6,131 research outputs found
Optical Studies of Metal- Semiconductor Transmutations Produced by Intercalation
Spectra of the alkali metal intercalation products of MoS2 and NbSc2 arc interpreted in terms of a previously published band model
Uncovering the Mechanism of Aggregation of Human Transthyretin.
The tetrameric thyroxine transport protein transthyretin (TTR) forms amyloid fibrils upon dissociation and monomer unfolding. The aggregation of transthyretin has been reported as the cause of the life-threatening transthyretin amyloidosis. The standard treatment of familial cases of TTR amyloidosis has been liver transplantation. Although aggregation-preventing strategies involving ligands are known, understanding the mechanism of TTR aggregation can lead to additional inhibition approaches. Several models of TTR amyloid fibrils have been proposed, but the segments that drive aggregation of the protein have remained unknown. Here we identify β-strands F and H as necessary for TTR aggregation. Based on the crystal structures of these segments, we designed two non-natural peptide inhibitors that block aggregation. This work provides the first characterization of peptide inhibitors for TTR aggregation, establishing a novel therapeutic strategy
Effective affinities in microarray data
In the past couple of years several studies have shown that hybridization in
Affymetrix DNA microarrays can be rather well understood on the basis of simple
models of physical chemistry. In the majority of the cases a Langmuir isotherm
was used to fit experimental data. Although there is a general consensus about
this approach, some discrepancies between different studies are evident. For
instance, some authors have fitted the hybridization affinities from the
microarray fluorescent intensities, while others used affinities obtained from
melting experiments in solution. The former approach yields fitted affinities
that at first sight are only partially consistent with solution values. In this
paper we show that this discrepancy exists only superficially: a sufficiently
complete model provides effective affinities which are fully consistent with
those fitted to experimental data. This link provides new insight on the
relevant processes underlying the functioning of DNA microarrays.Comment: 8 pages, 6 figure
IMAGES I. Strong evolution of galaxy kinematics since z=1
(abbreviated) We present the first results of the ESO large program,
``IMAGES'' which aims at obtaining robust measurements of the kinematics of
distant galaxies using the multi-IFU mode of GIRAFFE on the VLT. 3D
spectroscopy is essential to robustly measure the often distorted kinematics of
distant galaxies (e.g., Flores et al. 2006). We derive the velocity fields and
-maps of 36 galaxies at 0.4<z<0.75 from the kinematics of the [OII]
emission line doublet, and generate a robust technique to identify the nature
of the velocity fields based on the pixels of the highest signal-to-noise
ratios (S/N). We have gathered a unique sample of 63 velocity fields of
emission line galaxies (W0([OII]) > 15 A) at z=0.4-0.75, which are a
representative subsample of the population of M_stellar>1.5x10^{10} M_sun
emission line galaxies in this redshift range, and are largely unaffected by
cosmic variance. Taking into account all galaxies -with or without emission
lines- in that redshift range, we find that at least 41+/-7% of them have
anomalous kinematics, i.e., they are not dynamically relaxed. This includes
26+/-7% of distant galaxies with complex kinematics, i.e., they are not simply
pressure or rotationally supported. Our result implies that galaxy kinematics
are among the most rapidly evolving properties, because locally, only a few
percent of the galaxies in this mass range have complex kinematics.Comment: 17 pages, 6 figures, Accepted by A&
Electronic structure of Co_xTiSe_2 and Cr_xTiSe_2
The results of investigations of intercalated compounds Cr_xTiSe_2 and
Co_xTiSe_2 by X-ray photoelectron spectroscopy (XPS) and X-ray emission
spectroscopy (XES) are presented. The data obtained are compared with
theoretical results of spin-polarized band structure calculations. A good
agreement between theoretical and experimental data for the electronic
structure of the investigated materials has been observed. The interplay
between the M3d--Ti3d hybridization (M=Cr, Co) and the magnetic moment at the M
site is discussed. A 0.9 eV large splitting of the core Cr2p{3/2} level was
observed, which reveals a strong exchange magnetic interaction of 3d-2p
electrons of Cr. In the case of a strong localization of the Cr3d electrons
(for x<0.25), the broadening of the CrL spectra into the region of the states
above the nominal Fermi level was observed and attributed to X-ray re-emission.
The measured kinetic properties are in good accordance with spectral
investigations and band calculation results.Comment: 14 pages, 11 figures, submitted to Phys.Rev.
Observation of Dirac Node Formation and Mass Acquisition in a Topological Crystalline Insulator
In topological crystalline insulators (TCIs), topology and crystal symmetry intertwine to create surface states with distinct characteristics. The breaking of crystal symmetry in TCIs is predicted to impart mass to the massless Dirac fermions. Here, we report high-resolution scanning tunneling microscopy studies of a TCI, Pb1-xSnxSe that reveal the coexistence of zero-mass Dirac fermions protected by crystal symmetry with massive Dirac fermions consistent with crystal symmetry breaking. In addition, we show two distinct regimes of the Fermi surface topology separated by a Van-Hove singularity at the Lifshitz transition point. Our work paves the way for engineering the Dirac band gap and realizing interaction-driven topological quantum phenomena in TCIs
Critical scaling of the a.c. conductivity for a superconductor above Tc
We consider the effects of critical superconducting fluctuations on the
scaling of the linear a.c. conductivity, \sigma(\omega), of a bulk
superconductor slightly above Tc in zero applied magnetic field. The dynamic
renormalization- group method is applied to the relaxational time-dependent
Ginzburg-Landau model of superconductivity, with \sigma(\omega) calculated via
the Kubo formula to O(\epsilon^{2}) in the \epsilon = 4 - d expansion. The
critical dynamics are governed by the relaxational XY-model
renormalization-group fixed point. The scaling hypothesis \sigma(\omega) \sim
\xi^{2-d+z} S(\omega \xi^{z}) proposed by Fisher, Fisher and Huse is explicitly
verified, with the dynamic exponent z \approx 2.015, the value expected for the
d=3 relaxational XY-model. The universal scaling function S(y) is computed and
shown to deviate only slightly from its Gaussian form, calculated earlier. The
present theory is compared with experimental measurements of the a.c.
conductivity of YBCO near Tc, and the implications of this theory for such
experiments is discussed.Comment: 16 pages, submitted to Phys. Rev.
Rheumatoid synovial fluid interleukin-17-producing CD4 T cells have abundant tumor necrosis factor-alpha co-expression, but little interleukin-22 and interleukin-23R expression
Introduction\ud
Th17 cells have been implicated in the pathogenesis of rheumatoid arthritis (RA). The aim of this study was to systematically analyse the phenotype, cytokine profile and frequency of interleukin-17 (IL-17) producing CD4-positive T cells in mononuclear cells isolated from peripheral blood, synovial fluid and synovial tissue of RA patients with established disease, and to correlate cell frequencies with disease activity. \ud
\ud
Methods\ud
Flow cytometry was used to analyse the phenotype and cytokine production of mononuclear cells isolated from peripheral blood (PBMC) (n = 44), synovial fluid (SFMC) (n = 14) and synovium (SVMC) (n = 10) of RA patients and PBMC of healthy controls (n = 13). \ud
\ud
Results\ud
The frequency of IL-17-producing CD4 T cells was elevated in RA SFMC compared with RA PBMC (P = 0.04). However, the frequency of this population in RA SVMC was comparable to that in paired RA PBMC. The percentage of IL-17-producing CD4 T cells coexpressing tumor necrosis factor alpha (TNFα) was significantly increased in SFMC (P = 0.0068). The frequency of IFNγ-producing CD4 T cells was also significantly higher in SFMC than paired PBMC (P = 0.042). The majority of IL-17-producing CD4 T cells coexpressed IFNγ. IL-17-producing CD4 T cells in RA PBMC and SFMC exhibited very little IL-22 or IL-23R coexpression. \ud
\ud
Conclusions\ud
These findings demonstrate a modest enrichment of IL-17-producing CD4 T cells in RA SFMC compared to PBMC. Th17 cells in SFMC produce more TNFα than their PBMC counterparts, but are not a significant source of IL-22 and do not express IL-23R. However, the percentage of CD4 T cells which produce IL-17 in the rheumatoid joint is low, suggesting that other cells may be alternative sources of IL-17 within the joints of RA patients. \ud
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Anastral spindle assembly and γ-tubulin in Drosophila oocytes
<p>Abstract</p> <p>Background</p> <p>Anastral spindles assemble by a mechanism that involves microtubule nucleation and growth from chromatin. It is still uncertain whether γ-tubulin, a microtubule nucleator essential for mitotic spindle assembly and maintenance, plays a role. Not only is the requirement for γ-tubulin to form anastral <it>Drosophila </it>oocyte meiosis I spindles controversial, but its presence in oocyte meiosis I spindles has not been demonstrated and is uncertain.</p> <p>Results</p> <p>We show, for the first time, using a bright GFP fusion protein and live imaging, that the <it>Drosophila </it>maternally-expressed γTub37C is present at low levels in oocyte meiosis I spindles. Despite this, we find that formation of bipolar meiosis I spindles does not require functional γTub37C, extending previous findings by others. Fluorescence photobleaching assays show rapid recovery of γTub37C in the meiosis I spindle, similar to the cytoplasm, indicating weak binding by γTub37C to spindles, and fits of a new, potentially more accurate model for fluorescence recovery yield kinetic parameters consistent with transient, diffusional binding.</p> <p>Conclusions</p> <p>The FRAP results, together with its mutant effects late in meiosis I, indicate that γTub37C may perform a role subsequent to metaphase I, rather than nucleating microtubules for meiosis I spindle formation. Weak binding to the meiosis I spindle could stabilize pre-existing microtubules or position γ-tubulin for function during meiosis II spindle assembly, which follows rapidly upon oocyte activation and completion of the meiosis I division.</p
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