uses an adaptive coupling weight for each node. These two adaptive protocols are designed to ensure that consensus is reached in a fully distributed fashion for any undirected connected communication graphs without using any global information. A sufficient condition for the existence of these adaptive protocols is that each agent is stabilizable and detectable. The cases with leader-follower and switching communication graphs are also studied.Comment: 17 pages, 5 figue

    Top Quark Forward-Backward Asymmetry and Same-Sign Top Quark Pairs

    Full text link
    The top quark forward-backward asymmetry measured at the Tevatron collider shows a large deviation from standard model expectations. Among possible interpretations, a non-universal ZZ^\prime model is of particular interest as it naturally predicts a top quark in the forward region of large rapidity. To reproduce the size of the asymmetry, the couplings of the ZZ^\prime to standard model quarks must be large, inevitably leading to copious production of same-sign top quark pairs at the energies of the Large Hadron Collider (LHC). We explore the discovery potential for tttt and ttjttj production in early LHC experiments at 7-8 TeV and conclude that if {\it no} tttt signal is observed with 1 fb1^{-1} of integrated luminosity, then a non-universal ZZ^\prime alone cannot explain the Tevatron forward-backward asymmetry.Comment: Tevatron limit from same-sign tt search adde
    corecore