Controlled and combined remote implementations of partially unknown quantum operations of multiqubits using GHZ states

We propose and prove protocols of controlled and combined remote implementations of partially unknown quantum operations belonging to the restricted sets [An Min Wang: PRA, \textbf{74}, 032317(2006)] using GHZ states. We detailedly describe the protocols in the cases of one qubit, respectively, with one controller and with two senders. Then we extend the protocols to the cases of multiqubits with many controllers and two senders. Because our protocols have to demand the controller(s)'s startup and authorization or two senders together working and cooperations, the controlled and combined remote implementations of quantum operations definitely can enhance the security of remote quantum information processing and potentially have more applications. Moreover, our protocol with two senders is helpful to farthest arrive at the power of remote implementations of quantum operations in theory since the different senders perhaps have different operational resources and different operational rights in practice.Comment: 26 pages, the submitted versio

Scheme for remote implementation of partially unknown quantum operation of two qubits in cavity QED

By constructing the recovery operations of the protocol of remote implementation of partially unknown quantum operation of two qubits [An Min Wang: PRA, \textbf{74}, 032317(2006)], we present a scheme to implement it in cavity QED. Long-lived Rydberg atoms are used as qubits, and the interaction between the atoms and the field of cavity is a nonresonant one. Finally, we analyze the experimental feasibility of this scheme.Comment: 7 pages, 2 figure

Pinning control of fractional-order weighted complex networks

In this paper, we consider the pinning control problem of fractional-order weighted complex dynamical networks. The well-studied integer-order complex networks are the special cases of the fractional-order ones. The network model considered can represent both directed and undirected weighted networks. First, based on the eigenvalue analysis and fractional-order stability theory, some local stability properties of such pinned fractional-order networks are derived and the valid stability regions are estimated. A surprising finding is that the fractional-order complex networks can stabilize itself by reducing the fractional-order q without pinning any node. Second, numerical algorithms for fractional-order complex networks are introduced in detail. Finally, numerical simulations in scale-free complex networks are provided to show that the smaller fractional-order q, the larger control gain matrix D, the larger tunable weight parameter , the larger overall coupling strength c, the more capacity that the pinning scheme may possess to enhance the control performance of fractional-order complex networks

Influence of an Sb doping layer in CIGS thin-film solar cells: a photoluminescence study

Sb doping of Cu(In,Ga)Se2 (CIGS) solar cells has been reported to exhibit a positive effect on the morphology of the absorber layer, offering a possibility to lower manufacturing cost by lowering the annealing temperatures during the CIGS deposition. In this work electron microscopy, energy-dispersive x-ray spectroscopy and photoluminescence experiments have been performed on cells deposited on soda-lime glass substrates, adding a thin Sb layer onto the Mo back contact prior to the CIGS absorber deposition. The defect structure of CIGS solar cells doped with Sb in this way has been investigated and is compared with that of undoped reference cells. The influence of substrate temperature during absorber growth has also been evaluated. For all samples the photoluminescence results can be explained by considering three donor–acceptor pair recombination processes involving the same defect pairs

Sulforaphane induces adipocyte browning and promotes glucose and lipid utilization

Scope: Obesity is closely related to the imbalance of white adipose tissue storing excess calories, and brown adipose tissue dissipating energy to produce heat in mammals. Recent studies revealed that acquisition of brown characteristics by white adipocytes, termed “browning,” may positively contribute to cellular bioenergetics and metabolism homeostasis. The goal was to investigate the putative effects of natural antioxidant sulforaphane (1-isothiocyanate-4-methyl-sulfonyl butane; SFN) on browning of white adipocytes. Methods and Results: 3T3-L1 mature white adipocytes were treated with SFN for 48 h, and then the mitochondrial content, function, and energy utilization were assessed. SFN was found to induce 3T3-L1 adipocytes browning based on the increased mitochondrial content and activity of respiratory chain enzymes, whereas the mechanism involved the upregulation of nuclear factor E2-related factor 2/ sirtuin1/ peroxisome proliferator-activated receptor gamma coactivator 1 alpha signaling. SFN enhanced uncoupling protein 1 expression, a marker for brown adipocyte, leading to the decrease in cellular ATP. SFN also enhanced glucose uptake and oxidative utilization, lipolysis and fatty acid oxidation in 3T3-L1 adipocytes. Conclusion: SFN-induced browning of white adipocytes enhanced the utilization of cellular fuel, and the application of SFN is a promising strategy to combat obesity and obesity-related metabolic disorder

Generic Constraints on the Relativistic Mean-Field and Skyrme-Hartree-Fock Models from the Pure Neutron Matter Equation of State

We study the nuclear symmetry energy S(rho) and related quantities of nuclear physics and nuclear astrophysics predicted generically by relativistic mean-field (RMF) and Skyrme-Hartree-Fock (SHF) models. We establish a simple prescription for preparing equivalent RMF and SHF parametrizations starting from a minimal set of empirical constraints on symmetric nuclear matter, nuclear binding energy and charge radii, enforcing equivalence of their Lorenz effective masses, and then using the pure neutron matter (PNM) equation of state (EoS) obtained from ab-initio calculations to optimize the pure isovector parameters in the RMF and SHF models. We find the resulting RMF and SHF parametrizations give broadly consistent predictions of the symmetry energy J and its slope parameter L at saturation density within a tight range of <~2 MeV and <~6 MeV respectively, but that clear model dependence shows up in the predictions of higher-order symmetry energy parameters, leading to important differences in (a) the slope of the correlation between J and L from the confidence ellipse, (b) the isospin-dependent part of the incompressibility of nuclear matter K_tau, (c) the symmetry energy at supra-saturation densities, and (d) the predicted neutron star radii. The model dependence can lead to about 1-2 km difference in predictions of the neutron star radius given identical predicted values of J, L and symmetric nuclear matter (SNM) saturation properties. Allowing the full freedom in the effective masses in both models leads to constraints of 30<~J<~31.5 MeV, 35<~L<~60 MeV, -330<~K_tau<~-216 MeV for the RMF model as a whole and 30<~J<~33 MeV, 28<~L<~65 MeV, -420<~K_tau<~-325 MeV for the SHF model as a whole. Notably, given PNM constraints, these results place RMF and SHF models as a whole at odds with some constraints on K_tau inferred from giant monopole resonance and neutron skin experimental results.Comment: 15 pages, 7 figures, 4 table

Lessons from LIMK1 enzymology and their impact on inhibitor design

LIM domain kinase 1 (LIMK1) is a key regulator of actin dynamics. It is thereby a potential therapeutic target for the prevention of fragile X syndrome and amyotrophic lateral sclerosis. Herein, we use X-ray crystallography and activity assays to describe how LIMK1 accomplishes substrate specificity, to suggest a unique ‘rock-and-poke’ mechanism of catalysis and to explore the regulation of the kinase by activation loop phosphorylation. Based on these findings, a differential scanning fluorimetry assay and a RapidFire mass spectrometry activity assay were established, leading to the discovery and confirmation of a set of small-molecule LIMK1 inhibitors. Interestingly, several of the inhibitors were inactive towards the closely related isoform LIMK2. Finally, crystal structures of the LIMK1 kinase domain in complex with inhibitors (PF-477736 and staurosporine, respectively) are presented, providing insights into LIMK1 plasticity upon inhibitor binding