39,416 research outputs found

    Search for Bc(ns)B_c(ns) via the Bc(ns)→Bc(ms)π+π−B_c(ns)\to B_c(ms)\pi^+\pi^- transition at LHCb and Z0Z_0 factory

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    It is interesting to study the characteristics of the whole family of BcB_c which contains two different heavy flavors. LHC and the proposed Z0Z^0 factory provide an opportunity because a large database on the BcB_c family will be achieved. BcB_c and its excited states can be identified via their decay modes. As suggested by experimentalists, Bc∗(ns)→Bc+γB_c^*(ns)\to B_c+\gamma is not easy to be clearly measured, instead, the trajectories of π+\pi^+ and π−\pi^- occurring in the decay of Bc(ns)→Bc(ms)+π+π−B_c(ns)\to B_c(ms)+\pi^+\pi^- (n>mn>m) can be unambiguously identified, thus the measurement seems easier and more reliable, therefore this mode is more favorable at early running stage of LHCb and the proposed Z0Z^0 factory. In this work, we calculate the rate of Bc(ns)→Bc(ms)+π+π−B_c(ns)\to B_c(ms)+\pi^+\pi^- in terms of the QCD multipole-expansion and the numerical results indicate that the experimental measurements with the luminosity of LHC and Z0Z^0 factory are feasible.Comment: 12 pages, 1 figures and 4 tables, acceptted by SCIENCE CHINA Physics, Mechanics & Astronomy (Science in China Series G

    Extraction of Plumes in Turbulent Thermal Convection

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    We present a scheme to extract information about plumes, a prominent coherent structure in turbulent thermal convection, from simultaneous local velocity and temperature measurements. Using this scheme, we study the temperature dependence of the plume velocity and understand the results using the equations of motion. We further obtain the average local heat flux in the vertical direction at the cell center. Our result shows that heat is not mainly transported through the central region but instead through the regions near the sidewalls of the convection cell.Comment: 4 pages, 4 figures, submitted to Physical Review Letter

    Orbital Interaction Mechanisms of Conductance Enhancement and Rectification by Dithiocarboxylate Anchoring Group

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    We study computationally the electron transport properties of dithiocarboxylate terminated molecular junctions. Transport properties are computed self-consistently within density functional theory and nonequilibrium Green's functions formalism. A microscopic origin of the experimentally observed current amplification by dithiocarboxylate anchoring groups is established. For the 4,4'-biphenyl bis(dithiocarboxylate) junction, we find that the interaction of the lowest unoccupied molecular orbital (LUMO) of the dithiocarboxylate anchoring group with LUMO and highest occupied molecular orbital (HOMO) of the biphenyl part results in bonding and antibonding resonances in the transmission spectrum in the vicinity of the electrode Fermi energy. A new microscopic mechanism of rectification is predicted based on the electronic structure of asymmetrical anchoring groups. We show that the peaks in the transmission spectra of 4'-thiolato-biphenyl-4-dithiocarboxylate junction respond differently to the applied voltage. Depending upon the origin of a transmission resonance in the orbital interaction picture, its energy can be shifted along with the chemical potential of the electrode to which the molecule is more strongly or more weakly coupled

    SUMO Modification Stabilizes Enterovirus 71 Polymerase 3D To Facilitate Viral Replication.

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    Accumulating evidence suggests that viruses hijack cellular proteins to circumvent the host immune system. Ubiquitination and SUMOylation are extensively studied posttranslational modifications (PTMs) that play critical roles in diverse biological processes. Cross talk between ubiquitination and SUMOylation of both host and viral proteins has been reported to result in distinct functional consequences. Enterovirus 71 (EV71), an RNA virus belonging to the family Picornaviridae, is a common cause of hand, foot, and mouth disease. Little is known concerning how host PTM systems interact with enteroviruses. Here, we demonstrate that the 3D protein, an RNA-dependent RNA polymerase (RdRp) of EV71, is modified by small ubiquitin-like modifier 1 (SUMO-1) both during infection and in vitro Residues K159 and L150/D151/L152 were responsible for 3D SUMOylation as determined by bioinformatics prediction combined with site-directed mutagenesis. Also, primer-dependent polymerase assays indicated that mutation of SUMOylation sites impaired 3D polymerase activity and virus replication. Moreover, 3D is ubiquitinated in a SUMO-dependent manner, and SUMOylation is crucial for 3D stability, which may be due to the interplay between the two PTMs. Importantly, increasing the level of SUMO-1 in EV71-infected cells augmented the SUMOylation and ubiquitination levels of 3D, leading to enhanced replication of EV71. These results together suggested that SUMO and ubiquitin cooperatively regulated EV71 infection, either by SUMO-ubiquitin hybrid chains or by ubiquitin conjugating to the exposed lysine residue through SUMOylation. Our study provides new insight into how a virus utilizes cellular pathways to facilitate its replication. IMPORTANCE: Infection with enterovirus 71 (EV71) often causes neurological diseases in children, and EV71 is responsible for the majority of fatalities. Based on a better understanding of interplay between virus and host cell, antiviral drugs against enteroviruses may be developed. As a dynamic cellular process of posttranslational modification, SUMOylation regulates global cellular protein localization, interaction, stability, and enzymatic activity. However, little is known concerning how SUMOylation directly influences virus replication by targeting viral polymerase. Here, we found that EV71 polymerase 3D was SUMOylated during EV71 infection and in vitro Moreover, the SUMOylation sites were determined, and in vitro polymerase assays indicated that mutations at SUMOylation sites could impair polymerase synthesis. Importantly, 3D is ubiquitinated in a SUMOylation-dependent manner that enhances the stability of the viral polymerase. Our findings indicate that the two modifications likely cooperatively enhance virus replication. Our study may offer a new therapeutic strategy against virus replication

    The magnetic dipole transitions in the (cbˉ)(c\bar{b}) binding system

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    The magnetic dipole transitions between the vector mesons Bc∗B_c^* and their relevant pseudoscalar mesons BcB_c (BcB_c, Bc∗B_c^*, Bc(2S)B_c(2S), Bc∗(2S)B_c^*(2S), Bc(3S)B_c(3S) and Bc∗(3S)B_c^*(3S) etc, the binding states of (cbˉ)(c\bar{b}) system) of the BcB_c family are interesting. To see the `hyperfine' splitting due to spin-spin interaction is an important topic for understanding the spin-spin interaction and the spectrum of the the (cbˉ)(c\bar{b}) binding system. The knowledge about the magnetic dipole transitions is also very useful for identifying the vector boson Bc∗B_c^* mesons experimentally, whose masses are just slightly above the masses of their relevant pseudoscalar mesons BcB_c accordingly. Considering the possibility to observe the vector mesons via the transitions at Z0Z^0 factory and the potentially usages of the theoretical estimate on the transitions, we fucus our efforts on calculating the magnetic dipole transitions, i.e. precisely to calculate the rates for the transitions such as decays Bc∗→BcγB_c^*\to B_c\gamma and Bc∗→Bce+e−B_c^*\to B_c e^+e^-, and particularly work in the Behte-Salpeter framework. In the estimate, as a typical example, we carefully investigate the dependance of the rate Γ(Bc∗→Bcγ)\Gamma(B_c^*\to B_c\gamma) on the mass difference ΔM=MBc∗−MBc\Delta M=M_{B_c^*}-M_{B_c} as well.Comment: 10 pages, 2 figures, 1 tabl
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