103 research outputs found
Infra-patellar fat pad morphology and MRI signal distribution in advanced radiographic knee OA – Data from the OAI
Improved X-ray detection and particle identification with avalanche photodiodes
Avalanche photodiodes are commonly used as detectors for low energy x-rays.
In this work we report on a fitting technique used to account for different
detector responses resulting from photo absorption in the various APD layers.
The use of this technique results in an improvement of the energy resolution at
8.2 keV by up to a factor of 2, and corrects the timing information by up to 25
ns to account for space dependent electron drift time. In addition, this
waveform analysis is used for particle identification, e.g. to distinguish
between x-rays and MeV electrons in our experiment.Comment: 6 pages, 6 figure
The proton radius puzzle
High-precision measurements of the proton radius from laser spectroscopy of
muonic hydrogen demonstrated up to six standard deviations smaller values than
obtained from electron-proton scattering and hydrogen spectroscopy. The status
of this discrepancy, which is known as the proton radius puzzle will be
discussed in this paper, complemented with the new insights obtained from
spectroscopy of muonic deuterium.Comment: Moriond 2017 conference, 8 pages, 4 figure
Engineering the Controlled Assembly of Filamentous Injectisomes in E. coli K-12 for Protein Translocation into Mammalian Cells.
Bacterial pathogens containing type III protein secretion systems (T3SS) assemble large needle-like protein complexes in the bacterial envelope, called injectisomes, for translocation of protein effectors into host cells. The application of these molecular syringes for the injection of proteins into mammalian cells is hindered by their structural and genomic complexity, requiring multiple polypeptides encoded along with effectors in various transcriptional units (TUs) with intricate regulation. In this work, we have rationally designed the controlled expression of the filamentous injectisomes found in enteropathogenic Escherichia coli (EPEC) in the nonpathogenic strain E. coli K-12. All structural components of EPEC injectisomes, encoded in a genomic island called the locus of enterocyte effacement (LEE), were engineered in five TUs (eLEEs) excluding effectors, promoters and transcriptional regulators. These eLEEs were placed under the control of the IPTG-inducible promoter Ptac and integrated into specific chromosomal sites of E. coli K-12 using a marker-less strategy. The resulting strain, named synthetic injector E. coli (SIEC), assembles filamentous injectisomes similar to those in EPEC. SIEC injectisomes form pores in the host plasma membrane and are able to translocate T3-substrate proteins (e.g., translocated intimin receptor, Tir) into the cytoplasm of HeLa cells reproducing the phenotypes of intimate attachment and polymerization of actin-pedestals elicited by EPEC bacteria. Hence, SIEC strain allows the controlled expression of functional filamentous injectisomes for efficient translocation of proteins with T3S-signals into mammalian cells
Proton Structure from the Measurement of 2S-2P Transition Frequencies of Muonic Hydrogen
The Arabidopsis AtPNG1 gene encodes a peptide: N-glycanase
Deglycosylation of misfolded proteins by the endoplasmic reticulum-associated degradation (ERAD) pathway is catalyzed by peptide:N-glycanases (PNGases) that are highly conserved among mammals and yeast. The catalytic mechanism of PNGases employs a catalytic triad consisting of Cys, His and Asp residues, which is shared by other enzyme families such as cysteine proteases and protein cross-linking transglutaminases (TGases). In contrast to the yeast and mammalian systems, very little is known about ERAD in plants and the enzymes responsible for proper clearance of misfolded plant proteins. We have used a computer-based modeling approach to identify an Arabidopsis thaliana PNGase (AtPNG1). AtPNG1 is encoded by a single-copy gene and displays high structural homology with known PNGases. Importantly, heterologous expression of AtPNG1 restored N-glycanase activity in a PNGase-deficient Saccharomyces cerevisiae mutant. The AtPNG1 gene is uniformly and constitutively expressed at low levels throughout all developmental stages of the plant, and its expression does not appear to be subject to substantial regulation by external stimuli. Recently, recombinant AtPNG1 produced in Escherichia coli was reported to display TGase activity (Della Mea et al., Plant Physiol. 135, 2046-54, 2004). However, inactivation of the AtPNG1 gene did not result in decreased TGase activity in the mutant plant, and recombinant AtPNG1 produced in S. cerevisiae exhibited only residual TGase activity. We propose that the AtPNG1 gene encodes a bona fide peptide:N-glycanase that contributes to ERAD-related protein quality control in plants
Computergestützter Unternehmensablauf als Basis für die Allgemeine Betriebswirtschaftslehre
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