Ambitious STS-7 mission to feature first landing at Kennedy

The STS-7 press briefing schedule, NASA select television schedule; launch preparations, countdown and liftoff; major countdown milestones; launch window; STS-7 flight sequence of events, landing timeline; STS-7 flight timeline; landing and post landing operations; flight objectives; Telesat's ANIK-C 2; PALAPA-B; STS-7 experiments; and spacecraft tracking and data network are presented

Jupiter's radiation belts: Can Pioneer 10 survive?

Model calculations of Jupiter's electron and proton radiation belts indicate that the Galilean satellites can reduce particle fluxes in certain regions of the inner magnetosphere by as much as six orders of magnitude. Average fluxes should be reduced by a factor of 100 or more along the Pioneer 10 trajectory through the heart of Jupiter's radiation belts in early December. This may be enough to prevent serious radiation damage to the spacecraft

Absorption of trapped particles by Jupiter's moons

Absorption effects of the four innermost moons in the radial transport equations for electrons and protons in Jupiter's magnetosphere are presented. The phase space density n at 2 R sub J for electrons with equatorial pitch angles less than 69 deg is reduced by a factor of 4.2 x 1000 when lunar absorption is included in the calculation. For protons with equatorial pitch angles less than 69 deg, the corresponding reduction factor is 3.2 x 100000. The effect of the satellites becomes progressively weaker for both electrons and protons as equatorial pitch angles of pi/2 are approached, because the likelihood of impacting a satellite becomes progressively smaller. The large density decreases which we find at the orbits of Io, Europa, and Ganymede result in corresponding particle flux decreases that should be observed by spacecraft making particle measurements in Jupiter's magnetosphere. The characteristic signature of satellite absorption should be a downward pointing cusp in the flux versus radius curve at the L-value corresponding to each satellite

Hidden assumptions in the derivation of the Theorem of Bell

John Bell's inequalities have already been considered by Boole in 1862. Boole established a one-to-one correspondence between experimental outcomes and mathematical abstractions of his probability theory. His abstractions are two-valued functions that permit the logical operations AND, OR and NOT and are the elements of an algebra. Violation of the inequalities indicated to Boole an inconsistency of definition of the abstractions and/or the necessity to revise the algebra. It is demonstrated in this paper, that a violation of Bell's inequality by Einstein-Podolsky-Rosen type of experiments can be explained by Boole's ideas. Violations of Bell's inequality also call for a revision of the mathematical abstractions and corresponding algebra. It will be shown that this particular view of Bell's inequalities points toward an incompleteness of quantum mechanics, rather than to any superluminal propagation or influences at a distance

What communities have to say: using focus groups for SVP planning.

Presented at: 2015 National Sexual Assault Conference; September 2-4, 2015; Los Angeles, CA.https://digitalrepository.unm.edu/prc-posters-presentations/1038/thumbnail.jp

Preventing sexual violence in New Mexico: what our communities have to say.

Presented at: 2015 Annual Conference of the New Mexico Public Health Association; March 31-April 1, 2015; Albuquerque, NM.https://digitalrepository.unm.edu/prc-posters-presentations/1036/thumbnail.jp

The steady-state repertoire of human SCF Ubiquitin ligase complexes does not require ongoing Nedd8 conjugation

The human genome encodes 69 different F-box proteins (FBPs), each of which can potentially assemble with Skp1-Cul1-RING to serve as the substrate specificity subunit of an SCF ubiquitin ligase complex. SCF activity is switched on by conjugation of the ubiquitin- like protein Nedd8 to Cul1. Cycles of Nedd8 conjugation and deconjugation acting in conjunction with the Cul1-sequestering factor Cand1 are thought to control dynamic cycles of SCF assembly and disassembly, which would enable a dynamic equilibrium between the Cul1- RING catalytic core of SCF and the cellular repertoire of FBPs. To test this hypothesis, we determined the cellular composition of SCF complexes and evaluated the impact of Nedd8 conjugation on this steady-state. At least 42 FBPs assembled with Cul1 in HEK 293 cells, and the levels of Cul1-bound FBPs varied by over two orders of magnitude. Unexpectedly, quantitative mass spectrometry revealed that blockade of Nedd8 conjugation led to a modest increase, rather than a decrease, in the overall level of most SCF complexes. We suggest that multiple mechanisms including FBP dissociation and turnover cooperate to maintain the cellular pool of SCF ubiquitin ligases

X-ray absorption spectroscopy on layered cobaltates Na_xCoO_2

Measurements of polarization and temperature dependent soft x-ray absorption have been performed on Na_xCoO_2 single crystals with x=0.4 and x=0.6. They show a deviation of the local trigonal symmetry of the CoO_6 octahedra, which is temperature independent in a temperature range between 25 K and 372 K. This deviation was found to be different for Co^{3+} and Co^{4+} sites. With the help of a cluster calculation we are able to interpret the Co L_{23}-edge absorption spectrum and find a doping dependent energy splitting between the t_{2g} and the e_g levels (10Dq) in Na_xCoO_2.Comment: 7 pages, 8 figure

O-linked glycosylation sites profiling in Mycobacterium tuberculosis culture filtrate proteins

Mycobacterium tuberculosis (Mtb) causes tuberculosis, one of the leading causes of fatal infectious diseases worldwide. Cell–cell recognition between the pathogen Mtb and its host is mediated in part by glycosylated proteins. So far, glycoproteins in Mtb are understudied and for only very few glycoproteins glycosylation sites have been described, e.g., alanine and proline rich secreted protein apa, superoxide dismutase SODC, lipoprotein lpqH and MPB83/MPT83. In this study, glycosylated proteins in Mtb culture filtrate were investigated using liquid chromatography–mass spectrometry approaches and bioinformatic analyses. To validate the presence of glycoproteins, several strategies were pursued including collision induced dissociation, high energy collision dissociation and electron transfer dissociation techniques, and bioinformatics analyses involving a neutral loss search for glycosylated moieties. After extensive data curation, we report glycosylation sites for thirteen Mtb glycoproteins using a combination of mass spectrometry techniques on a dataset collected from culture filtrate proteins. This is the first glycoproteomics study identifying glycosylation sites on mycobacterial culture filtrate proteins (CFP) on a global scale. Biological significance In this study, glycosylation sites in Mtb were characterized by collision-induced dissociation, electron-transfer dissociation and high energy collision dissociation techniques. The identification of glycosylation sites is important for our understanding of the physiology and pathophysiology of Mtb. Glycoproteins are often responsible for protein–protein interactions between host and pathogen and thus represent interesting targets for vaccine development. In addition, our strategy is not limited to Mtb, but could be extended to other organisms