Pressure dependence of the spin dynamics around a quantum critical point : An inelastic neutron scattering study of Ce0.87La0.13Ru2Si2

Inelastic neutron scattering experiments performed on a single crystal of the antiferromagnetic compound Ce$_{0.87}$La$_{0.13}$Ru$_{2}$Si$_{2}$ under applied pressures of up to 5 kbar are reported. A quantum critical point is reached at around 2.6 kbar where long-range magnetic order disappears. The variation of the characteristic energy scales with respect to temperature and pressure is followed and found to saturate in the ordered phase.Comment: 14 pages (6 figures

Internal lipid synthesis and vesicle growth as a step toward self-reproduction of the minimal cell

One of the major properties of the semi-synthetic minimal cell, as a model for early living cells, is the ability to self-reproduce itself, and the reproduction of the boundary layer or vesicle compartment is part of this process. A minimal bio-molecular mechanism based on the activity of one single enzyme, the FAS-B (Fatty Acid Synthase) Type I enzyme from Brevibacterium ammoniagenes, is encapsulated in 1-palmitoyl-2oleoyl-sn-glycero-3-phosphatidylcholine (POPC) liposomes to control lipid synthesis. Consequently molecules of palmitic acid released from the FAS catalysis, within the internal lumen, move toward the membrane compartment and become incorporated into the phospholipid bilayer. As a result the vesicle membranes change in lipid composition and liposome growth can be monitored. Here we report the first experiments showing vesicles growth by catalysis of one enzyme only that produces cell boundary from within. This is the prototype of the simplest autopoietic minimal cell

Relaxin-like factor (RLF)/insulin-like peptide 3 (INSL3) is secreted from testicular Leydig cells as a monomeric protein comprising three domains B–C–A with full biological activity in boars

RLF (relaxin-like factor), also known as INSL3 (insulin-like peptide 3), is a novel member of the relaxin/insulin gene family that is expressed in testicular Leydig cells. Despite the implicated role of RLF/INSL3 in testis development, its native conformation remains unknown. In the present paper we demonstrate for the first time that boar testicular RLF/INSL3 is isolated as a monomeric structure with full biological activity. Using a series of chromatography steps, the native RLF/INSL3 was highly purified as a single peak in reverse-phase HPLC. MS/MS (tandem MS) analysis of the trypsinized sample provided 66% sequence coverage and revealed a distinct monomeric structure consisting of the B-, C- and A-domains deduced previously from the RLF/INSL3 cDNA. Moreover, the N-terminal peptide was four amino acid residues longer than predicted previously. MS analysis of the intact molecule and PMF (peptide mass fingerprinting) analysis at 100% sequence coverage confirmed this structure and indicated the existence of three site-specific disulfide bonds. RLF/INSL3 retained full bioactivity in HEK (human embryonic kidney)-293 cells expressing RXFP2 (relaxin/insulin-like family peptide receptor 2), the receptor for RLF/INSL3. Furthermore, RLF/INSL3 was found to be secreted from Leydig cells into testicular venous blood. Collectively, these results indicate that boar RLF/INSL3 is secreted from testicular Leydig cells as a B–C–A monomeric structure with full biological activity

Germline Transgenic Pigs by Sleeping Beauty Transposition in Porcine Zygotes and Targeted Integration in the Pig Genome

Genetic engineering can expand the utility of pigs for modeling human diseases, and for developing advanced therapeutic approaches. However, the inefficient production of transgenic pigs represents a technological bottleneck. Here, we assessed the hyperactive Sleeping Beauty (SB100X) transposon system for enzyme-catalyzed transgene integration into the embryonic porcine genome. The components of the transposon vector system were microinjected as circular plasmids into the cytoplasm of porcine zygotes, resulting in high frequencies of transgenic fetuses and piglets. The transgenic animals showed normal development and persistent reporter gene expression for >12 months. Molecular hallmarks of transposition were confirmed by analysis of 25 genomic insertion sites. We demonstrate germ-line transmission, segregation of individual transposons, and continued, copy number-dependent transgene expression in F1-offspring. In addition, we demonstrate target-selected gene insertion into transposon-tagged genomic loci by Cre-loxP-based cassette exchange in somatic cells followed by nuclear transfer. Transposase-catalyzed transgenesis in a large mammalian species expands the arsenal of transgenic technologies for use in domestic animals and will facilitate the development of large animal models for human diseases

Characterization of dendritic growth in Fe-C system using time-resolved X-ray tomography and physics-based filtering

Joint 5th International Conference on Advances in Solidification Processes (ICASP-5) & 5th International Symposium on Cutting Edge of Computer Simulation of Solidification, Casting and Refining (CSSCR-5), 17–21 June 2019, Salzburg, AustriaTime-resolved in situ tomography of dendritic growth in Fe–0.45 mass% C carbon steel was performed using synchrotron radiation X-rays at SPring-8 synchrotron radiation facility (Japan) with improvement of the image quality using a physics-based filter. The voxel size of the reconstructed image was approximately 6.5 μm × 6.5 μm × 6.5 μm, and the time resolution (duration of 360° rotation) was 4 s (0.25 rps). Three-dimensional images of the dendrites were reconstructed even without image processing; however, the low contrast resolution in Fe–C alloys led to poor image quality. Consequently, it was impossible to precisely track the solid/liquid interface or evaluate the average curvature. To improve the image quality, a physics-based filter (a PF filter) was developed using a phase-field model. In the PF filter, images were retrieved in terms of interface curvature. The PF filter significantly improved the computed tomography image quality. As a result, dendritic growth was clearly observed even in Fe–C alloys. Moreover, the average curvature of the solid/liquid interface was evaluated as a function of solidification time (solid fraction). The ability to systematically characterize growing dendrites will be beneficial for modeling and simulation of solidification phenomena