1,830 research outputs found

    An updated stellar census of the Quintuplet cluster

    Get PDF
    Context. Found within the central molecular zone, the Quintuplet is one of the most massive young clusters in the Galaxy. As a consequence it offers the prospect of constraining stellar formation and evolution in extreme environments. However, current observations suggest that it comprises a remarkably diverse stellar population that is difficult to reconcile with an instantaneous formation event. Aims. To better understand the nature of the cluster our aim is to improve observational constraints on the constituent stars. Methods. In order to accomplish this goal we present Hubble Space Telescope/NICMOS+WFC3 photometry and Very Large Telescope/SINFONI+KMOS spectroscopy for ∼100 and 71 cluster members, respectively. Results. Spectroscopy of the cluster members reveals the Quintuplet to be far more homogeneous than previously expected. All supergiants are classified as either O7–8 Ia or O9–B0 Ia, with only one object of earlier (O5 I–III) spectral type. These stars form a smooth morphological sequence with a cohort of seven early-B hypergiants and six luminous blue variables and WN9-11h stars, which comprise the richest population of such stars of any stellar aggregate known. In parallel, we identify a smaller population of late-O hypergiants and spectroscopically similar WN8–9ha stars. No further H-free Wolf–Rayet (WR) stars are identified, leaving an unexpectedly extreme ratio of 13:1 for WC/WN stars. A subset of the O9–B0 supergiants are unexpectedly faint, suggesting they are both less massive and older than the greater cluster population. Finally, no main sequence objects were identifiable. Conclusions. Due to uncertainties over which extinction law to apply, it was not possible to quantitatively determine a cluster age via isochrone fitting. Nevertheless, we find an impressive coincidence between the properties of cluster members preceding the H-free WR phase and the evolutionary predictions for a single, non-rotating 60 M⊙ star; in turn this implies an age of ∼3.0–3.6 Myr for the Quintuplet. Neither the late O-hypergiants nor the low luminosity supergiants are predicted by such a path; we suggest that the former either result from rapid rotators or are the products of binary driven mass-stripping, while the latter may be interlopers. The H-free WRs must evolve from stars with an initial mass in excess of 60 M⊙ but it appears difficult to reconcile their observational properties with theoretical expectations. This is important since one would expect the most massive stars within the Quintuplet to be undergoing core-collapse/SNe at this time; since the WRs represent an evolutionary phase directly preceding this event,their physical properties are crucial to understanding both this process and the nature of the resultant relativistic remnant. As such, the Quintuplet provides unique observational constraints on the evolution and death of the most massive stars forming in the local, high metallicity Universe

    The Arches cluster revisited: II. A massive eclipsing spectroscopic binary in the Arches cluster

    Get PDF
    We have carried out a spectroscopic variability survey of some of the most massive stars in the Arches cluster, using K-band observations obtained with SINFONI on the VLT. One target, F2, exhibits substantial changes in radial velocity; in combination with new KMOS and archival SINFONI spectra, its primary component is found to undergo radial velocity variation with a period of 10.483+/-0.002 d and an amplitude of ~350 km/s-1. A secondary radial velocity curve is also marginally detectable. We reanalyse archival NAOS-CONICA photometric survey data in combination with our radial velocity results to confirm this object as an eclipsing SB2 system, and the first binary identified in the Arches. We model it as consisting of an 82+/-12 M⊙ WN8-9h primary and a 60+/-8 M⊙ O5-6 Ia+ secondary, and as having a slightly eccentric orbit, implying an evolutionary stage prior to strong binary interaction. As one of four X-ray bright Arches sources previously proposed as colliding-wind massive binaries, it may be only the first of several binaries to be discovered in this cluster, presenting potential challenges to recent models for the Arches' age and composition. It also appears to be one of the most massive binaries detected to date; the primary's calculated initial mass of >~120 M⊙ would arguably make this the most massive binary known in the Galaxy

    Decision and function problems based on boson sampling

    Get PDF
    Boson sampling is a mathematical problem that is strongly believed to be intractable for classical computers, whereas passive linear interferometers can produce samples efficiently. So far, the problem remains a computational curiosity, and the possible usefulness of boson-sampling devices is mainly limited to the proof of quantum supremacy. The purpose of this work is to investigate whether boson sampling can be used as a resource of decision and function problems that are computationally hard, and may thus have cryptographic applications. After the definition of a rather general theoretical framework for the design of such problems, we discuss their solution by means of a brute-force numerical approach, as well as by means of non-boson samplers. Moreover, we estimate the sample sizes required for their solution by passive linear interferometers, and it is shown that they are independent of the size of the Hilbert space.Comment: Close to the version published in PR

    Electron photodetachment from a Dirac bubble potential. A model for the fullerene negative ion C-60

    Full text link
    A model for the fullerene anion C-60 is proposed in which the outer electron moves in an attractive deltafunction potential in the shape of a spherical bubble. Exact solutions from this "Dirac bubble potential" were previously worked out. On the basis of this model, the photodetachment cross-section and its angular distribution are computed as functions of photoelectron energy, for the electron in both S-like and P-like bound states. Secondary maxima and minima in the cross section appear at higher energy values, somewhat analogous to the scattering of radiation from a conducting sphere.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/29792/1/0000134.pd

    Peptide microarray-based characterization of antibody responses to host proteins after bacille Calmette-Guerin vaccination

    Get PDF
    BACKGROUND: Bacille Calmette–Guérin (BCG) is the world’s most widely distributed vaccine, used against tuberculosis (TB), in cancer immunotherapy, and in autoimmune diseases due to its immunomodulatory properties. To date, the effect of BCG vaccination on antibody responses to host proteins has not been reported. High-content peptide microarrays (HCPM) offer a unique opportunity to gauge specific humoral immune responses. METHODS: The sera of BCG-vaccinated healthy adults were tested on a human HCPM platform (4953 randomly selected epitopes of human proteins) to detect specific immunoglobulin gamma (IgG) responses. Samples were obtained at 56, 112, and 252 days after vaccination. Immunohistology was performed on lymph node tissue from patients with TB lymphadenitis. Results were analysed with a combination of existing and novel statistical methods. RESULTS: IgG recognition of host peptides exhibited a peak at day 56 post BCG vaccination in all study subjects tested, which diminished over time. Primarily, IgG responses exhibited increased reactivity to ion transporters (sodium, calcium channels), cytokine receptors (interleukin 2 receptor β (IL2Rβ), fibroblast growth factor receptor 1 (FGFR1)), other cell surface receptors (inositol, somatostatin, angiopoeitin), ribonucleoprotein, and enzymes (tyrosine kinases, phospholipase) on day 56. There was decreased IgG reactivity to transforming growth factor-beta type 1 receptor (TGFβR1) and, in agreement with the peptide microarray findings, immunohistochemical analysis of TB-infected lymph node samples revealed an overexpression of TGFβR in granulomatous lesions. Moreover, the vesicular monoamine transporter (VMAT2) showed increased reactivity on days 112 and 252, but not on day 56 post-vaccination. IgG to interleukin 4 receptor (IL4R) showed increased reactivity at 112 days post-vaccination, while IgG to IL2Rβ and FGFR1 showed decreased reactivity on days 112 and 252 as compared to day 56 post BCG vaccination. CONCLUSIONS: BCG vaccination modifies the host’s immune landscape after 56 days, but this imprint changes over time. This may influence the establishment of immunological memory in BCG-vaccinated individuals

    Discovery of a potent deubiquitinase (DUB) small molecule activity‐based probe enables broad spectrum DUB activity profiling in living cells

    Get PDF
    Deubiquitinases (DUBs) are a family of >100 proteases that hydrolyze isopeptide bonds linking ubiquitin to protein substrates. This leads to reduced substrate degradation through the ubiquitin proteasome system. Deregulation of DUB activity has been implicated in many diseases, including cancer, neurodegeneration and auto-inflammation, and several have been recognized as attractive targets for therapeutic intervention. Ubiquitin-derived covalent activity-based probes (ABPs) provide a powerful tool for DUB activity profiling, but their large recognition element impedes cellular permeability and presents an unmet need for small molecule ABPs which can account for regulation of DUB activity in intact cells or organisms. Here, through comprehensive chemoproteomic warhead profiling, we identify cyanopyrrolidine (CNPy) probe IMP-2373 (12) as a small molecule pan-DUB ABP to monitor DUB activity in physiologically relevant live cells. Through proteomics and targeted assays, we demonstrate that IMP-2373 quantitatively engages more than 35 DUBs across a range of non-toxic concentrations in diverse cell lines. We further demonstrate its application to quantification of changes in intracellular DUB activity during pharmacological inhibition and during MYC deregulation in a model of B cell lymphoma. IMP-2373 thus offers a complementary tool to ubiquitin ABPs to monitor dynamic DUB activity in the context of disease-relevant phenotypes
    corecore