1,177 research outputs found
Rapid detection of adulterated drugs in herbal dietary supplements by wooden-tip electrospray ionization mass spectrometry
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Magnetism and Charge Dynamics in Iron Pnictides
In a wide variety of materials, such as copper oxides, heavy fermions,
organic salts, and the recently discovered iron pnictides, superconductivity is
found in close proximity to a magnetically ordered state. The character of the
proximate magnetic phase is thus believed to be crucial for understanding the
differences between the various families of unconventional superconductors and
the mechanism of superconductivity. Unlike the AFM order in cuprates, the
nature of the magnetism and of the underlying electronic state in the iron
pnictide superconductors is not well understood. Neither density functional
theory nor models based on atomic physics and superexchange, account for the
small size of the magnetic moment. Many low energy probes such as transport,
STM and ARPES measured strong anisotropy of the electronic states akin to the
nematic order in a liquid crystal, but there is no consensus on its physical
origin, and a three dimensional picture of electronic states and its relations
to the optical conductivity in the magnetic state is lacking. Using a first
principles approach, we obtained the experimentally observed magnetic moment,
optical conductivity, and the anisotropy of the electronic states. The theory
connects ARPES, which measures one particle electronic states, optical
spectroscopy, probing the particle hole excitations of the solid and neutron
scattering which measures the magnetic moment. We predict a manifestation of
the anisotropy in the optical conductivity, and we show that the magnetic phase
arises from the paramagnetic phase by a large gain of the Hund's rule coupling
energy and a smaller loss of kinetic energy, indicating that iron pnictides
represent a new class of compounds where the nature of magnetism is
intermediate between the spin density wave of almost independent particles, and
the antiferromagnetic state of local moments.Comment: 4+ pages with additional one-page supplementary materia
Kinetic frustration and the nature of the magnetic and paramagnetic states in iron pnictides and iron chalcogenides
The iron pnictide and chalcogenide compounds are a subject of intensive
investigations due to their high temperature superconductivity.\cite{a-LaFeAsO}
They all share the same structure, but there is significant variation in their
physical properties, such as magnetic ordered moments, effective masses,
superconducting gaps and T. Many theoretical techniques have been applied
to individual compounds but no consistent description of the trends is
available \cite{np-review}. We carry out a comparative theoretical study of a
large number of iron-based compounds in both their magnetic and paramagnetic
states. We show that the nature of both states is well described by our method
and the trends in all the calculated physical properties such as the ordered
moments, effective masses and Fermi surfaces are in good agreement with
experiments across the compounds. The variation of these properties can be
traced to variations in the key structural parameters, rather than changes in
the screening of the Coulomb interactions. Our results provide a natural
explanation of the strongly Fermi surface dependent superconducting gaps
observed in experiments\cite{Ding}. We propose a specific optimization of the
crystal structure to look for higher T superconductors.Comment: 5 pages, 3 figures with a 5-page supplementary materia
Molecular Valves for Controlling Gas Phase Transport Made from Discrete Angstrom-Sized Pores in Graphene
An ability to precisely regulate the quantity and location of molecular flux
is of value in applications such as nanoscale 3D printing, catalysis, and
sensor design. Barrier materials containing pores with molecular dimensions
have previously been used to manipulate molecular compositions in the gas
phase, but have so far been unable to offer controlled gas transport through
individual pores. Here, we show that gas flux through discrete angstrom-sized
pores in monolayer graphene can be detected and then controlled using
nanometer-sized gold clusters, which are formed on the surface of the graphene
and can migrate and partially block a pore. In samples without gold clusters,
we observe stochastic switching of the magnitude of the gas permeance, which we
attribute to molecular rearrangements of the pore. Our molecular valves could
be used, for example, to develop unique approaches to molecular synthesis that
are based on the controllable switching of a molecular gas flux, reminiscent of
ion channels in biological cell membranes and solid state nanopores.Comment: to appear in Nature Nanotechnolog
Glycoprotein Ib activation by thrombin stimulates the energy metabolism in human platelets
<div><p>Thrombin-induced platelet activation requires substantial amounts of ATP. However, the specific contribution of each ATP-generating pathway <i>i</i>.<i>e</i>., oxidative phosphorylation (OxPhos) versus glycolysis and the biochemical mechanisms involved in the thrombin-induced activation of energy metabolism remain unclear. Here we report an integral analysis on the role of both energy pathways in human platelets activated by several agonists, and the signal transducing mechanisms associated with such activation. We found that thrombin, Trap-6, arachidonic acid, collagen, A23187, epinephrine and ADP significantly increased glycolytic flux (3–38 times <i>vs</i>. non-activated platelets) whereas ristocetin was ineffective. OxPhos (33 times) and mitochondrial transmembrane potential (88%) were increased only by thrombin. OxPhos was the main source of ATP in thrombin-activated platelets, whereas in platelets activated by any of the other agonists, glycolysis was the principal ATP supplier. In order to establish the biochemical mechanisms involved in the thrombin-induced OxPhos activation in platelets, several signaling pathways associated with mitochondrial activation were analyzed. Wortmannin and LY294002 (PI3K/Akt pathway inhibitors), ristocetin and heparin (GPIb inhibitors) as well as resveratrol, ATP (calcium-release inhibitors) and PP1 (Tyr-phosphorylation inhibitor) prevented the thrombin-induced platelet activation. These results suggest that thrombin activates OxPhos and glycolysis through GPIb-dependent signaling involving PI3K and Akt activation, calcium mobilization and protein phosphorylation.</p></div
Observation of a ppb mass threshoud enhancement in \psi^\prime\to\pi^+\pi^-J/\psi(J/\psi\to\gamma p\bar{p}) decay
The decay channel
is studied using a sample of events collected
by the BESIII experiment at BEPCII. A strong enhancement at threshold is
observed in the invariant mass spectrum. The enhancement can be fit
with an -wave Breit-Wigner resonance function with a resulting peak mass of
and a
narrow width that is at the 90% confidence level.
These results are consistent with published BESII results. These mass and width
values do not match with those of any known meson resonance.Comment: 5 pages, 3 figures, submitted to Chinese Physics
Frequent Heterogeneous Missense Mutations of GGAP2 in Prostate Cancer: Implications for Tumor Biology, Clonality and Mutation Analysis
Prostate cancer is the most common visceral malignancy in Western men and a major cause of cancer deaths. Increased activation of the AKT and NFkB pathways have been identified as critical steps in prostate cancer initiation and progression. GGAP2 (GTP-binding and GTPase activating protein 2) is a multidomain protein that contains an N-terminal Ras homology domain (GTPase), followed by a PH domain, a C-terminal GAP domain and an ankyrin repeat domain. GGAP2 can directly activate signaling via both the AKT and NFkB pathways and acts as a node of crosstalk between these pathways. Increased GGAP2 expression is present in three quarters of prostate cancers. Mutations of GGAP2 have been reported in cell lines from other malignancies. We therefore analyzed 84 prostate cancer tissues and 43 benign prostate tissues for somatic mutations in GGAP2 by direct sequencing of individual clones derived from the GAP and GTPase domains of normal and tumor tissue. Overall, half of cancers contained mutant GAP domain clones and in 20% of cancers, 30% or more of clones were mutant in the GAP domain. Surprisingly, the mutations were heterogeneous and nonclonal, with multiple different mutations being present in many tumors. Similar findings were observed in the analysis of the GTPase domain. Mutant GGAP2 proteins had significantly higher transcriptional activity using AP-1 responsive reporter constructs when compared to wild-type protein. Furthermore, the presence of these mutations was associated with aggressive clinical behavior. The presence of high frequency nonclonal mutations of a single gene is novel and represents a new mode of genetic alteration that can promote tumor progression. Analysis of mutations in cancer has been used to predict outcome and guide therapeutic target identification but such analysis has focused on clonal mutations. Our studies indicate that in some cases high frequency nonclonal mutations may need to be assessed as well
Non-Parametric Change-Point Method for Differential Gene Expression Detection
We proposed a non-parametric method, named Non-Parametric Change Point
Statistic (NPCPS for short), by using a single equation for detecting
differential gene expression (DGE) in microarray data. NPCPS is based on the
change point theory to provide effective DGE detecting ability.NPCPS used the data distribution of the normal samples as input, and detects
DGE in the cancer samples by locating the change point of gene expression
profile. An estimate of the change point position generated by NPCPS enables
the identification of the samples containing DGE. Monte Carlo simulation and
ROC study were applied to examine the detecting accuracy of NPCPS, and the
experiment on real microarray data of breast cancer was carried out to
compare NPCPS with other methods.Simulation study indicated that NPCPS was more effective for detecting DGE in
cancer subset compared with five parametric methods and one non-parametric
method. When there were more than 8 cancer samples containing DGE, the type
I error of NPCPS was below 0.01. Experiment results showed both good
accuracy and reliability of NPCPS. Out of the 30 top genes ranked by using
NPCPS, 16 genes were reported as relevant to cancer. Correlations between
the detecting result of NPCPS and the compared methods were less than 0.05,
while between the other methods the values were from 0.20 to 0.84. This
indicates that NPCPS is working on different features and thus provides DGE
identification from a distinct perspective comparing with the other mean or
median based methods
Heterostructured electrode with concentration gradient shell for highly efficient oxygen reduction at low temperature
Heterostructures of oxides have been widely investigated in optical, catalytic and electrochemical applications, because the heterostructured interfaces exhibit pronouncedly different transport, charge, and reactivity characteristics compared to the bulk of the oxides. Here we fabricated a three-dimensional (3D) heterostructured electrode with a concentration gradient shell. The concentration gradient shell with the composition of Ba0.5-xSr0.5-yCo0.8Fe0.2O3-δ (BSCF-D) was prepared by simply treating porous Ba0.5Sr0.5Co0.8Fe0.2O3-δ (BSCF) backbone with microwave-plasma. Electrochemical impedance spectroscopy reveals that the oxygen surface exchange rate of the BSCF-D is enhanced by ~250% that of the pristine BSCF due to the appearance of the shell. The heterostructured electrode shows an interfacial resistance as low as 0.148 Ω cm2 at 550°C and an unchanged electrochemical performance after heating treatment for 200 h. This method offers potential to prepare heterostructured oxides not only for electrochemical devices but also for many other applications that use ceramic materials
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