38 research outputs found

    Galactic winds and stellar populations in Lyman α\alpha emitting galaxies at z ~ 3.1

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    We present a sample of 33 spectroscopically confirmed z ~ 3.1 Lyα\alpha-emitting galaxies (LAEs) in the Cosmological Evolution Survey (COSMOS) field. This paper details the narrow-band survey we conducted to detect the LAE sample, the optical spectroscopy we performed to confirm the nature of these LAEs, and a new near-infrared spectroscopic detection of the [O III] 5007 \AA\ line in one of these LAEs. This detection is in addition to two [O III] detections in two z ~ 3.1 LAEs we have reported on previously (McLinden et al 2011). The bulk of the paper then presents detailed constraints on the physical characteristics of the entire LAE sample from spectral energy distribution (SED) fitting. These characteristics include mass, age, star-formation history, dust content, and metallicity. We also detail an approach to account for nebular emission lines in the SED fitting process - wherein our models predict the strength of the [O III] line in an LAE spectrum. We are able to study the success of this prediction because we can compare the model predictions to our actual near-infrared observations both in galaxies that have [O III] detections and those that yielded non-detections. We find a median stellar mass of 6.9 ×\times 108^8 M_{\odot} and a median star formation rate weighted stellar population age of 4.5 ×\times 106^6 yr. In addition to SED fitting, we quantify the velocity offset between the [O III] and Lyα\alpha lines in the galaxy with the new [O III] detection, finding that the Lyα\alpha line is shifted 52 km s1^{-1} redwards of the [O III] line, which defines the systemic velocity of the galaxy.Comment: 38 pages, 27 figures, 4 tables, Accepted for publication in MNRA

    The Dynamical Masses, Densities, and Star Formation Scaling Relations of Lyman Alpha Galaxies

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    We present the first dynamical mass measurements for Lyman alpha galaxies at high redshift, based on velocity dispersion measurements from rest-frame optical emission lines and size measurements from HST imaging, for a sample of nine galaxies drawn from four surveys. These measurements enable us to study the nature of Lyman alpha galaxies in the context of galaxy scaling relations. The resulting dynamical masses range from 1e9 to 1e10 solar masses. We also fit stellar population models to our sample, and use them to plot the Lyman alpha sample on a stellar mass vs. line width relation. Overall, the Lyman alpha galaxies follow well the scaling relation established by observing star forming galaxies at lower redshift (and without regard for Lyman alpha emission), though in 1/3 of the Lyman alpha galaxies, lower-mass fits are also acceptable. In all cases, the dynamical masses agree with established stellarmass-linewidth relation. Using the dynamical masses as an upper limit on gas mass, we show that Lyman alpha galaxies resemble starbursts (rather than "normal" galaxies) in the relation between gas mass surface density and star formation activity, in spite of relatively modest star formation rates. Finally, we examine the mass densities of these galaxies, and show that their future evolution likely requires dissipational ("wet") merging. In short, we find that Lyman alpha galaxies are low mass cousins of larger starbursts.Comment: Submitted to The Astrophysical Journal. 23 pp including three figures and four table

    Prediction of peptide and protein propensity for amyloid formation

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    Understanding which peptides and proteins have the potential to undergo amyloid formation and what driving forces are responsible for amyloid-like fiber formation and stabilization remains limited. This is mainly because proteins that can undergo structural changes, which lead to amyloid formation, are quite diverse and share no obvious sequence or structural homology, despite the structural similarity found in the fibrils. To address these issues, a novel approach based on recursive feature selection and feed-forward neural networks was undertaken to identify key features highly correlated with the self-assembly problem. This approach allowed the identification of seven physicochemical and biochemical properties of the amino acids highly associated with the self-assembly of peptides and proteins into amyloid-like fibrils (normalized frequency of β-sheet, normalized frequency of β-sheet from LG, weights for β-sheet at the window position of 1, isoelectric point, atom-based hydrophobic moment, helix termination parameter at position j+1 and ΔGº values for peptides extrapolated in 0 M urea). Moreover, these features enabled the development of a new predictor (available at http://cran.r-project.org/web/packages/appnn/index.html) capable of accurately and reliably predicting the amyloidogenic propensity from the polypeptide sequence alone with a prediction accuracy of 84.9 % against an external validation dataset of sequences with experimental in vitro, evidence of amyloid formation

    A novel a-L-Arabinofuranosidase of Family 43 Glycoside Hydrolase (Ct43Araf ) from Clostridium thermocellum

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    Articles in International JournalsThe study describes a comparative analysis of biochemical, structural and functional properties of two recombinant derivatives from Clostridium thermocellum ATCC 27405 belonging to family 43 glycoside hydrolase. The family 43 glycoside hydrolase encoding a-L-arabinofuranosidase (Ct43Araf) displayed an N-terminal catalytic module CtGH43 (903 bp) followed by two carbohydrate binding modules CtCBM6A (405 bp) and CtCBM6B (402 bp) towards the C-terminal. Ct43Araf and its truncated derivative CtGH43 were cloned in pET-vectors, expressed in Escherichia coli and functionally characterized. The recombinant proteins displayed molecular sizes of 63 kDa (Ct43Araf) and 34 kDa (CtGH43) on SDS-PAGE analysis. Ct43Araf and CtGH43 showed optimal enzyme activities at pH 5.7 and 5.4 and the optimal temperature for both was 50uC. Ct43Araf and CtGH43 showed maximum activity with rye arabinoxylan 4.7 Umg21 and 5.0 Umg21, respectively, which increased by more than 2-fold in presence of Ca2+ and Mg2+ salts. This indicated that the presence of CBMs (CtCBM6A and CtCBM6B) did not have any effect on the enzyme activity. The thin layer chromatography and high pressure anion exchange chromatography analysis of Ct43Araf hydrolysed arabinoxylans (rye and wheat) and oat spelt xylan confirmed the release of L-arabinose. This is the first report of a-L-arabinofuranosidase from C. thermocellum having the capacity to degrade both pnitrophenol- a-L-arabinofuranoside and p-nitrophenol-a-L-arabinopyranoside. The protein melting curves of Ct43Araf and CtGH43 demonstrated that CtGH43 and CBMs melt independently. The presence of Ca2+ ions imparted thermal stability to both the enzymes. The circular dichroism analysis of CtGH43 showed 48% b-sheets, 49% random coils but only 3% a-helices

    Dopamine neurons modulate neural encoding and expression of depression-related behaviour

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    Major depression is characterized by diverse debilitating symptoms that include hopelessness and anhedonia1. Dopamine neurons involved in reward and motivation are among many neural populations that have been hypothesized to be relevant, and certain antidepressant treatments, including medications and brain stimulation therapies, can influence the complex dopamine system. Until now it has not been possible to test this hypothesis directly, even in animal models, as existing therapeutic interventions are unable to specifically target dopamine neurons. Here we investigated directly the causal contributions of defined dopamine neurons to multidimensional depression-like phenotypes induced by chronic mild stress, by integrating behavioural, pharmacological, optogenetic and electrophysiological methods in freely moving rodents. We found that bidirectional control (inhibition or excitation) of specified midbrain dopamine neurons immediately and bidirectionally modulates (induces or relieves) multiple independent depression symptoms caused by chronic stress. By probing the circuit implementation of these effects, we observed that optogenetic recruitment of these dopamine neurons potently alters the neural encoding of depression-related behaviours in the downstream nucleus accumbens of freely moving rodents, suggesting that processes affecting depression symptoms may involve alterations in the neural encoding of action in limbic circuitry

    The Hobby–Eberly Telescope Dark Energy Experiment (HETDEX) Survey Design, Reductions, and Detections

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    We describe the survey design, calibration, commissioning, and emission-line detection algorithms for the Hobby–Eberly Telescope Dark Energy Experiment (HETDEX). The goal of HETDEX is to measure the redshifts of over a million Lyα emitting galaxies between 1.88 < z < 3.52, in a 540 deg2 area encompassing a comoving volume of 10.9 Gpc3. No preselection of targets is involved; instead the HETDEX measurements are accomplished via a spectroscopic survey using a suite of wide-field integral field units distributed over the focal plane of the telescope. This survey measures the Hubble expansion parameter and angular diameter distance, with a final expected accuracy of better than 1%. We detail the project’s observational strategy, reduction pipeline, source detection, and catalog generation, and present initial results for science verification in the Cosmological Evolution Survey, Extended Groth Strip, and Great Observatories Origins Deep Survey North fields. We demonstrate that our data reach the required specifications in throughput, astrometric accuracy, flux limit, and object detection, with the end products being a catalog of emission-line sources, their object classifications, and flux-calibrated spectra

    AI is a viable alternative to high throughput screening: a 318-target study

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    : High throughput screening (HTS) is routinely used to identify bioactive small molecules. This requires physical compounds, which limits coverage of accessible chemical space. Computational approaches combined with vast on-demand chemical libraries can access far greater chemical space, provided that the predictive accuracy is sufficient to identify useful molecules. Through the largest and most diverse virtual HTS campaign reported to date, comprising 318 individual projects, we demonstrate that our AtomNet® convolutional neural network successfully finds novel hits across every major therapeutic area and protein class. We address historical limitations of computational screening by demonstrating success for target proteins without known binders, high-quality X-ray crystal structures, or manual cherry-picking of compounds. We show that the molecules selected by the AtomNet® model are novel drug-like scaffolds rather than minor modifications to known bioactive compounds. Our empirical results suggest that computational methods can substantially replace HTS as the first step of small-molecule drug discovery
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