Study of cryogenic fluid mixing techniques. Volume 1 - Large-scale experimental mixing investigations and liquid-oxygen mixer design Final report

Large-scale experimental liquid hydrogen mixing and liquid oxygen mixer desig

A study of cryogenic propellant mixing techniques. Volume 1 - Mixer design and experimental investigations Final report, Jul. 1967 - Sep. 1968

Mixer design and experimental tank study for cryogenic propellants, with applications for manned Mars missio

Discovery, isolation and structural characterization of cyclotides from Viola sumatrana miq

Cyclotides are cyclic peptides from plants in the Violaceae, Rubiaceae, Fabaceae, Cucurbitaceae, and Solanaceae families. They are sparsely distributed in most of these families, but appear to be ubiquitous in the Violaceae, having been found in every plant so far screened from this family. However, not all geographic regions have been examined and here we report the discovery of cyclotides from a Viola species from South-East Asia. Two novel cyclotides (Visu 1 and Visu 2) and two known cyclotides (kalata S and kalata B1) were identified in V. sumatrana. NMR studies revealed that kalata S and kalata B1 had similar secondary structures. Their biological activities were determined in cytotoxicity assays; both had similar cytotoxic activity and were more toxic to U87 cells compared with other cell lines. Overall, the study strongly supports the ubiquity of cyclotides in the Violaceae and adds to our understanding of their distribution and cytotoxic activity

A surprising method for polarising antiprotons

We propose a method for polarising antiprotons in a storage ring by means of a polarised positron beam moving parallel to the antiprotons. If the relative velocity is adjusted to $v/c \approx 0.002$ the cross section for spin-flip is as large as about $2 \cdot 10^{13}$ barn as shown by new QED-calculations of the triple spin-cross sections. Two possibilities for providing a positron source with sufficient flux density are presented. A polarised positron beam with a polarisation of 0.70 and a flux density of approximately $1.5 \cdot 10^{10}$/(mm$^2$ s) appears to be feasible by means of a radioactive $^{11}$C dc-source. A more involved proposal is the production of polarised positrons by pair production with circularly polarised photons. It yields a polarisation of 0.76 and requires the injection into a small storage ring. Such polariser sources can be used at low (100 MeV) as well as at high (1 GeV) energy storage rings providing a time of about one hour for polarisation build-up of about $10^{10}$ antiprotons to a polarisation of about 0.18. A comparison with other proposals show a gain in the figure-of-merit by a factor of about ten.Comment: 13 pages, 8 figures; v2: minor language and signification corrections v3: (14 pages, 12 figures) major error, nonapplicable polarisation transfer cross sections replaced by the mandatory spin-flip cross section

Heterogeneity of Nicotinic Receptor Class and Subunit mRNA Expression among Individual Parasympathetic Neurons from Rat Intracardiac Ganglia

Neurons have the potential to form thousands of distinct neuronal nicotinic receptors from the eight alpha and three beta subunits that currently are known. In an effort to determine how much of this potential complexity is realized among individual neurons, we examined the nicotinic pharmacological and biophysical properties and receptor subunit mRNA expression patterns in individual neurons cultured from rat epicardial ganglia. Analysis of the whole-cell pharmacology of these neurons showed a diversity of responses to the agonists acetylcholine, nicotine, cytisine, and 1,1-dimethyl-4-phenylpiperazinium, suggesting that a heterogeneous population of nicotinic receptor classes, or subtypes, is expressed by individual neurons. Single-channel analysis demonstrated three distinct conductances (18, 24, and 31 pS), with patches from different neurons containing different combinations of these channel classes. We used single-cell RT-PCR to examine nicotinic acetylcholine receptor (nAChR) subunit mRNA expression by individual neurons. Although mRNAs encoding all eight neuronal nAChR subunits for which we probed (alpha 2-alpha 5, alpha 7, beta 2-beta 4) were present in multicellular cultures, we found that individual epicardial neurons express distinct subsets of these nAChR subunit mRNAs. These results suggest that individual epicardial neurons express distinct arrays of nAChR subunits and that these subunits may assemble into functional receptors with distinct and variable subunit composition. This variable receptor subunit expression provides an explanation for the diversity of pharmacological and single-channel responses we have observed in individual neurons