Adsorption of mono- and multivalent cat- and anions on DNA molecules

Adsorption of monovalent and multivalent cat- and anions on a deoxyribose nucleic acid (DNA) molecule from a salt solution is investigated by computer simulation. The ions are modelled as charged hard spheres, the DNA molecule as a point charge pattern following the double-helical phosphate strands. The geometrical shape of the DNA molecules is modelled on different levels ranging from a simple cylindrical shape to structured models which include the major and minor grooves between the phosphate strands. The densities of the ions adsorbed on the phosphate strands, in the major and in the minor grooves are calculated. First, we find that the adsorption pattern on the DNA surface depends strongly on its geometrical shape: counterions adsorb preferentially along the phosphate strands for a cylindrical model shape, but in the minor groove for a geometrically structured model. Second, we find that an addition of monovalent salt ions results in an increase of the charge density in the minor groove while the total charge density of ions adsorbed in the major groove stays unchanged. The adsorbed ion densities are highly structured along the minor groove while they are almost smeared along the major groove. Furthermore, for a fixed amount of added salt, the major groove cationic charge is independent on the counterion valency. For increasing salt concentration the major groove is neutralized while the total charge adsorbed in the minor groove is constant. DNA overcharging is detected for multivalent salt. Simulations for a larger ion radii, which mimic the effect of the ion hydration, indicate an increased adsorbtion of cations in the major groove.Comment: 34 pages with 14 figure

Heavy quarkonium: progress, puzzles, and opportunities

A golden age for heavy quarkonium physics dawned a decade ago, initiated by the confluence of exciting advances in quantum chromodynamics (QCD) and an explosion of related experimental activity. The early years of this period were chronicled in the Quarkonium Working Group (QWG) CERN Yellow Report (YR) in 2004, which presented a comprehensive review of the status of the field at that time and provided specific recommendations for further progress. However, the broad spectrum of subsequent breakthroughs, surprises, and continuing puzzles could only be partially anticipated. Since the release of the YR, the BESII program concluded only to give birth to BESIII; the $B$-factories and CLEO-c flourished; quarkonium production and polarization measurements at HERA and the Tevatron matured; and heavy-ion collisions at RHIC have opened a window on the deconfinement regime. All these experiments leave legacies of quality, precision, and unsolved mysteries for quarkonium physics, and therefore beg for continuing investigations. The plethora of newly-found quarkonium-like states unleashed a flood of theoretical investigations into new forms of matter such as quark-gluon hybrids, mesonic molecules, and tetraquarks. Measurements of the spectroscopy, decays, production, and in-medium behavior of c\bar{c}, b\bar{b}, and b\bar{c} bound states have been shown to validate some theoretical approaches to QCD and highlight lack of quantitative success for others. The intriguing details of quarkonium suppression in heavy-ion collisions that have emerged from RHIC have elevated the importance of separating hot- and cold-nuclear-matter effects in quark-gluon plasma studies. This review systematically addresses all these matters and concludes by prioritizing directions for ongoing and future efforts.Comment: 182 pages, 112 figures. Editors: N. Brambilla, S. Eidelman, B. K. Heltsley, R. Vogt. Section Coordinators: G. T. Bodwin, E. Eichten, A. D. Frawley, A. B. Meyer, R. E. Mitchell, V. Papadimitriou, P. Petreczky, A. A. Petrov, P. Robbe, A. Vair

Soil microbes and their response to experimental warming over time: A meta-analysis of field studies

Numerous field studies have found changes in soil respiration and microbial abundance under experimental warming. Yet, it is uncertain whether the magnitude of these responses remains consistent over the long-term. We performed a meta-analysis on 25 field experiments to examine how warming effects on soil respiration, microbial biomass, and soil microbial C respond to the duration of warming. For each parameter, we hypothesized that effect sizes of warming would diminish as the duration of warming increased. In support of our hypothesis, warming initially increased soil respiration, but the magnitude of this effect declined significantly as warming progressed as evidenced by the two longest studies in our meta-analysis. In fact, after 10 years of warming, soil respiration in warmed treatments was similar to controls. In contrast, warming effect sizes for fungal biomass, bacterial biomass, and soil microbial C did not respond significantly to the duration of warming. Microbial acclimation, community shifts, adaptation, or reductions in labile C may have ameliorated warming effects on soil respiration in the long-term. Accordingly, long-term soil C losses might be smaller than those suggested by short-term warming studies

Measurements of Ξ(1530)0{\Xi \left( 1530\right) ^{0}} and Ξ‾(1530)0{\overline{\Xi }\left( 1530\right) ^{0}} production in proton–proton interactions at sNN\sqrt{s_{NN}} = 17.3 = 17.3 GeV \text{ GeV } in the NA61/SHINE experiment

Double-differential yields of $\Xi\left(1530\right)^{0}$ and $\overline{\Xi}\left(1530\right)^{0}$ resonances produced in \pp interactions were measured at a laboratory beam momentum of 158~\GeVc. This measurement is the first of its kind in \pp interactions below LHC energies. It was performed at the CERN SPS by the \NASixtyOne collaboration. Double-differential distributions in rapidity and transverse momentum were obtained from a sample of 26$\cdot$10$^6$ inelastic events. The spectra are extrapolated to full phase space resulting in mean multiplicity of $\Xi\left(1530\right)^{0}$ (6.73 $\pm$ 0.25 $\pm$ 0.67)$\times10^{-4}$ and $\overline{\Xi}\left(1530\right)^{0}$ (2.71 $\pm$ 0.18 $\pm$ 0.18)$\times10^{-4}$. The rapidity and transverse momentum spectra and mean multiplicities were compared to predictions of string-hadronic and statistical model calculations

Measurements of Ξ−{\Xi }{^-} and Ξ‾+\overline{\Xi }{^+} production in proton–proton interactions at sNN\sqrt{s_{NN}}=17.3 GeV = 17.3 GeV in the NA61/SHINE experiment

International audienceThe production of $\Xi (1321)^{-}$ and $\overline{\Xi }(1321)^{+}$ hyperons in inelastic p+p interactions is studied in a fixed target experiment at a beam momentum of 158 $\hbox {Ge}\hbox {V}\!/\!c$. Double differential distributions in rapidity ${y}$ and transverse momentum $p_{T}$ are obtained from a sample of 33M inelastic events. They allow to extrapolate the spectra to full phase space and to determine the mean multiplicity of both ${\Xi }{^-}$ and $\overline{\Xi }{^+}$. The rapidity and transverse momentum spectra are compared to transport model predictions. The ${\Xi }{^-}$ mean multiplicity in inelastic p+p interactions at 158 $\hbox {Ge}\hbox {V}\!/\!c$ is used to quantify the strangeness enhancement in A+A collisions at the same centre-of-mass energy per nucleon pair

A new strategy for enhancing imputation quality of rare variants from next-generation sequencing data via combining SNP and exome chip data

Background: Rare variants have gathered increasing attention as a possible alternative source of missing heritability. Since next generation sequencing technology is not yet cost-effective for large-scale genomic studies, a widely used alternative approach is imputation. However, the imputation approach may be limited by the low accuracy of the imputed rare variants. To improve imputation accuracy of rare variants, various approaches have been suggested, including increasing the sample size of the reference panel, using sequencing data from study-specific samples (i.e., specific populations), and using local reference panels by genotyping or sequencing a subset of study samples. While these approaches mainly utilize reference panels, imputation accuracy of rare variants can also be increased by using exome chips containing rare variants. The exome chip contains 250 K rare variants selected from the discovered variants of about 12,000 sequenced samples. If exome chip data are available for previously genotyped samples, the combined approach using a genotype panel of merged data, including exome chips and SNP chips, should increase the imputation accuracy of rare variants. Results: In this study, we describe a combined imputation which uses both exome chip and SNP chip data simultaneously as a genotype panel. The effectiveness and performance of the combined approach was demonstrated using a reference panel of 848 samples constructed using exome sequencing data from the T2D-GENES consortium and 5,349 sample genotype panels consisting of an exome chip and SNP chip. As a result, the combined approach increased imputation quality up to 11 %, and genomic coverage for rare variants up to 117.7 % (MAF < 1 %), compared to imputation using the SNP chip alone. Also, we investigated the systematic effect of reference panels on imputation quality using five reference panels and three genotype panels. The best performing approach was the combination of the study specific reference panel and the genotype panel of combined data. Conclusions: Our study demonstrates that combined datasets, including SNP chips and exome chips, enhances both the imputation quality and genomic coverage of rare variants

Application of a risk-management framework for integration of stromal tumor-infiltrating lymphocytes in clinical trials

Stromal tumor-infiltrating lymphocytes (sTILs) are a potential predictive biomarker for immunotherapy response in metastatic triple-negative breast cancer (TNBC). To incorporate sTILs into clinical trials and diagnostics, reliable assessment is essential. In this review, we propose a new concept, namely the implementation of a risk-management framework that enables the use of sTILs as a stratification factor in clinical trials. We present the design of a biomarker risk-mitigation workflow that can be applied to any biomarker incorporation in clinical trials. We demonstrate the implementation of this concept using sTILs as an integral biomarker in a single-center phase II immunotherapy trial for metastatic TNBC (TONIC trial, NCT02499367), using this workflow to mitigate risks of suboptimal inclusion of sTILs in this specific trial. In this review, we demonstrate that a web-based scoring platform can mitigate potential risk factors when including sTILs in clinical trials, and we argue that this framework can be applied for any future biomarker-driven clinical trial setting

A search for the decay B+→K+ννˉB^+ \to K^+ \nu \bar{\nu}

We search for the rare flavor-changing neutral-current decay $B^+ \to K^+ \nu \bar{\nu}$ in a data sample of 82 fb$^{-1}$ collected with the {\sl BABAR} detector at the PEP-II B-factory. Signal events are selected by examining the properties of the system recoiling against either a reconstructed hadronic or semileptonic charged-B decay. Using these two independent samples we obtain a combined limit of ${\mathcal B}(B^+ \to K^+ \nu \bar{\nu})<5.2 \times 10^{-5}$ at the 90% confidence level. In addition, by selecting for pions rather than kaons, we obtain a limit of ${\mathcal B}(B^+ \to \pi^+ \nu \bar{\nu})<1.0 \times 10^{-4}$ using only the hadronic B reconstruction method.Comment: 7 pages, 8 postscript figures, submitted to Phys. Rev. Let