Theoretical analysis of direct CPCP violation and differential decay width in D±→π±π+π−D^\pm\to \pi^\pm \pi^+\pi^- in phase space around the resonances ρ0(770)\rho^0(770) and f0(500)f_0(500)

We perform a theoretical study on direct $CP$ violation in $D^\pm\to \pi^\pm \pi^+\pi^-$ in phase space around the intermediate states $\rho^0(770)$ and $f_0(500)$. The possible interference between the amplitudes corresponding to the two resonances is taken into account, and the relative strong phase of the two amplitudes is treated as a free parameter. Our analysis shows that by properly chosen the strong phase, both the $CP$ violation strength and differential decay width accommodate to the experimental results.Comment: 15 pages, 5 figure

An unprecedented binodal (4,6)-connected Co(II) MOF as dual-responsive luminescent sensor for detection of acetylacetone and Hg2+ ions

A new Co(II) organic framework, {[Co2(L)(hfpd)(H2O)]·1.75H2O}n (1) (H4hfpd = 4,4′-(hexafluoroisopropylidene)diphthalic acid, L = 4,4′-bis(imidazol-1-yl)-biphenyl) was hydrothermally synthesized and characterized. 1 possesses an unusual (4,6)-connected layered network architecture. Fluorescence titration results present that 1 is rarely dual-responsive probe to detect acetylacetone and Hg2+ ions by luminescence quenching.publishe

Lifshitz transitions in a heavy-Fermion liquid driven by short-range antiferromagnetic correlations in the two-dimensional Kondo lattice model

The heavy-Fermion liquid with short-range antiferromagnetic correlations is carefully considered in the two-dimensional Kondo-Heisenberg lattice model. As the ratio of the local Heisenberg superexchange $J_{H}$ to the Kondo coupling $J_{K}$ increases, Lifshitz transitions are anticipated, where the topology of the Fermi surface (FS) of the heavy quasiparticles changes from a hole-like circle to four kidney-like pockets centered around $(\pi ,\pi)$. In-between these two limiting cases, a first-order quantum phase transition is identified at $J_{H}/J_{K}=0.1055$ where a small circle begins to emerge within the large deformed circle. When $J_{H}/J_{K}=0.1425$, the two deformed circles intersect each other and then decompose into four kidney-like Fermi pockets via a second-order quantum phase transition. As $J_{H}/J_{K}$ increases further, the Fermi pockets are shifted along the direction ($\pi,\pi$) to ($\pi/2,\pi/2$), and the resulting FS is consistent with the FS obtained recently using the quantum Monte Carlo cluster approach to the Kondo lattice system in the presence of the antiferrmagnetic order.Comment: 4 pages, 5 figure

An endoglucanase, GsCelA, from Geobacilus sp. undergoes an intriguing self- truncation process for enhancing activity and thermostability

An endoglucanase, GsCelA, was isolated and cloned from a thermophilic Geobacillus sp. 70PC53 grown in a rice straw compost in southern Taiwan. It was observed that highly purified GsCelA was able to self-truncate, removing a segment of 53 amino acid residues from its C-terminus. The purified GsCelA does not possess any protease activity and this self-truncation process is insensitive to standard protease inhibitors except EDTA and EGTA. This unique self-truncation process takes place at a temperature higher than 10C with an optimal pH between 6-7, and can be further enhanced with certain divalent ions such as Ca+2 and Mg+2. Crystal structure of GsCelA has a typical TIM-barrel configuration with 8 alpha-helices and 8 beta-strands, but with the presence of a divalent ion. Mutations of amino acids residues surrounding this metal ion do not affect the self-truncation process, but some of these mutants have enhanced enzymatic activities. Mutation of the cleavage site between K315 and G316 does not affect the self-truncation process. However, a deletion of ten amino acids near the cleavage site, i.e. from amino acid 310 to 320, slows down the truncation process but does not block it, and a truncated form around 315 amino acids in length eventually appears. This intriguing observation indicates that the self-truncation process is not site specific, but capable of measuring 315 amino acids from the N-terminus as the cleavage site. This self-truncation process also occurs in the native host of this enzyme, Geobacillus sp. 70PC53, with almost all secreted form of this enzyme being self-truncated. The 53 amino-acid-long C-terminal segment removed by this self-truncation process has binding affinity toward both crystal and amorphous cellulose as well as the s cell walls, yet its sequence bears no apparent homology to any known carbohydrate binding motifs. Various other mutation analyses and the structure-based recombination process, SCHEMA, have been carried out, and both the activity and thermostabilty of this enzyme are further improved. The truncated and improved GsCelA has almost twice the activity as the un-truncated form, and its thermostability is also further enhanced with T50 reaching 86C and TA50 higher than 100C, making this enzyme extremely useful in industrial processes carried out at high temperatures, such as the pre-treatment of cellulosic animal feeds during the final drying step. This research was supported by grants from Taiwan Ministry of Science and Technology and from Academia Sinica

The Detection and Phylogenetic Analysis of Bovine Hepacivirus in China

Hepacivirus has been identified in cattle in Africa, Europe, and South America. In this survey of bovine hepacivirus (BovHepV) in 131 serum samples from Chinese cattle herds using RT-PCR, five of 131 sera were BovHepV positive, with the infection rate of 3.82%. Phylogenetic analysis based on the partial NS3 coding sequence showed that the BovHepV of the five positive samples clustered with other BovHepV but formed a separate branch. The results indicated that these new BovHepV represent emerging and novel strains. Further investigations are necessary to determine the epidemiology and viral pathogenesis of these BovHepV strains, as well as the potential threat to ruminant and livestock workers in China

Maintaining CD4/CD8 ratio and Th1-CTL subsets of chimeric antigen receptor (CAR)-T cells in serum-free culture conditions

Chimeric antigen receptor (CAR) T cells therapy is a promising strategy that significantly controlled the progress of cancer diseases. CAR-T cells could kill cancer cells through cellular immune response; therefore, CD8+ cytotoxic T cells are critical for CAR-T cell therapy. However, recent papers reported that CD4+ T helper cells were important for the response and maintenance of CAR-T cells in vivo. Here, we developed a serum-free CAR-T cell preparation process that maintained the T cell population and controlled the T cell subsets. The CD4+ and CD8+ T cell population in CAR-T cells were maintained at averagely 59.4 % and 34.6%, and the major T cell subsets were Th1 cells and cytotoxic T lymphocytes (CTLs), implying the potentially high cellular immune response. To verifying whether the prepared CAR-T cells were exhausted, the expression of several immune checkpoint markers was determined. Of interest, only less than 20% of CAR-T cells at endpoint were PD-1+ or CTLA4+, but more than 40% of CAR-T cells at the endpoint were TIM-3+, implying most CAR-T cells were not exhausted. These CAR-T cells produced more than 1 ng/mL of IFN-γ in the response to the antigen. Altogether, CAR-T cells could be prepared in our serum-free process in the controlling of T cell subsets, leading to potential high therapeutic potency. Please click Additional Files below to see the full abstract