Design and performance of a vacuum-UV simulator for material testing under space conditions

This paper describes the construction and performance of a VUV-simulator that has been designed to study degradation of materials under space conditions. It is part of the Complex Irradiation Facility at DLR in Bremen, Germany, that has been built for testing of material under irradiation in the complete UV-range as well as under proton and electron irradiation. Presently available UV-sources used for material tests do not allow the irradiation with wavelengths smaller than about $115$ nm where common Deuterium lamps show an intensity cut-off. The VUV-simulator generates radiation by excitation of a gas-flow with an electron beam. The intensity of the radiation can be varied by manipulating the gas-flow and/or the electron beam. The VUV simulator has been calibrated at three different gas-flow settings in the range from $40$ nm to $410$ nm. The calibration has been made by the Physikalisch-Technische Bundesanstalt (PTB) in Berlin. The measured spectra show total irradiance intensities from $24$ to $58$ mW$\rm{m^{-2}}$ (see Table 4.2) in the VUV-range, i.e. for wavelengths smaller than $200$ nm. They exhibit a large number of spectral lines generated either by the gas-flow constituents or by metal atoms in the residual gas which come from metals used in the source construction. In the range from $40$ nm to $120$ nm where Deuterium lamps are not usable, acceleration factors of $3$ to $26.3$ Solar Constants are reached depending on the gas-flow setting. The VUV-simulator allows studies of general degradation effects caused by photoionization and photodissociation as well as accelerated degradation tests by use of intensities that are significantly higher compared to that of the Sun at $1$ AU

WLRS

This status-report of the Wettzell Laser Ranging System (WLRS) gives an overview of its set up and the developments necessary to make the system operational

Measuring atmospheric dispersion with WLRS in multiple wavelength mode

The WLRS (Wettzell Laser Ranging System) allows the simultaneous tracking of satellites on two different wavelengths. These are the fundamental frequency of Nd:YAG at 1.064 microns and the second harmonic at 532 nm. Range measurements to the satellite LAGEOS were carried out with different experimental set-ups, after developing a detector unit based on a silicon avalanche photodiode in Geiger mode, which is sufficiently sensitive in the infrared domain. An approach towards a quantitative interpretation of the data is suggested and discussed briefly

Reactive Oxygen Species Are Key Mediators of Demyelination in Canine Distemper Leukoencephalitis but not in Theiler’s Murine Encephalomyelitis

(1) Background: Canine distemper virus (CDV)-induced demyelinating leukoencephalitis (CDV-DL) in dogs and Theiler’s murine encephalomyelitis (TME) virus (TMEV)-induced demyelinating leukomyelitis (TMEV-DL) are virus-induced demyelinating conditions mimicking Multiple Sclerosis (MS). Reactive oxygen species (ROS) can induce the degradation of lipids and nucleic acids to characteristic metabolites such as oxidized lipids, malondialdehyde, and 8-hydroxyguanosine. The hypothesis of this study is that ROS are key eector molecules in the pathogenesis of myelin membrane breakdown in CDV-DL and TMEV-DL. (2) Methods: ROS metabolites and antioxidative enzymes were assessed using immunofluorescence in cerebellar lesions of naturally CDV-infected dogs and spinal cord tissue of TMEV-infected mice. The transcription of selected genes involved in ROS generation and detoxification was analyzed using gene-expression microarrays in CDV-DL and TMEV-DL. (3) Results: Immunofluorescence revealed increased amounts of oxidized lipids, malondialdehyde, and 8-hydroxyguanosine in CDV-DL while TMEV-infected mice did not reveal marked changes. In contrast, microarray-analysis showed an upregulated gene expression associated with ROS generation in both diseases. (4) Conclusion: In summary, the present study demonstrates a similar upregulation of gene-expression of ROS generation in CDV-DL and TMEV-DL. However, immunofluorescence revealed increased accumulation of ROS metabolites exclusively in CDV-DL. These results suggest dierences in the pathogenesis of demyelination in these two animal models

Autonomy and robustness of translocation through the nuclear pore complex: a single-molecule study

All molecular traffic between nucleus and cytoplasm occurs via the nuclear pore complex (NPC) within the nuclear envelope. In this study we analyzed the interactions of the nuclear transport receptors kapα2, kapβ1, kapβ1ΔN44, and kapβ2, and the model transport substrate, BSA-NLS, with NPCs to determine binding sites and kinetics using single-molecule microscopy in living cells. Recombinant transport receptors and BSA-NLS were fluorescently labeled by AlexaFluor 488, and microinjected into the cytoplasm of living HeLa cells expressing POM121-GFP as a nuclear pore marker. After bleaching the dominant GFP fluorescence the interactions of the microinjected molecules could be studied using video microscopy with a time resolution of 5 ms, achieving a colocalization precision of 30 nm. These measurements allowed defining the interaction sites with the NPCs with an unprecedented precision, and the comparison of the interaction kinetics with previous in vitro measurements revealed new insights into the translocation mechanism

The novel protein KBP regulates mitochondria localization by interaction with a kinesin-like protein

BACKGROUND: Members of the Kinesin-3 family of kinesin-like proteins mediate transport of axonal vesicles (KIF1A, KIF1Bβ), distribution of mitochondria (KIF1Bα) and anterograde Golgi to ER vesicle transport (KIF1C). Until now, little is known about the regulation of kinesin-like proteins. Several proteins interact with members of this protein family. Here we report on a novel, KIF1 binding protein (KBP) that was identified in yeast two-hybrid screens. RESULTS: KBP was identified by using the yeast-two-hybrid system with an amino-terminal fragment of KIF1C as a bait that is strongly homologous to KIF1B. Here we investigated the interaction of KBP and KIF1B. The full length proteins coimmunoprecipitated after overexpression and in untransfected 293 cells. Immunofluorescence experiments revealed that KBP was mainly localized to mitochondria, as has been described for KIF1Bα. Overexpression of a deletion mutant or reduction of the KBP protein level using an anti-sense construct led to an aggregation of mitochondria. Such an effect is probably due to the lower activity of KIF1Bα in the absence of KBP, as was revealed in motility assays. CONCLUSION: KBP is a new binding partner for KIF1Bα that is a regulator of its transport function and thus represents a new type of kinesin interacting protein

Ausência de bloqueio adrenérgico do ácido ortocarboxibenzeno selenínico, na galinha

The authors have demonstrated that ortho-carboxybenzeno seleninic acid 5 mg/Kg don’t reverse the effect of injected epinephrine, in the arterial pressure of the fowl, under uretane anesthesia.O artigo apresenta resumo em inglês

Using high‐resolution XRF analyses as a sequence stratigraphic tool in a mudstone‐dominated succession (Early Cretaceous, Lower Saxony Basin, Northern Germany)

Delineation of stratigraphic sequences and their component systems tracts in mudstone‐dominated successions is challenging due to the relatively homogenous, fine‐grained nature of the strata. High‐resolution elemental intensity data from X‐ray fluorescence core scanning is used in order to develop a sequence stratigraphic framework for the Lower Cretaceous monotonous mudstone succession in the eastern Lower Saxony Basin. The study is based on four drill cores covering the Berriasian to Aptian interval. In addition, carbon isotope (δ13Corg), grain size and CaCO3 analyses were carried out on discrete samples. The studied cores represent both proximal and distal basinal environments of the eastern Lower Saxony Basin and can be reliably correlated by utilizing variations in selected X‐ray flourescence elemental ratios, K/Ti data have proven to be particularly suitable in this regard. The core correlation shows that chemostratigraphic variability within the studied succession is laterally reproducible in the eastern Lower Saxony Basin, and can be used to establish a sequence stratigraphic framework. Further, Si/Al and Ca/Ti ratios have been applied to characterize the cores in terms of variation in grain size and CaCO3 content, respectively. Vertical grading trends inferred from Si/Al changes were used to identify transgressive and regressive systems tracts within the studied succession. An important regression in the uppermost lower Valanginian coincides with the onset of the Valanginian Weissert Event, as indicated by the well‐known positive δ13C shift, and, thus, supports the idea that the initial interval of this event corresponds to enhanced supply of terrigenous material. The results of this study are also in agreement with previously recognized transgressive–regressive trends in the Lower Saxony Basin and adjacent areas. This clearly shows that systematic geochemical variations recorded in mudstone‐dominated basinal settings are suitable to establish sequence stratigraphic frameworks

Nuclear transport of single molecules: dwell times at the nuclear pore complex

The mechanism by which macromolecules are selectively translocated through the nuclear pore complex (NPC) is still essentially unresolved. Single molecule methods can provide unique information on topographic properties and kinetic processes of asynchronous supramolecular assemblies with excellent spatial and time resolution. Here, single-molecule far-field fluorescence microscopy was applied to the NPC of permeabilized cells. The nucleoporin Nup358 could be localized at a distance of 70 nm from POM121-GFP along the NPC axis. Binding sites of NTF2, the transport receptor of RanGDP, were observed in cytoplasmic filaments and central framework, but not nucleoplasmic filaments of the NPC. The dwell times of NTF2 and transportin 1 at their NPC binding sites were 5.8 ± 0.2 and 7.1 ± 0.2 ms, respectively. Notably, the dwell times of these receptors were reduced upon binding to a specific transport substrate, suggesting that translocation is accelerated for loaded receptor molecules. Together with the known transport rates, our data suggest that nucleocytoplasmic transport occurs via multiple parallel pathways within single NPCs