25 research outputs found

    Precise charged particle timing with the PICOSEC detector

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    The experimental requirements in near future accelerators (e.g. High Luminosity-LHC) has stimulated intense interestin development of detectors with high precision timing capabilities. With this as a goal, a new detection concept called PICOSEC,which is based to a “two-stage” MicroMegas detector coupled to a Cherenkov radiator equipped with a photocathode has beendeveloped. Results obtained with this new detector yield a time resolution of 24 ps for 150 GeV muons and 76 ps for single pho-toelectrons. In this paper we will report on the performance of the PICOSEC in test beams, as well as simulation studies andmodelling of its timing characteristicsPeer reviewe

    Imaging of Lipid Uptake in <i>Arabidopsis</i> Seedlings Utilizing Fluorescent Lipids and Confocal Microscopy

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    Eukaryotic cells use a diverse set of transporters to control the movement of lipids across their plasma membrane, which drastically affects membrane properties. Various tools and techniques to analyze the activity of these transporters have been developed. Among them, assays based on fluorescent phospholipid probes are particularly suitable, allowing for imaging and quantification of lipid internalization in living cells. Classically, these assays have been applied to yeast and animal cells. Here, we describe the adaptation of this powerful approach to characterize lipid internalization in plant roots and aerial tissues using confocal imaging. Graphic abstract: [Image: see text] Fluorescent lipid uptake in Arabidopsis seedlings. Scale bars: seedling, 25 mm; leaf, 10 μm; root, 25 μm

    Serum albumin promotes ATP-binding cassette transporter-dependent sterol uptake in yeast

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    Sterol uptake in fungi is a multistep process that involves interaction between external sterols and the cell wall, incorporation of sterol molecules into the plasma membrane, and subsequent integration into intracellular membranes for turnover. ATP-binding cassette (ABC) transporters have been implicated in sterol uptake, but key features of their activity remain to be elucidated. Here, we apply fluorescent cholesterol (NBD-cholesterol) to monitor sterol uptake under anaerobic and aerobic conditions in two fungal species, Candida glabrata (Cg) and Saccharomyces cerevisiae (Sc). We found that in both fungal species, ABC transporter-dependent uptake of cholesterol under anaerobic conditions and in mutants lacking HEM1 gene is promoted in the presence of the serum protein albumin that is able to bind the sterol molecule. Furthermore, the C. glabrata ABC transporter CgAus1p expressed in S. cerevisiae requires the presence of serum or albumin for efficient cholesterol uptake. These results suggest that albumin can serve as sterol donor in ABC transporter-dependent sterol uptake, a process potentially important for growth of C. glabrata inside infected humans

    Synthesis and Thermotropic Phase Behavior of Four Glycoglycerolipids

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    Four glycoglycerolipids with different head groups have been synthesized and their physicochemical properties studied. The lengths of the head groups from a mono-saccharide to a trisaccharide, in addition to the anomeric stereochemistry for the smaller glycoglycerolipids, have been modified. The synthesis has been optimized to avoid glycerol epimerization and to allow up-scaling. The physicochemical properties of the glycoglycerolipids were studied and a strong de-mixing of the gel-phase, depending on the head-group, was observed

    Synthesis and Thermotropic Phase Behavior of Four Glycoglycerolipids

    No full text
    Four glycoglycerolipids with different head groups have been synthesized and their physicochemical properties studied. The lengths of the head groups from a mono-saccharide to a trisaccharide, in addition to the anomeric stereochemistry for the smaller glycoglycerolipids, have been modified. The synthesis has been optimized to avoid glycerol epimerization and to allow up-scaling. The physicochemical properties of the glycoglycerolipids were studied and a strong de-mixing of the gel-phase, depending on the head-group, was observed
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