282 research outputs found

    Dynamics of transmission in disordered topological insulators

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    Here we show in simulations of the Haldane model that pulse propagation in disordered topological insulators is robust throughout the central portion of the band gap where localized modes do not arise. Since transmission is robust in topological insulators, the essential field variable is the phase of the transmitted field, or, equivalently, its spectral derivative, which is the transmission time. Except near resonances with bulk localized modes that couple the upper and lower edges of a topological insulator, the transmission time in a topological insulator is proportional to the density of states and to the energy excited within the sample. The average transmission time is enhanced in disordered TIs near the band edge and slightly suppressed in the center of the band gap. The variance of the transmission time at the band edge for a random ensemble with moderate disorder is dominated by fluctuations at resonances with localized states, and initially scales quadratically. When modes are absent, such as in the center of the band gap, the transmission time self-averages and its variance scales linearly. This leads to significant sample-to-sample fluctuations in the transmission time. However, because the transmission time is the sum of contributions from the continuum edge mode, which stretches across the band gap, and far-off-resonance modes near the band edge, there are no sharp features in the spectrum of transmission time in the center of the band gap. As a result, ultrashort, broadband pulses are faithfully transmitted in the center of the band gap of topological insulators with moderate disorder and bent paths. This allows for robust signal propagation in complex topological metawaveguides for applications in high-speed optoelectronics and telecommunications

    Spin Gap and Resonance at the Nesting Wavevector in Superconducting FeSe0.4Te0.6

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    Neutron scattering is used to probe magnetic excitations in FeSe_{0.4}Te_{0.6} (T_c=14 K). Low energy spin fluctuations are found with a characteristic wave vector (0.5,0.5,L)(0.5,0.5,L) that corresponds to Fermi surface nesting and differs from Q_m=(\delta,0,0.5) for magnetic ordering in Fe_{1+y}Te. A spin resonance with \hbar\Omega_0=6.5 meV \approx 5.3 k_BT_c and \hbar\Gamma=1.25 meV develops in the superconducting state from a normal state continuum. We show that the resonance is consistent with a bound state associated with s+/- superconductivity and imperfect quasi-2D Fermi surface nesting.Comment: 4 pages, 4 figures, Submitted to Phys. Rev. Let

    A Comparative Study on Viewers’ Perceptions of the Portrait of the MH370 Incident by the Social Media in Malaysia and China

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    The MH370 incident demonstrated an unprecedented international humanitarian response from the technology sector. This study attempted to have a deep insight about online users’ perceptions towards the portrait of this incident by the social media in Malaysia and China. Social networking sites such as Facebook (in Malaysia), Weibo (in China) and Wechat (in China), become the public opinion field that illustrates sorts of openness and negotiation in Malaysia and China. This study argued the technical and social knowledge to work with social media represents a steep learning curve for crisis managers who are used to working with traditional new media, as there is a significant relationship between empowerment of social media and effectiveness of crisis communication. The result of survey indicated different level of engagement with the content posted on social media in these two countries. This study proposes social media strategies that will be an integral part of any organization’s plan to respond to an accident or major incident

    Invariance principle for wave propagation inside inhomogeneously disordered materials

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    Disorder is more the rule than the exception in natural and synthetic materials. Nonetheless, wave propagation within inhomogeneously disordered materials has received scant attention. We combine microwave experiments and theory to find the spatial variation of generic wave propagation quantities in inhomogeneously disordered materials. We demonstrate that wave statistics within samples of any dimension are independent of the detailed structure of a material and depend only on the net strengths of distributed scattering and reflection between the observation point and each of the boundaries.Comment: main: 6 pages, 4 figures; Supplemental materials: 13 pages, 4 figure

    Janus monolayers of transition metal dichalcogenides.

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    Structural symmetry-breaking plays a crucial role in determining the electronic band structures of two-dimensional materials. Tremendous efforts have been devoted to breaking the in-plane symmetry of graphene with electric fields on AB-stacked bilayers or stacked van der Waals heterostructures. In contrast, transition metal dichalcogenide monolayers are semiconductors with intrinsic in-plane asymmetry, leading to direct electronic bandgaps, distinctive optical properties and great potential in optoelectronics. Apart from their in-plane inversion asymmetry, an additional degree of freedom allowing spin manipulation can be induced by breaking the out-of-plane mirror symmetry with external electric fields or, as theoretically proposed, with an asymmetric out-of-plane structural configuration. Here, we report a synthetic strategy to grow Janus monolayers of transition metal dichalcogenides breaking the out-of-plane structural symmetry. In particular, based on a MoS2 monolayer, we fully replace the top-layer S with Se atoms. We confirm the Janus structure of MoSSe directly by means of scanning transmission electron microscopy and energy-dependent X-ray photoelectron spectroscopy, and prove the existence of vertical dipoles by second harmonic generation and piezoresponse force microscopy measurements

    A Conformation-Sensitive Monoclonal Antibody against the A2 Domain of von Willebrand Factor Reduces Its Proteolysis by ADAMTS13

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    The size of von Willebrand factor (VWF), controlled by ADAMTS13-dependent proteolysis, is associated with its hemostatic activity. Many factors regulate ADAMTS13-dependent VWF proteolysis through their interaction with VWF. These include coagulation factor VIII, platelet glycoprotein 1bα, and heparin sulfate, which accelerate the cleavage of VWF. Conversely, thrombospondin-1 decreases the rate of VWF proteolysis by ADAMTS13 by competing with ADAMTS13 for the A3 domain of VWF. To investigate whether murine monoclonal antibodies (mAbs) against human VWF affect the susceptibility of VWF to proteolysis by ADAMTS13 in vitro, eight mAbs to different domains of human VWF were used to evaluate the effects on VWF cleavage by ADAMTS13 under fluid shear stress and static/denaturing conditions. Additionally, the epitope of anti-VWF mAb (SZ34) was mapped using recombinant proteins in combination with enzyme-linked immunosorbent assay and Western blot analysis. The results indicate that mAb SZ34 inhibited proteolytic cleavage of VWF by ADAMTS13 in a concentration-dependent manner under fluid shear stress, but not under static/denaturing conditions. The binding epitope of SZ34 mAb is located between A1555 and G1595 in the central A2 domain of VWF. These data show that an anti-VWF mAb against the VWF-A2 domain (A1555-G1595) reduces the proteolytic cleavage of VWF by ADAMTS13 under shear stress, suggesting the role of this region in interaction with ADAMTS13

    Susceptibility of HIV-1 Subtypes B′, CRF07_BC and CRF01_AE that Are Predominantly Circulating in China to HIV-1 Entry Inhibitors

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    The B', CRF07_BC and CRF01_AE are the predominant HIV-1 subtypes in China. It is essential to determine their baseline susceptibility to HIV entry inhibitors before these drugs are used in China.The baseline susceptibility of 14 representative HIV-1 isolates (5 CRF07_BC, 4 CRF01_AE, and 5 B'), most of which were R5 viruses, obtained from drug-naïve patients to HIV entry inhibitors, including two fusion inhibitors (enfuvirtide and C34), two CCR5 antagonists (maraviroc and TAK779) and one CXCR4 antagonist (AMD3100), were determined by virus inhibition assay. The sequences of their env genes were amplified and analyzed. These isolates possessed similar susceptibility to C34, but they exhibited different sensitivity to enfuvirtide, maraviroc or TAK779. CRF07_BC isolates, which carried polymorphisms of A578T and V583I in the N-terminal heptad repeat and E630Q, E662A, K665S, A667K and S668N in the C-terminal heptad repeat of gp41, were about 5-fold less sensitive than B' and CRF01_AE isolates to enfuvirtide. Subtype B' isolates with a unique polymorphism site of F317W in V3 loop, were about 4- to 5-fold more sensitive than CRF07_BC and CRF01_AE isolates to maraviroc and TAK779. AMD3100 at the concentration as high as 5 µM exhibited no significant inhibitory activity against any of the isolates tested.Our results suggest that there are significant differences in baseline susceptibility to HIV entry inhibitors among the predominant HIV-1 subtypes in China and the differences may partly result from the naturally occurring polymorphisms in these subtypes. This study provides useful information for rational design of optimal therapeutic regimens for HIV-1-infected patients in China

    Extensive Crosstalk between O-GlcNAcylation and Phosphorylation Regulates Akt Signaling

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    O-linked N-acetylglucosamine glycosylations (O-GlcNAc) and O-linked phosphorylations (O-phosphate), as two important types of post-translational modifications, often occur on the same protein and bear a reciprocal relationship. In addition to the well documented phosphorylations that control Akt activity, Akt also undergoes O-GlcNAcylation, but the interplay between these two modifications and the biological significance remain unclear, largely due to the technique challenges. Here, we applied a two-step analytic approach composed of the O-GlcNAc immunoenrichment and subsequent O-phosphate immunodetection. Such an easy method enabled us to visualize endogenous glycosylated and phosphorylated Akt subpopulations in parallel and observed the inhibitory effect of Akt O-GlcNAcylations on its phosphorylation. Further studies utilizing mass spectrometry and mutagenesis approaches showed that O-GlcNAcylations at Thr 305 and Thr 312 inhibited Akt phosphorylation at Thr 308 via disrupting the interaction between Akt and PDK1. The impaired Akt activation in turn resulted in the compromised biological functions of Akt, as evidenced by suppressed cell proliferation and migration capabilities. Together, this study revealed an extensive crosstalk between O-GlcNAcylations and phosphorylations of Akt and demonstrated O-GlcNAcylation as a new regulatory modification for Akt signaling
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