Present and future radioactive nuclear beam developments at Argonne

A scheme for building an ISOL-based radioactive nuclear beam facility at the Argonne Physics Division, is currently evaluated. The feasibility and efficiency of the different steps in the proposed production- and acceleration cycles are being tested. At the Dynamitron Facility of the ANL Physics Division, stripping yields of Kr, Xe and Ph beams in a windowless gas cell have been measured and the study of fission of {sup 238}U induced by fast neutrons from the {sup 9}Be(dn) reaction is in progress. Different aspects of the post-acceleration procedure are currently being investigated. In parallel with this work, energetic radioactive beams such as {sup 17}F, {sup 18}F and {sup 56}Ni have recently been developed at Argonne using the present ATLAS facility

Nuclear Reaction Studies with Radioactive {sup 18}F Beams at ATLAS

The contribution of the {sup 18}F(p,{gamma}) reaction to the production of {sup 19}Ne which is the crucial isotope for the breakout from the hot CNO cycle into the rp process, has been investigated in experiments with {sup 18}F beams. Measurements of the cross sections for the {sup 18}F(p,{alpha}){sup 15}O and the {sup 18}F(p,{gamma}){sup 19}Ne reactions indicate that the contribution from the (p,{gamma}) route to the formation of {sup 19}Ne is small

The Influence of {sup 18} F Induced Reactions in the Hot CNO Cycle

The contribution of the {sup 18}F(p,{gamma}) reaction to the production of {sup 19}Ne, which is an important isotope in connection with the breakout from the hot CNO cycle, has been investigated in experiments with {sup 18}F beams. Measurements of the cross sections for the {sup 18}F(p,{alpha}){sup 15}O and {sup 18}F(p,{gamma}){sup 19 }Ne reactions indicate that the contribution of the {sup 18}F(p, {gamma}) route to the formation or {sup 19}Ne is small

Low-Energy Direct Capture in the 8Li(n,gamma)9Li and 8B(p,gamma)9C Reactions

The cross sections of the 8Li(n,gamma)9Li and 8B(p,gamma)9C capture reactions have been analyzed using the direct capture model. At low energies which is the astrophysically relevant region the capture process is dominated by E1 transitions from incoming s-waves to bound p-states. The cross sections of both mirror reactions can be described simultaneously with consistent potential parameters, whereas previous calculations have overestimated the capture cross sections significantly. However, the parameters of the potential have to be chosen very carefully because the calculated cross section of the 8Li(n,gamma)9Li reaction depends sensitively on the potential strength.Comment: 6 pages, 5 figures, Phys. Rev. C, accepte

Selective regulation of IP3-receptor-mediated Ca2+ signaling and apoptosis by the BH4 domain of Bcl-2 versus Bcl-Xl

Antiapoptotic B-cell lymphoma 2 (Bcl-2) targets the inositol 1,4,5-trisphosphate receptor (IP3R) via its BH4 domain, thereby suppressing IP3R Ca2+-flux properties and protecting against Ca2+-dependent apoptosis. Here, we directly compared IP3R inhibition by BH4-Bcl-2 and BH4-Bcl-Xl. In contrast to BH4-Bcl-2, BH4-Bcl-Xl neither bound the modulatory domain of IP3R nor inhibited IP3-induced Ca2+ release (IICR) in permeabilized and intact cells. We identified a critical residue in BH4-Bcl-2 (Lys17) not conserved in BH4-Bcl-Xl (Asp11). Changing Lys17 into Asp in BH4-Bcl-2 completely abolished its IP3R-binding and -inhibitory properties, whereas changing Asp11 into Lys in BH4-Bcl-Xl induced IP3R binding and inhibition. This difference in IP3R regulation between BH4-Bcl-2 and BH4-Bcl-Xl controls their antiapoptotic action. Although both BH4-Bcl-2 and BH4-Bcl-Xl had antiapoptotic activity, BH4-Bcl-2 was more potent than BH4-Bcl-Xl. The effect of BH4-Bcl-2, but not of BH4-Bcl-Xl, depended on its binding to IP(3)Rs. In agreement with the IP3R-binding properties, the antiapoptotic activity of BH4-Bcl-2 and BH4-Bcl-Xl was modulated by the Lys/Asp substitutions. Changing Lys17 into Asp in full-length Bcl-2 significantly decreased its binding to the IP3R, its ability to inhibit IICR and its protection against apoptotic stimuli. A single amino-acid difference between BH4-Bcl-2 and BH4-Bcl-Xl therefore underlies differential regulation of IP(3)Rs and Ca2+-driven apoptosis by these functional domains. Mutating this residue affects the function of Bcl-2 in Ca2+ signaling and apoptosis

Evidence for bystander signalling between human trophoblast cells and human embryonic stem cells

Maternal exposure during pregnancy to toxins can occasionally lead to miscarriage and malformation. It is currently thought that toxins pass through the placental barrier, albeit bilayered in the first trimester, and damage the fetus directly, albeit at low concentration. Here we examined the responses of human embryonic stem (hES) cells in tissue culture to two metals at low concentration. We compared direct exposures with indirect exposures across a bi-layered model of the placenta cell barrier. Direct exposure caused increased DNA damage without apoptosis or a loss of cell number but with some evidence of altered differentiation. Indirect exposure caused increased DNA damage and apoptosis but without loss of pluripotency. This was not caused by metal ions passing through the barrier. Instead the hES cells responded to signalling molecules (including TNF-α) secreted by the barrier cells. This mechanism was dependent on connexin 43 mediated intercellular ‘bystander signalling’ both within and between the trophoblast barrier and the hES colonies. These results highlight key differences between direct and indirect exposure of hES cells across a trophoblast barrier to metal toxins. It offers a theoretical possibility that an indirectly mediated toxicity of hES cells might have biological relevance to fetal development

Spectroscopy of 193,195,197Po

Excited states built on the 13/21 isomers of the odd-mass 193,195,197Po isotopes have been observed via in-beam g-ray spectroscopy. The a radioactivity of these isotopes has been used to tag g -ray transitions following the AEr1164 MeV 32S reactions, where A5164, 166, 167, 168, and 170. Prompt g radiation was measured by ten Compton-suppressed Ge detectors at the target position and the Fragment Mass Analyzer was used to select evaporation residues. The results are compared with the first excited states of the heavier odd-mass polonium isotopes and of the even-mass cores

Multidimensional Atomic Force Microscopy: A Versatile Novel Technology for Nanopharmacology Research

Nanotechnology is giving us a glimpse into a nascent field of nanopharmacology that deals with pharmacological phenomena at molecular scale. This review presents our perspective on the use of scanning probe microscopy techniques with special emphasis to multidimensional atomic force microscopy (m-AFM) to explore this new field with a particular emphasis to define targets, design therapeutics, and track outcomes of molecular-scale pharmacological interactions. The approach will be to first discuss operating principles of m-AFM and provide representative examples of studies to understand human health and disease at the molecular level and then to address different strategies in defining target macromolecules, screening potential drug candidates, developing and characterizing of drug delivery systems, and monitoring target–drug interactions. Finally, we will discuss some future directions including AFM tip-based parallel sensors integrated with other high-throughput technologies which could be a powerful platform for drug discovery

Study of the 56Ni(d, p)57 Reaction and the Astrophysical 56Ni(p, γ)57Cu Reaction Rate

The single-particle character of states outside the doubly magic (radioactive) nucleus 56Ni has been determined through a measurement of the (d, p) neutron transfer reaction using inverse kinematics. From the spectroscopic factors of the low-lying states in 57Ni, the astrophysically interesting yield for the 56Ni(p, γ) reaction to the mirror nucleus 57Cu has been calculated, utilizing charge symmetry. The rate for this reaction in the temperature range typical of novae, supernovae, and x-ray bursts is found to be more than 10 times higher than previously assumed