Deutsches Elektronen-Synchrotron DESY

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    Search for supersymmetry in proton-proton collisions at s=\sqrt{s} = 13 TeV in events with high-momentum Z bosons and missing transverse momentum

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    A search for new physics in events with two highly Lorentz-boosted Z bosons and large missing transverse momentum is presented. The analyzed proton-proton collision data, corresponding to an integrated luminosity of 137 fb1^{-1}, were recorded at s=\sqrt{s}= 13 TeV by the CMS experiment at the CERN LHC. The search utilizes the substructure of jets with large radius to identify quark pairs from Z boson decays. Backgrounds from standard model processes are suppressed by requirements on the jet mass and the missing transverse momentum. No significant excess in the event yield is observed beyond the number of background events expected from the standard model. For a simplified supersymmetric model in which the Z bosons arise from the decay of gluinos, an exclusion limit of 1920 GeV on the gluino mass is set at 95% confidence level. This is the first search for beyond-standard-model production of pairs of boosted Z bosons plus large missing transverse momentum

    Towards Quantitative Interpretation of Fourier-Transform Photocurrent Spectroscopy on Thin-Film Solar Cells

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    The method of detecting deep defects in photovoltaic materials by Fourier-Transform Photocurrent Spectroscopy has gone through continuous development during the last two decades. Still, giving quantitative predictions of photovoltaic device performance is a challenging task. As new materials appear, a prediction of potentially achievable open-circuit voltage with respect to bandgap is highly desirable. From thermodynamics, a prediction can be made based on the radiative limit, neglecting non-radiative recombination and carrier transport effects. Beyond this, more accurate analysis has to be done. First, the absolute defect density has to be calculated, taking into account optical effects, such as absorption enhancement, due to scattering. Secondly, the electrical effect of thickness variation has to be addressed. We analyzed a series of state-of-the-art hydrogenated amorphous silicon solar cells of different thicknesses at different states of light soaking degradation. Based on a combination of empirical results with optical, electrical and thermodynamic simulations, we provide a predictive model of the open-circuit voltage of a device with a given defect density and absorber thickness. We observed that, rather than the defect density or thickness alone, it is their product or the total number of defects, that matters. Alternatively, including defect absorption into the thermodynamic radiative limit gives close upper bounds to the open-circuit voltage with the advantage of a much easier evaluation

    Measurement of the semileptonic Bˉ0D+ν\bar{B}^0 \to D^{*+} \ell^{-} \nu_{\ell} branching fraction with fully reconstructed BB meson decays and 34.6 fb1^{-1}of Belle II data

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    We present a first measurement of the B0ˉD+ν\bar{B^{0}} \rightarrow D^{*+} \ell^{-} \nu_{\ell} branching fraction using fully reconstructed BB meson decays employing the Full Event Interpretation algorithm. Collision events corresponding to an integrated luminosity of \lumi are analyzed, which were recorded by the Belle~II detector operated at the SuperKEKB accelerator complex. We measureB(B0ˉD+ν)=4.51±0.41stat±0.27syst±0.45πs\cal{B}(\bar{B^{0}} \rightarrow D^{*+} \ell^{-} \nu_{\ell}) =4.51 \pm 0.41_{stat}\pm0.27_{syst} \pm0.45_{\pi_s}, with the first and second error denoting the statistical and systematic uncertainty, respectively, and the third dominant uncertainty is from the slow pion reconstruction efficiency

    Preliminary Study for the Laboratory Experiment of Cosmic-Rays driven Magnetic Field Amplification

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    To understand astrophysical magnetic-field amplification, we conducted a feasibility study for a laboratory experiment of a non-resonant streaming instability at the Photo Injector Test Facility at DESY, Zeuthen site (PITZ). This non-resonant streaming instability, also known as Bell’s instability, is generally regarded as a candidate for the amplification of interstellar magnetic field in the upstream region of supernova-remnant shocks, which is crucial for the efficiency of diffusive shock acceleration. In the beam-plasma system composed of a radio-frequency electron gun and a gas-discharge plasma cell, the goal of our experiment is to demonstrate the development of the non-resonant streaming instability and to find its saturation level in the laboratory environment. Since we find that the electron beam will be significantly decelerated on account of an electrostatic streaming instability, which will decrease the growth rate of desired non-resonant streaming instability, we discuss possible ways to suppress the electrostatic streaming instability by considering the characteristics of a field-emission-based quasi continuous-wave electron beam

    Synchrotron X-ray fluorescence mapping of Ca, Sr and Zn at the neonatal line in human deciduous teeth reflects changing perinatal physiology

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    Objectives: Our first objective was to review the evidence describing the appearance and microstructure of theneonatal line in human deciduous teeth and to link this with known changes in neonatal physiology occurring atand around birth. A second objective was to explore ways to improve identification of the neonatal line bymapping the pre- and postnatal distribution of Ca, Sr and Zn in deciduous cuspal enamel and superimposingthese maps onto transmitted light micrographs that included a clear true section of the neonatal line.Materials and methods: We used synchrotron X-ray fluorescence to map elemental distributions in pre- andpostnatal enamel and dentine. Two deciduous canines and 5 deciduous molars were scanned with an X-ray beammonochromatised to 17.0 keV at either 10.0, 2.5 or 1.0 μm resolution and 10 ms integration time.Results: Calcium maps distinguished enamel and dentine but did not clearly demarcate tissues formed pre- orpostnatally. Strontium maps reflected presumed pre- and postnatal maternal serum levels and what are likely tobe diet-dependent regions of Sr enrichment or depletion. Prenatal Zn maps, particularly for dentine, mirrorelevated levels in the fetus and in colostrum during the first few days of life.Conclusions: The neonatal line, enamel dentine junction and surface enamel were all Zn-rich. Within the neonatalline Zn may be associated with increased crystallinity but also with caries resistance, both of which havebeen reported previously. Elemental mapping may improve the identification of ambiguous NNLs and so beuseful in forensic and archaeological studies

    AMPK and AKT protein kinases hierarchically phosphorylate the N-terminus of the FOXO1 transcription factor, modulating interactions with 14-3-3 proteins

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    Forkhead box protein O1 (FOXO1) is a transcription factor involved in various cellular processes such as glucose metabolism, development, stress resistance, and tumor suppression. FOXO1's transcriptional activity is controlled by different environmental cues through a myriad of posttranslational modifications. In response to growth factors, the serine/threonine kinase AKT phosphorylates Thr24^{24} and Ser256^{256} in FOXO1 to stimulate binding of 14-3-3 proteins, causing FOXO1 inactivation. In contrast, low nutrient and energy levels induce FOXO1 activity. AMP-activated protein kinase (AMPK), a master regulator of cellular energy homeostasis, partly mediates this effect through phosphorylation of Ser383^{383} and Thr649^{649} in FOXO1. In this study, we identified Ser22^{22} as an additional AMPK phosphorylation site in FOXO1's N terminus, with Ser22^{22} phosphorylation preventing binding of 14-3-3 proteins. The crystal structure of a FOXO1 peptide in complex with 14-3-3 σ at 2.3 Å resolution revealed that this is a consequence of both steric hindrance and electrostatic repulsion. Furthermore, we found that AMPK-mediated Ser22^{22}phosphorylation impairs Thr24^{24} phosphorylation by AKT in a hierarchical manner. Thus, numerous mechanisms maintain FOXO1 activity via AMPK signaling. AMPK-mediated Ser22^{22} phosphorylation directly and indirectly averts binding of 14-3-3 proteins, whereas phosphorylation of Ser383^{383} and Thr649^{649} complementarily stimulates FOXO1 activity. Our results shed light on a mechanism that integrates inputs from both AMPK and AKT signaling pathways in a small motif to fine-tune FOXO1 transcriptional activity

    Structural and Functional Characterization of NadR from Lactococcus lactis

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    NadR is a bifunctional enzyme that converts nicotinamide riboside (NR) into nicotinamide mononucleotide (NMN), which is then converted into nicotinamide adenine dinucleotide (NAD). Although a crystal structure of the enzyme from the Gram-negative bacterium Haemophilus influenzae is known, structural understanding of its catalytic mechanism remains unclear. Here, we purified the NadR enzyme from Lactococcus lactis and established an assay to determine the combined activity of this bifunctional enzyme. The conversion of NR into NAD showed hyperbolic dependence on the NR concentration, but sigmoidal dependence on the ATP concentration. The apparent cooperativity for ATP may be explained because both reactions catalyzed by the bifunctional enzyme (phosphorylation of NR and adenylation of NMN) require ATP. The conversion of NMN into NAD followed simple Michaelis-Menten kinetics for NMN, but again with the sigmoidal dependence on the ATP concentration. In this case, the apparent cooperativity is unexpected since only a single ATP is used in the NMN adenylyltransferase catalyzed reaction. To determine the possible structural determinants of such cooperativity, we solved the crystal structure of NadR from L. lactis (NadRLl). Co-crystallization with NAD, NR, NMN, ATP, and AMP-PNP revealed a ‘sink’ for adenine nucleotides in a location between two domains. This sink could be a regulatory site, or it may facilitate the channeling of substrates between the two domains

    Sjögren syndrome/scleroderma autoantigen 1 is a direct Tankyrase binding partner in cancer cells

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    Sjögren syndrome/scleroderma autoantigen 1 (SSSCA1) was first described as an auto-antigen over-expressed in Sjögren’s syndrome and in scleroderma patients. SSSCA1 has been linked to mitosis and centromere association and as a potential marker candidate in diverse solid cancers. Here we characterize SSSCA1 for the first time, to our knowledge, at the molecular, structural and subcellular level. We have determined the crystal structure of a zinc finger fold, a zinc ribbon domain type 2 (ZNRD2), at 2.3 Å resolution. We show that the C-terminal domain serves a dual function as it both behaves as the interaction site to Tankyrase 1 (TNKS1) and as a nuclear export signal. We identify TNKS1 as a direct binding partner of SSSCA1, map the binding site to TNKS1 ankyrin repeat cluster 2 (ARC2) and thus define a new binding sequence. We experimentally verify and map a new nuclear export signal sequence in SSSCA1

    Structural Studies of Glutamate Dehydrogenase (Isoform 1) From Arabidopsis thaliana, an Important Enzyme at the Branch-Point Between Carbon and Nitrogen Metabolism

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    Glutamate dehydrogenase (GDH) releases ammonia in a reversible NAD(P)+-dependent oxidative deamination of glutamate that yields 2-oxoglutarate (2OG). In current perception, GDH contributes to Glu homeostasis and plays a significant role at the junction of carbon and nitrogen assimilation pathways. GDHs are members of a superfamily of ELFV (Glu/Leu/Phe/Val) amino acid dehydrogenases and are subdivided into three subclasses, based on coenzyme specificity: NAD+-specific, NAD+/NADP+ dual-specific, and NADP+-specific. We determined in this work that the mitochondrial AtGDH1 isozyme from A. thaliana is NAD+-specific. Altogether, A. thaliana expresses three GDH isozymes (AtGDH1-3) targeted to mitochondria, of which AtGDH2 has an extra EF-hand motif and is stimulated by calcium. Our enzymatic assays of AtGDH1 established that its sensitivity to calcium is negligible. In vivo the AtGDH1-3 enzymes form homo- and heterohexamers of varied composition. We solved the crystal structure of recombinant AtGDH1 in the apo-form and in complex with NAD+ at 2.59 and 2.03 Å resolution, respectively. We demonstrate also that both in the apo form and in 1:1 complex with NAD+, it forms D3-symmetric homohexamers. A subunit of AtGDH1 consists of domain I, which is involved in hexamer formation and substrate binding, and of domain II which binds coenzyme. Most of the subunits in our crystal structures, including those in NAD+ complex, are in open conformation, with domain II forming a large (albeit variable) angle with domain I. One of the subunits of the AtGDH1-NAD+ hexamer contains a serendipitous 2OG molecule in the active site, causing a dramatic (∼25°) closure of the domains. We provide convincing evidence that the N-terminal peptide preceding domain I is a mitochondrial targeting signal, with a predicted cleavage site for mitochondrial processing peptidase (MPP) at Leu17-Leu18 that is followed by an unexpected potassium coordination site (Ser27, Ile30). We also identified several MPD [(+/-)-2-methyl-2,4-pentanediol] binding sites with conserved sequence. Although AtGDH1 is insensitive to MPD in our assays, the observation of druggable sites opens a potential for non-competitive herbicide design

    Heptabladed β‐propeller lectins PLL2 and PHL from Photorhabdus spp. recognize O ‐methylated sugars and influence the host immune system

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    O‐methylation is an unusual sugar modification with a function that is not fully understood. Given its occurrence and recognition by lectins involved in the immune response, methylated sugars were proposed to represent a conserved pathogen‐associated molecular pattern. We describe the interaction of O‐methylated saccharides with two β‐propeller lectins, the newly described PLL2 from the entomopathogenic bacterium Photorhabdus laumondii, and its homologue PHL from the related human pathogen Photorhabdus asymbiotica. The crystal structures of PLL2 and PHL revealed up to 10 out of 14 potential binding sites per protein subunit to be occupied with O‐methylated structures. The avidity effect strengthens the interaction by 4 orders of magnitude. PLL2 and PHL also interfere with the early immune response by modulating the production of reactive oxygen species and phenoloxidase activity. Since bacteria from Photorhabdus spp. have a complex life cycle involving pathogenicity towards different hosts, the involvement of PLL2 and PHL might contribute to the pathogen overcoming insect and human immune system defences in the early stages of infection

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