561 research outputs found

    Broadband noise decoherence in solid-state complex architectures

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    Broadband noise represents a severe limitation towards the implementation of a solid-state quantum information processor. Considering common spectral forms, we propose a classification of noise sources based on the effects produced instead of on their microscopic origin. We illustrate a multi-stage approach to broadband noise which systematically includes only the relevant information on the environment, out of the huge parametrization needed for a microscopic description. We apply this technique to a solid-state two-qubit gate in a fixed coupling implementation scheme.Comment: Proceedings of Nobel Symposium 141: Qubits for Future Quantum Informatio

    Effects of low-frequency noise cross-correlations in coupled superconducting qubits

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    We study the effects of correlated low frequency noise sources acting on a two qubit gate in a fixed coupling scheme. A phenomenological model for the spatial and cross-talk correlations is introduced. The decoherence inside the SWAP subspace is analysed by combining analytic results based on the adiabatic approximation and numerical simulations. Results critically depend on amplitude of the low frequency noise with respect to the qubits coupling strength. Correlations between noise sources induce qualitative different behaviors depending on the values of the above parameters. The possibility to reduce dephasing due to correlated low frequency noise by a recalibration protocol is discussed.Comment: 18 pages, 7 figure

    Role of the target orientation angle and orbital angular momentum in the evaporation residue production

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    The influence of the orientation angles of the target nucleus symmetry axis relative to the beam direction on the production of the evaporation residues is investigated for the 48^{48}Ca+154^{154}Sm reaction as a function of the beam energy. At low energies (Ec.m.<E_{\rm c.m.}<137 MeV), the yield of evaporation residues is observed only for collisions with small orientation angles (αT<450\alpha_T<45^0). At large energies (about Ec.m.=E_{\rm c.m.}=140--180 MeV) all the orientation angles αT\alpha_T can contribute to the evaporation residue cross section σER\sigma_{ER} in the 10--100 mb range, and at Ec.m.>E_{c.m.}>180 MeV σER\sigma_{ER} ranges around 0.1--10 mb because the fission barrier for a compound nucleus decreases by increasing its excitation energy and angular momentum.Comment: 20 pages, 10 figures, submitted to JPS

    Angular analysis of bremsstrahlung in alpha decay

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    A new quantum electrodynamical method of calculations of bremsstrahlung spectra in the α\alpha-decay of heavy nuclei taking into account the angle between the directions of α\alpha-particle motion (or its tunneling) and photon emission is presented. The angular bremsstrahlung spectra for 210Po^{210}{Po} have been obtained for the first time. According to calculations, the bremsstrahlung in the α\alpha-decay of this nucleus depends extremely weakly on the angle. Taking into account nuclear forces, such dependence is not changed visibly. An analytical formula of the angular dependence of the bremsstrahlung spectra is proposed and gives its harmonic behavior. The extremal values of the angle, at which the bremsstrahlung has maximal and minimal values, has been found.Comment: 15 pages, 1 file of figure in EPS format, LaTeX v.2e with EPJ style. In the new variant of the paper: 1) more attention is given to a convergence problem of computer calculations of the bremsstrahlung spectra; 2) a new section with inclusion of Woods-Saxon component in construction of the total realistic α\alpha-nucleus potential into our model (with our first brermsstrahlung spectra for 210Po^{210}{Po} at such potential) is included into the paper; 3) possible ways of further improvement of the quantum-mechanical models are pointed ou

    Bremsstrahlung in Alpha-Decay

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    We present the first fully quantum mechanical calculation of photon radiation accompanying charged particle decay from a barrier resonance. The soft-photon limit agrees with the classical results, but differences appear at next-to-leading-order. Under the conditions of alpha-decay of heavy nuclei, the main contribution to the photon emission stems from Coulomb acceleration and may be computed analytically. We find only a small contribution from the tunneling wave function under the barrier.Comment: 12 pages, 2 Postscript figure

    Design of a novel LOX-1 receptor antagonist mimicking the natural substrate

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    The lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1), the major receptor for oxidized low-density lipoprotein (ox-LDL) in endothelial cells, is overexpressed in atherosclerotic lesions. LOX-1 specific inhibitors, urgently necessary to reduce the rate of atherosclerotic and inflammation processes, are not yet available. We have designed and synthesized a new modified oxidized phospholipid, named PLAzPC, which plays to small scale the ligand-receptor recognition scheme. Molecular docking simulations confirm that PLAzPC disables the hydrophobic component of the ox-LDL recognition domain and allows the interaction of the l-lysine backbone charged groups with the solvent and with the charged/polar residues located around the edges of the LOX-1 hydrophobic tunnel. Binding assays, in a cell model system expressing human LOX-1 receptors, confirm that PLAzPC markedly inhibits ox-LDL binding to LOX-1 with higher efficacy compared to previously identified inhibitors

    Antiretroviral treatment efficacy after mutations reversion during T20 monotherapy, an alternative strategy in multi-failed HIV-1 infected patients

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    Purpose of the study Monotherapy maintenance with 3TC after multiple therapeutic failure, helps in maintaining the number of CD4, but, at the same time, slows down the speed of reversion of mutations usually achieved during complete interruption of therapy. Monotherapy with enfuvirtide (T20) can be an interesting alternative to 3TC monotherapy, due to the CD4-enhancement typical of this drug even during therapeutic failure. Aim of this study was to assess, in a proof-of-concept study, the efficacy of T20-monotherapy to maintain the levels of CD4, to allow reversal of mutations in the pol gene, and eventually to favor long-term success of subsequent HAART

    LANCL1 binds abscisic acid and stimulates glucose transport and mitochondrial respiration in muscle cells via the AMPK/PGC-1α/Sirt1 pathway

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    Objective: Abscisic acid (ABA) is a plant hormone also present and active in animals. In mammals, ABA regulates blood glucose levels by stimulating insulin-independent glucose uptake and metabolism in adipocytes and myocytes through its receptor LANCL2. The objective of this study was to investigate whether another member of the LANCL protein family, LANCL1, also behaves as an ABA receptor and, if so, which functional effects are mediated by LANCL1. Methods: ABA binding to human recombinant LANCL1 was explored by equilibrium-binding experiments with [3H]ABA, circular dichroism, and surface plasmon resonance. Rat L6 myoblasts overexpressing either LANCL1 or LANCL2, or silenced for the expression of both proteins, were used to investigate the basal and ABA-stimulated transport of a fluorescent glucose analog (NBDG) and the signaling pathway downstream of the LANCL proteins using Western blot and qPCR analysis. Finally, glucose tolerance and sensitivity to ABA were compared in LANCL2−/− and wild-type (WT) siblings. Results: Human recombinant LANCL1 binds ABA with a Kd between 1 and 10 μM, depending on the assay (i.e., in a concentration range that lies between the low and high-affinity ABA binding sites of LANCL2). In L6 myoblasts, LANCL1 and LANCL2 similarly, i) stimulate both basal and ABA-triggered NBDG uptake (4-fold), ii) activate the transcription and protein expression of the glucose transporters GLUT4 and GLUT1 (4-6-fold) and the signaling proteins AMPK/PGC-1α/Sirt1 (2-fold), iii) stimulate mitochondrial respiration (5-fold) and the expression of the skeletal muscle (SM) uncoupling proteins sarcolipin (3-fold) and UCP3 (12-fold). LANCL2−/− mice have a reduced glucose tolerance compared to WT. They spontaneously overexpress LANCL1 in the SM and respond to chronic ABA treatment (1 μg/kg body weight/day) with an improved glycemia response to glucose load and an increased SM transcription of GLUT4 and GLUT1 (20-fold) of the AMPK/PGC-1α/Sirt1 pathway and sarcolipin, UCP3, and NAMPT (4- to 6-fold). Conclusions: LANCL1 behaves as an ABA receptor with a somewhat lower affinity for ABA than LANCL2 but with overlapping effector functions: stimulating glucose uptake and the expression of muscle glucose transporters and mitochondrial uncoupling and respiration via the AMPK/PGC-1α/Sirt1 pathway. Receptor redundancy may have been advantageous in animal evolution, given the role of the ABA/LANCL system in the insulin-independent stimulation of cell glucose uptake and energy metabolism
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