179 research outputs found

    X-ray luminescence computed tomography using a focused X-ray beam

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    Due to the low X-ray photon utilization efficiency and low measurement sensitivity of the electron multiplying charge coupled device (EMCCD) camera setup, the collimator based narrow beam X-ray luminescence computed tomography (XLCT) usually requires a long measurement time. In this paper, we, for the first time, report a focused X-ray beam based XLCT imaging system with measurements by a single optical fiber bundle and a photomultiplier tube (PMT). An X-ray tube with a polycapillary lens was used to generate a focused X-ray beam whose X-ray photon density is 1200 times larger than a collimated X-ray beam. An optical fiber bundle was employed to collect and deliver the emitted photons on the phantom surface to the PMT. The total measurement time was reduced to 12.5 minutes. For numerical simulations of both single and six fiber bundle cases, we were able to reconstruct six targets successfully. For the phantom experiment, two targets with an edge-to-edge distance of 0.4 mm and a center-to-center distance of 0.8 mm were successfully reconstructed by the measurement setup with a single fiber bundle and a PMT.Comment: 39 Pages, 12 Figures, 2 Tables, In submission (under review) to JB

    <i>Trypanosoma evansi</i>: Genetic variability detected using amplified restriction fragment length polymorphism (AFLP) and random amplified polymorphic DNA (RAPD) analysis of Kenyan isolates

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    We compared two methods to generate polymorphic markers to investigate the population genetics of Trypanosoma evansi; random amplified polymorphic DNA (RAPD) and amplified restriction fragment length polymorphism (AFLP) analyses. AFLP accessed many more polymorphisms than RAPD. Cluster analysis of the AFLP data showed that 12 T.evansi isolates were very similar (‘type A’) whereas 2 isolates differed substantially (‘type B’). Type A isolates have been generally regarded as genetically identical but AFLP analysis was able to identify multiple differences between them and split the type A T. evansi isolates into two distinct clades

    Imaging the Renner-Teller effect using laser-induced electron diffraction

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    Structural information on electronically excited neutral molecules can be indirectly retrieved, largely through pump-probe and rotational spectroscopy measurements with the aid of calculations. Here, we demonstrate the direct structural retrieval of neutral carbonyl disulfide (CS2_2) in the B1^1B2_2 excited electronic state using laser-induced electron diffraction (LIED). We unambiguously identify the ultrafast symmetric stretching and bending of the field-dressed neutral CS2_2 molecule with combined picometer and attosecond resolution using intrapulse pump-probe excitation and measurement. We invoke the Renner-Teller effect to populate the B1^1B2_2 excited state in neutral CS2_2, leading to bending and stretching of the molecule. Our results demonstrate the sensitivity of LIED in retrieving the geometric structure of CS2_2, which is known to appear as a two-center scatterer

    Calcium-Dependent Protein Kinases from Arabidopsis Show Substrate Specificity Differences in an Analysis of 103 Substrates

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    The identification of substrates represents a critical challenge for understanding any protein kinase-based signal transduction pathway. In Arabidopsis, there are more than 1000 different protein kinases, 34 of which belong to a family of Ca2+-dependent protein kinases (CPKs). While CPKs are implicated in regulating diverse aspects of plant biology, from ion transport to transcription, relatively little is known about isoform-specific differences in substrate specificity, or the number of phosphorylation targets. Here, in vitro kinase assays were used to compare phosphorylation targets of four CPKs from Arabidopsis (CPK1, 10, 16, and 34). Significant differences in substrate specificity for each kinase were revealed by assays using 103 different substrates. For example CPK16 phosphorylated Serine 109 in a peptide from the stress-regulated protein, Di19-2 with KM ∼70 μM, but this site was not phosphorylated significantly by CPKs 1, 10, or 34. In contrast, CPKs 1, 10, and 34 phosphorylated 93 other peptide substrates not recognized by CPK16. Examples of substrate specificity differences among all four CPKs were verified by kinetic analyses. To test the correlation between in vivo phosphorylation events and in vitro kinase activities, assays were performed with 274 synthetic peptides that contained phosphorylation sites previously mapped in proteins isolated from plants (in vivo-mapped sites). Of these, 74 (27%) were found to be phosphorylated by at least one of the four CPKs tested. This 27% success rate validates a robust strategy for linking the activities of specific kinases, such as CPKs, to the thousands of in planta phosphorylation sites that are being uncovered by emerging technologies

    Understanding and Visualizing Droplet Distributions in Simulations of Shallow Clouds

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    Thorough analysis of local droplet-level interactions is crucial to better understand the microphysical processes in clouds and their effect on the global climate. High-accuracy simulations of relevant droplet size distributions from Large Eddy Simulations (LES) of bin microphysics challenge current analysis techniques due to their high dimensionality involving three spatial dimensions, time, and a continuous range of droplet sizes. Utilizing the compact latent representations from Variational Autoencoders (VAEs), we produce novel and intuitive visualizations for the organization of droplet sizes and their evolution over time beyond what is possible with clustering techniques. This greatly improves interpretation and allows us to examine aerosol-cloud interactions by contrasting simulations with different aerosol concentrations. We find that the evolution of the droplet spectrum is similar across aerosol levels but occurs at different paces. This similarity suggests that precipitation initiation processes are alike despite variations in onset times.Comment: 4 pages, 3 figures, accepted at NeurIPS 2023 (Machine Learning and the Physical Sciences Workshop

    Isolation and Comparative Transcriptome Analysis of Human Fetal and iPSC-Derived Cone Photoreceptor Cells.

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    Loss of cone photoreceptors, crucial for daylight vision, has the greatest impact on sight in retinal degeneration. Transplantation of stem cell-derived L/M-opsin cones, which form 90% of the human cone population, could provide a feasible therapy to restore vision. However, transcriptomic similarities between fetal and stem cell-derived cones remain to be defined, in addition to development of cone cell purification strategies. Here, we report an analysis of the human L/M-opsin cone photoreceptor transcriptome using an AAV2/9.pR2.1:GFP reporter. This led to the identification of a cone-enriched gene signature, which we used to demonstrate similar gene expression between fetal and stem cell-derived cones. We then defined a cluster of differentiation marker combination that, when used for cell sorting, significantly enriches for cone photoreceptors from the fetal retina and stem cell-derived retinal organoids, respectively. These data may facilitate more efficient isolation of human stem cell-derived cones for use in clinical transplantation studies

    The fermion dynamical symmetry model for the even--even and even--odd nuclei in the Xe--Ba region

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    The even--even and even--odd nuclei 126^{126}Xe-132^{132}Xe and 131^{131}Ba-137^{137}Ba are shown to have a well-realized SO8SO6SO3SO_8 \supset SO_6 \supset SO_3 fermion dynamical symmetry. Their low-lying energy levels can be described by a unified analytical expression with two (three) adjustable parameters for even--odd (even--even) nuclei that is derived from the fermion dynamical symmetry model. Analytical expressions are given for wavefunctions and for E2E2 transition rates that agree well with data. The distinction between the FDSM and IBM SO6SO_6 limits is discussed. The experimentally observed suppression of the the energy levels with increasing SO5SO_5 quantum number τ\tau can be explained as a perturbation of the pairing interaction on the SO6SO_6 symmetry, which leads to an SO5SO_5 Pairing effect for SO6SO_6 nuclei.Comment: submitted to Phys. Rev. C, LaTeX, 31 pages, 8 figures with postscript files available on request at [email protected]
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