Enhanced electron correlations in the new binary stannide PdSn4: a homologue of the Dirac nodal arc semimetal PtSn4

The advent of nodal-line semi-metals, i.e. systems in which the conduction and valence bands cross each other along a closed trajectory (line or loop) inside the Brillouin zone, has opened up a new arena for the exploration of topological condensed matter in which, due to a vanishing density of states near the Fermi level, electron correlation effects may also play an important role. In spite of this conceptual richness however, material realization of nodal-line (loop) fermions is rare, with PbTaSe2, ZrSiS and PtSn4 the only promising known candidates. Here we report the synthesis and physical properties of a new compound PdSn4 that is isostructural with PtSn4 yet possesses quasiparticles with significantly enhanced effective masses. In addition, PdSn4 displays an unusual polar angular magnetoresistance which at a certain field orientation, varies linearly with field up to 55 Tesla. Our study suggests that, in association with its homologue PtSn4 whose low-lying excitations were recently claimed to possess Dirac node arcs, PdSn4 may be a promising candidate in the search for novel topological states with enhanced correlation effects.Comment: 6 figures, 1 tabl

Ultra-bright, ultra-broadband hard x-ray driven by laser-produced energetic electron beams

We propose a new method of obtaining a compact ultra-bright, ultra-broadband hard X-ray source. This X-ray source has a high peak brightness in the order of 1022 photons/(s mm2 mrad2 0.1\%BW), an ultrashort duration (10 fs), and a broadband spectrum (flat distribution from 0.1 MeV to 4 MeV), and thus has wide-ranging potential applications, such as in ultrafast Laue diffraction experiments. In our scheme, laser-plasma accelerators (LPAs) provide driven electron beams. A foil target is placed oblique to the beam direction so that the target normal sheath field (TNSF) is used to provide a bending force. Using this TNSF-kick scheme, we can fully utilize the advantages of current LPAs, including their high charge, high energy, and low emittance

Glycomics Analysis of Mammalian Heparan Sulfates Modified by the Human Extracellular Sulfatase HSulf2

The Sulfs are a family of endosulfatases that selectively modify the 6O-sulfation state of cell-surface heparan sulfate (HS) molecules. Sulfs serve as modulators of cell-signaling events because the changes they induce alter the cell surface co-receptor functions of HS chains. A variety of studies have been aimed at understanding how Sulfs modify HS structure, and many of these studies utilize Sulf knockout cell lines as the source for the HS used in the experiments. However, genetic manipulation of Sulfs has been shown to alter the expression levels of HS biosynthetic enzymes, and in these cases an assessment of the fine structural changes induced solely by Sulf enzymatic activity is not possible. Therefore, the present work aims to extend the understanding of substrate specificities of HSulf2 using in vitro experiments to compare HSulf2 activities on HS from different organ tissues.To further the understanding of Sulf enzymatic activity, we conducted in vitro experiments where a variety of mammalian HS substrates were modified by recombinant human Sulf2 (HSulf2). Subsequent to treatment with HSulf2, the HS samples were exhaustively depolymerized and analyzed using size-exclusion liquid chromatography-mass spectrometry (SEC-LC/MS). We found that HSulf2 activity was highly dependent on the structural features of the HS substrate. Additionally, we characterized, for the first time, the activity of HSulf2 on the non-reducing end (NRE) of HS chains. The results indicate that the action pattern of HSulf2 at the NRE is different compared to internally within the HS chain.The results of the present study indicate that the activity of Sulfs is dependent on the unique structural features of the HS populations that they edit. The activity of HSulf2 at HS NREs implicates the Sulfs as key regulators of this region of the chains, and concomitantly, the protein-binding events that occur there

Effects of Exogenous Galanin on Neuropathic Pain State and Change of Galanin and Its Receptors in DRG and SDH after Sciatic Nerve-Pinch Injury in Rat

A large number of neuroanatomical, neurophysiologic, and neurochemical mechanisms are thought to contribute to the development and maintenance of neuropathic pain. However, mechanisms responsible for neuropathic pain have not been completely delineated. It has been demonstrated that neuropeptide galanin (Gal) is upregulated after injury in the dorsal root ganglion (DRG) and spinal dorsal horn (SDH) where it plays a predominantly antinociceptive role. In the present study, sciatic nerve-pinch injury rat model was used to determine the effects of exogenous Gal on the expression of the Gal and its receptors (GalR1, GalR2) in DRG and SDH, the alterations of pain behavior, nerve conduction velocity (NCV) and morphology of sciatic nerve. The results showed that exogenous Gal had antinociceptive effects in this nerve-pinch injury induced neuropathic pain animal model. It is very interesting that Gal, GalR1 and GalR2 change their expression greatly in DRG and SDH after nerve injury and intrathecal injection of exougenous Gal. Morphological investigation displays a serious damage after nerve-pinch injury and an amendatory regeneration after exogenous Gal treatment. These findings imply that Gal, via activation of GalR1 and/or GalR2, may have neuroprotective effects in reducing neuropathic pain behaviors and improving nerve regeneration after nerve injury