273 research outputs found
Low temperature structural effects in the (TMTSF)PF and AsF Bechgaard salts
We present a detailed low-temperature investigation of the statics and
dynamics of the anions and methyl groups in the organic conductors
(TMTSF)PF and (TMTSF)AsF (TMTSF :
tetramethyl-tetraselenafulvalene). The 4 K neutron scattering structure
refinement of the fully deuterated (TMTSF)PF-D12 salt allows locating
precisely the methyl groups at 4 K. This structure is compared to the one of
the fully hydrogenated (TMTSF)PF-H12 salt previously determined at the
same temperature. Surprisingly it is found that deuteration corresponds to the
application of a negative pressure of 5 x 10 MPa to the H12 salt. Accurate
measurements of the Bragg intensity show anomalous thermal variations at low
temperature both in the deuterated PF and AsF salts. Two different
thermal behaviors have been distinguished. Low-Bragg-angle measurements reflect
the presence of low-frequency modes at characteristic energies {\theta} =
8.3 K and {\theta} = 6.7 K for the PF-D12 and AsF-D12 salts,
respectively. These modes correspond to the low-temperature methyl group
motion. Large-Bragg-angle measurements evidence an unexpected structural change
around 55 K which probably corresponds to the linkage of the anions to the
methyl groups via the formation of F...D-CD2 bonds observed in the 4 K
structural refinement. Finally we show that the thermal expansion coefficient
of (TMTSF)PF is dominated by the librational motion of the PF
units. We quantitatively analyze the low-temperature variation of the lattice
expansion via the contribution of Einstein oscillators, which allows us to
determine for the first time the characteristic frequency of the PF6
librations: {\theta} = 50 K and {\theta} = 76 K for the PF-D12 and
PF-H12 salts, respectively
Structural aspects of the metal-insulator transition in BaVS3
A sequence of structural transitions occurring in the quasi-one-dimensional
(1D) 3d1 system BaVS3 at low temperature was investigated by high resolution
synchrotron X-ray diffraction. The orthorhombic Cmc21 structure of the
intermediate-temperature (70K<T<240K) phase was confirmed. A model for the
low-T (T<70K) k=(1 0 1/2)O superstructure (with Im symmetry) is proposed and
refined. The formation of the superstructure is associated with the
stabilization of a mixed bond order / charge density wave
Near-Edge X‐ray Absorption Fine Structure Investigation of the Quasi-One-Dimensional Organic Conductor (TMTSF)2PF6
We present high-resolution near-edge X-ray absorption fine structure (NEXAFS) measurements at the P L2/3 edges, F K edge, C K edge, and Se M2/3 edges of the quasi-one-dimensional (1D) conductor and superconductor (TMTSF)2PF6. NEXAFS allows probing the donor and acceptor moieties separately; spectra were recorded between room temperature (RT) and 30 K at normal incidence. Spectra taken around RT were also studied as a function of the angle (θ) between the electric field of the X-ray beam and the 1D conducting direction. In contrast with a previous study of the S L2/3-edges spectra in (TMTTF)2AsF6, the Se M2/3 edges of (TMTSF)2PF6 do not exhibit a well-resolved spectrum. Surprisingly, the C K-edge spectra contain three well-defined peaks exhibiting strong and nontrivial θ and temperature dependence. The nature of these peaks as well as those of the F K-edge spectra could be rationalized on the basis of first-principles DFT calculations. Despite the structural similarity, the NEXAFS spectra of (TMTSF)2PF6 and (TMTTF)2AsF6 exhibit important differences. In contrast with the case of (TMTTF)2AsF6, the F K-edge spectra of (TMTSF)2PF6 do not change with temperature despite stronger donor−anion interactions. All these features reveal subtle differences in the electronic structure of the TMTSF and TMTTF families of salts
A new quantum fluid at high magnetic fields in the marginal charge-density-wave system -(BEDT-TTF)Hg(SCN) (where ~K and Rb)
Single crystals of the organic charge-transfer salts
-(BEDT-TTF)Hg(SCN) have been studied using Hall-potential
measurements (K) and magnetization experiments ( = K, Rb). The data show
that two types of screening currents occur within the high-field,
low-temperature CDW phases of these salts in response to time-dependent
magnetic fields. The first, which gives rise to the induced Hall potential, is
a free current (), present at the surface of the sample.
The time constant for the decay of these currents is much longer than that
expected from the sample resistivity. The second component of the current
appears to be magnetic (), in that it is a microscopic,
quasi-orbital effect; it is evenly distributed within the bulk of the sample
upon saturation. To explain these data, we propose a simple model invoking a
new type of quantum fluid comprising a CDW coexisting with a two-dimensional
Fermi-surface pocket which describes the two types of current. The model and
data are able to account for the body of previous experimental data which had
generated apparently contradictory interpretations in terms of the quantum Hall
effect or superconductivity.Comment: 13 pages, 11 figure
Interaction-induced Fermi surface deformations in quasi one-dimensional electronic systems
We consider serious conceptual problems with the application of standard
perturbation theory, in its zero temperature version, to the computation of the
dressed Fermi surface for an interacting electronic system. In order to
overcome these difficulties, we set up a variational approach which is shown to
be equivalent to the renormalized perturbation theory where the dressed Fermi
surface is fixed by recursively computed counterterms. The physical picture
that emerges is that couplings that are irrelevant tend to deform the Fermi
surface in order to become more relevant (irrelevant couplings being those that
do not exist at vanishing excitation energy because of kinematical constraints
attached to the Fermi surface). These insights are incorporated in a
renormalization group approach, which allows for a simple approximate
computation of Fermi surface deformation in quasi one-dimensional electronic
conductors. We also analyze flow equations for the effective couplings and
quasiparticle weights. For systems away from half-filling, the flows show three
regimes corresponding to a Luttinger liquid at high energies, a Fermi liquid,
and a low-energy incommensurate spin-density wave. At half-filling Umklapp
processes allow for a Mott insulator regime where the dressed Fermi surface is
flat, implying a confined phase with vanishing effective transverse
single-particle coherence. The boundary between the confined and Fermi liquid
phases is found to occur for a bare transverse hopping amplitude of the order
of the Mott charge gap of a single chain.Comment: 38 pages, 39 figures. Accepted for publication in Phys. Rev.
Pharmacological screening using an FXN-EGFP cellular genomic reporter assay for the therapy of Friedreich ataxia
Copyright @ 2013 Li et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.Friedreich ataxia (FRDA) is an autosomal recessive disorder characterized by neurodegeneration and cardiomyopathy. The presence of a GAA trinucleotide repeat expansion in the first intron of the FXN gene results in the inhibition of gene expression and an insufficiency of the mitochondrial protein frataxin. There is a correlation between expansion length, the amount of residual frataxin and the severity of disease. As the coding sequence is unaltered, pharmacological up-regulation of FXN expression may restore frataxin to therapeutic levels. To facilitate screening of compounds that modulate FXN expression in a physiologically relevant manner, we established a cellular genomic reporter assay consisting of a stable human cell line containing an FXN-EGFP fusion construct, in which the EGFP gene is fused in-frame with the entire normal human FXN gene present on a BAC clone. The cell line was used to establish a fluorometric cellular assay for use in high throughput screening (HTS) procedures. A small chemical library containing FDA-approved compounds and natural extracts was screened and analyzed. Compound hits identified by HTS were further evaluated by flow cytometry in the cellular genomic reporter assay. The effects on FXN mRNA and frataxin protein levels were measured in lymphoblast and fibroblast cell lines derived from individuals with FRDA and in a humanized GAA repeat expansion mouse model of FRDA. Compounds that were established to increase FXN gene expression and frataxin levels included several anti-cancer agents, the iron-chelator deferiprone and the phytoalexin resveratrol.Muscular Dystrophy Association (USA), the National Health and Medical Research Council (Australia), the Friedreich’s Ataxia Research Alliance (USA), the Brockhoff Foundation (Australia), the Friedreich Ataxia Research Association (Australasia), Seek A Miracle (USA) and the Victorian Government’s Operational Infrastructure Support Program
Generation and characterisation of Friedreich ataxia YG8R mouse fibroblast and neural stem cell models
This article has been made available through the Brunel Open Access Publishing Fund.Background: Friedreich ataxia (FRDA) is an autosomal recessive neurodegenerative disease caused by GAA repeat expansion in the first intron of the FXN gene, which encodes frataxin, an essential mitochondrial protein. To further characterise the molecular abnormalities associated with FRDA pathogenesis and to hasten drug screening, the development and use of animal and cellular models is considered essential. Studies of lower organisms have already contributed to understanding FRDA disease pathology, but mammalian cells are more related to FRDA patient cells in physiological terms. Methodology/Principal Findings: We have generated fibroblast cells and neural stem cells (NSCs) from control Y47R mice (9 GAA repeats) and GAA repeat expansion YG8R mice (190+120 GAA repeats). We then differentiated the NSCs in to neurons, oligodendrocytes and astrocytes as confirmed by immunocytochemical analysis of cell specific markers. The three YG8R mouse cell types (fibroblasts, NSCs and differentiated NSCs) exhibit GAA repeat stability, together with reduced expression of frataxin and reduced aconitase activity compared to control Y47R cells. Furthermore, YG8R cells also show increased sensitivity to oxidative stress and downregulation of Pgc-1α and antioxidant gene expression levels, especially Sod2. We also analysed various DNA mismatch repair (MMR) gene expression levels and found that YG8R cells displayed significant reduction in expression of several MMR genes, which may contribute to the GAA repeat stability. Conclusions/Significance: We describe the first fibroblast and NSC models from YG8R FRDA mice and we confirm that the NSCs can be differentiated into neurons and glia. These novel FRDA mouse cell models, which exhibit a FRDA-like cellular and molecular phenotype, will be valuable resources to further study FRDA molecular pathogenesis. They will also provide very useful tools for preclinical testing of frataxin-increasing compounds for FRDA drug therapy, for gene therapy, and as a source of cells for cell therapy testing in FRDA mice. © 2014 Sandi et al
Transcriptional responses of PBMC in psychosocially stressed animals indicate an alerting of the immune system in female but not castrated male pigs
Background[br/]
Brain and immune system are linked in a bi-directional manner. To date, it remained largely unknown why immune components become suppressed, enhanced, or remain unaffected in relation to psychosocial stress. Therefore, we mixed unfamiliar pigs with different levels of aggressiveness. We separated castrated male and female pigs into psychosocially high- and low- stressed animals by skin lesions, plasma cortisol level, and creatine kinase activity obtained from agonistic behaviour associated with regrouping. Peripheral blood mononuclear cells (PBMC) were collected post-mortem and differential gene expression was assessed using the Affymetrix platform (n = 16).[br/]
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Results[br/]
Relevant stress-dependent alterations were found only between female samples, but not between castrated male samples. Molecular routes related to TREM 1 signalling, dendritic cell maturation, IL-6 signalling, Toll-like receptor signalling, and IL-8 signalling were increased in high stressed females compared to low stressed females. This indicates a launch of immune effector molecules as a direct response. According to the shifts of transcripts encoding cell surface receptors (e.g. CD14, TLR2, TLR4, TREM1) the study highlights processes acting on pattern recognition, inflammation, and cell-cell communication.[br/]
[br/]
Conclusions[br/]
The transcriptional response partly affected the degree of ‘stress responsiveness’, indicating that the high stressed females altered their signal transduction due to potential infections and injuries while fighting
C-Terminal Extension of the Yeast Mitochondrial DNA Polymerase Determines the Balance between Synthesis and Degradation
Saccharomyces cerevisiae mitochondrial DNA polymerase (Mip1) contains a C-terminal extension (CTE) of 279 amino acid residues. The CTE is required for mitochondrial DNA maintenance in yeast but is absent in higher eukaryotes. Here we use recombinant Mip1 C-terminal deletion mutants to investigate functional importance of the CTE. We show that partial removal of the CTE in Mip1Δ216 results in strong preference for exonucleolytic degradation rather than DNA polymerization. This disbalance in exonuclease and polymerase activities is prominent at suboptimal dNTP concentrations and in the absence of correctly pairing nucleotide. Mip1Δ216 also displays reduced ability to synthesize DNA through double-stranded regions. Full removal of the CTE in Mip1Δ279 results in complete loss of Mip1 polymerase activity, however the mutant retains its exonuclease activity. These results allow us to propose that CTE functions as a part of Mip1 polymerase domain that stabilizes the substrate primer end at the polymerase active site, and is therefore required for efficient mitochondrial DNA replication in vivo
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