2,745 research outputs found
Strong mass effect on ion beam mixing in metal bilayers
Molecular dynamics simulations have been used to study the mechanism of ion
beam mixing in metal bilayers. We are able to explain the ion induced
low-temperature phase stability and melting behavior of bilayers using only a
simple ballistic picture up to 10 keV ion energies. The atomic mass ratio of
the overlayer and the substrate constituents seems to be a key quantity in
understanding atomic mixing. The critical bilayer mass ratio of
is required for the occurrence of a thermal spike (local melting) with a
lifetime of ps at low-energy ion irradiation (1 keV) due to a
ballistic mechanism. The existing experimental data follow the same trend as
the simulated values.Comment: 4 pages, 4 figures, preprin
Observations of the Cosmic Microwave Background and Galactic Foregrounds at 12-17 GHz with the COSMOSOMAS Experiment
(Abridged) We present the analysis of the first 18 months of data obtained
with the COSMOSOMAS experiment at the Teide Observatory (Tenerife). Three maps
have been obtained at 12.7, 14.7 and 16.3 GHz covering 9000 square degrees each
with a resolution of ~1 degree and with sensitivities 49, 59 and 115 muK per
beam respectively. These data in conjuction with the WMAP first year maps have
revealed that the Cosmic Microwave Background (CMB) is the dominant
astronomical signal at high galatic latitude in the three COSMOSOMAS channels
with an average amplitude of 29.7+/- 1.0 \muK (68% c.l. not including
calibration errors). This value is in agreement with the predicted CMB signal
in the COSMOSOMAS maps using the best fit Lambda-CDM model to the WMAP power
spectrum. Cross-correlation of COSMOSOMAS data with the DIRBE map at 100 \mu m
shows the existence of a common signal with amplitude 7.4+/- 1.1, 7.5+/- 1.1,
and 6.5+/-2.3 muK in the 12.7, 14.7 and 16.3 GHz COSMOSOMAS maps at
|b|>30^\deg. Using the WMAP data we find this DIRBE correlated signal rises
from high to low frequencies flattening below ~20 GHz. At higher galactic
latitudes the average amplitude of the correlated signal with the DIRBE maps
decreases slightly. The frequency behaviour of the COSMOSOMAS/WMAP correlated
signal with DIRBE is not compatible with the expected tendency for thermal
dust. A study of the H-alpha emission maps do not support free-free as a major
contributor to that signal. Our results provide evidence of a new galactic
foreground with properties compatible with those predicted by the spinning dust
models.Comment: 11 pages, 21 figures. Submitted to MNRAS. For paper with figures at
full resolution, see http://www.iac.es/project/cmb/cosmosomas
Deoxyribonucleic Acid as a Universal Electrolyte for Bio-Friendly Light-Emitting Electrochemical Cells [in press]
In the search for bio and eco‐friendly light sources, light‐emitting electrochemical cells (LECs) are promising candidates for the implementation of biomaterials in their device architecture thanks to their low fabrication complexity and wide range of potential technological applications. In this work, the use of the DNA derivative DNA‐cetyltrimethylammonium (DNA‐CTMA) is introduced as the ion‐solvating component of the solid polymer electrolyte (SPE) in the active layer of solution‐processed LECs. The focus is particularly on the investigation of its electrochemical and ionic conductivity properties demonstrating its suitability for device fabrication and correlation with thin film morphology. Furthermore, upon blending with the commercially available emissive polymer Super Yellow, the structure property relationship between the microstructure and the ionic conductivity is investigated and yields an optimized LEC performance. The large electrochemical stability window of DNA‐CTMA enables a stable device performance for a variety of emitters covering the complete visible spectral range, thus highlighting the universal character of this naturally sourced SPE
Molecular motors robustly drive active gels to a critically connected state
Living systems often exhibit internal driving: active, molecular processes
drive nonequilibrium phenomena such as metabolism or migration. Active gels
constitute a fascinating class of internally driven matter, where molecular
motors exert localized stresses inside polymer networks. There is evidence that
network crosslinking is required to allow motors to induce macroscopic
contraction. Yet a quantitative understanding of how network connectivity
enables contraction is lacking. Here we show experimentally that myosin motors
contract crosslinked actin polymer networks to clusters with a scale-free size
distribution. This critical behavior occurs over an unexpectedly broad range of
crosslink concentrations. To understand this robustness, we develop a
quantitative model of contractile networks that takes into account network
restructuring: motors reduce connectivity by forcing crosslinks to unbind.
Paradoxically, to coordinate global contractions, motor activity should be low.
Otherwise, motors drive initially well-connected networks to a critical state
where ruptures form across the entire network.Comment: Main text: 21 pages, 5 figures. Supplementary Information: 13 pages,
8 figure
Construction of a new class of tetracycline lead structures with potent antibacterial activity through biosynthetic engineering
Antimicrobial resistance and the shortage of novel antibiotics have led to an urgent need for new antibacterial drug leads. Several existing natural product scaffolds (including chelocardins) have not been developed because their suboptimal pharmacological properties could not be addressed at the time. It is demonstrated here that reviving such compounds through the application of biosynthetic engineering can deliver novel drug candidates. Through a rational approach, the carboxamido moiety of tetracyclines (an important structural feature for their bioactivity) was introduced into the chelocardins, which are atypical tetracyclines with an unknown mode of action. A broad-spectrum antibiotic lead was generated with significantly improved activity, including against all Gram-negative pathogens of the ESKAPE panel. Since the lead structure is also amenable to further chemical modification, it is a platform for further development through medicinal chemistry and genetic engineering
Prevalence of stroke and related burden among older people living in Latin America, India and China
Objectives Despite the growing importance of stroke in developing countries, little is known of stroke burden in survivors. the authors investigated the prevalence of self-reported stroke, stroke-related disability, dependence and care-giver strain in Latin America (LA), China and India.Methods Cross-sectional surveys were conducted on individuals aged 65+ (n=15 022) living in specified catchment areas. Self-reported stroke diagnosis, disability, care needs and care giver burden were assessed using a standardised protocol. for those reporting stroke, the correlates of disability, dependence and care-giver burden were estimated at each site using Poisson or linear regression, and combined meta-analytically.Results the prevalence of self-reported stroke ranged between 6% and 9% across most LA sites and urban China, but was much lower in urban India (1.9%), and in rural sites in India (1.1%), China (1.6%) and Peru (2.7%). the proportion of stroke survivors needing care varied between 20% and 39% in LA sites but was higher in rural China (44%), urban China (54%) and rural India (73%). Comorbid dementia and depression were the main correlates of disability and dependence.Conclusion the prevalence of stroke in urban LA and Chinese sites is nearly as high as in industrialised countries. High levels of disability and dependence in the other mainly rural and less-developed sites suggest underascertainment of less severe cases as one likely explanation for the lower prevalence in those settings. As the health transition proceeds, a further increase in numbers of older stroke survivors is to be anticipated. in addition to prevention, stroke rehabilitation and long-term care needs should be addressed.Wellcome TrustWorld Health Organization (India, Dominican Republic and China)US Alzheimer's AssociationFONACIT/ CDCH/ UCV (Venezuela)Kings Coll London, Inst Psychiat, Epidemiol Sect, Hlth Serv, London SE5 8AF, EnglandKings Coll London, Inst Psychiat, Clin Neurosci Div, London SE5 8AF, EnglandUniv Nacl Pedro Henriquez Urena, Geriatr Sect, Santo Domingo, Dominican RepUniv Peruana Cayetano Heredia, Lima, PeruPeking Univ, Inst Mental Hlth, Div Social Psychiat & Behav Med, Beijing 100871, Peoples R ChinaChristian Med Coll & Hosp, Vellore, Tamil Nadu, IndiaMed Univ Havana, Dept Clin Sci, Havana, CubaCaracas Univ Hosp, Dept Med, Caracas, VenezuelaNatl Inst Neurol & Neurosurg Mexico, Mexico City, DF, MexicoVHS, Dept Community Hlth, Chennai, Tamil Nadu, IndiaUniversidade Federal de São Paulo, Dept Psychiat, São Paulo, BrazilUniv Ciencias Med Matanzas, Dept Internal Med, Matanzas, CubaKings Coll London, Inst Psychiat, Epidemiol Sect, Populat Res Dept, London SE5 8AF, EnglandUniversidade Federal de São Paulo, Dept Psychiat, São Paulo, BrazilWellcome Trust: GR066133Wellcome Trust: GR08002US Alzheimer's Association: IIRG-04-1286Web of Scienc
Kinesin-1-mediated axonal transport of CB1 receptors is required for cannabinoid-dependent axonal growth and guidance
Endocannabinoids (eCB) modulate growth cone dynamics and axonal pathfinding through the stimulation of cannabinoid type-1 receptors (CB1R), the function of which depends on their delivery and precise presentation at the growth cone surface. However, the mechanism involved in the axonal transport of CB1R and its transport role in eCB signaling remains elusive. As mutations in the kinesin-1 molecular motor have been identified in patients with abnormal cortical development and impaired white matter integrity, we studied the defects in axonal pathfinding and fasciculation in mice lacking the kinesin light chain 1 (Klc1^-/-^) subunit of kinesin-1. Reduced levels of CB1R were found in corticofugal projections and axonal growth cones in Klc1^-/-^ mice. By live-cell imaging of CB1R-eGFP we characterized the axonal transport of CB1R vesicles and described the defects in transport that arise after KLC1 deletion. Cofilin activation, which is necessary for actin dynamics during growth cone remodeling, is impaired in the Klc1^-/-^ cerebral cortex. In addition, Klc1^-/-^ neurons showed expanded growth cones that were unresponsive to CB1R-induced axonal elongation. Together, our data reveal the relevance of kinesin-1 in CB1R axonal transport and in eCB signaling during brain wiring.Fil: Saez, Trinidad María de Los Milagros. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Biología Celular y Neurociencia "Prof. Eduardo de Robertis". Universidad de Buenos Aires. Facultad de Medicina. Instituto de Biología Celular y Neurociencia; ArgentinaFil: Fernandez Bessone, Iván. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Biología Celular y Neurociencia "Prof. Eduardo de Robertis". Universidad de Buenos Aires. Facultad de Medicina. Instituto de Biología Celular y Neurociencia; ArgentinaFil: Rodriguez, María S.. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Biología Celular y Neurociencia "Prof. Eduardo de Robertis". Universidad de Buenos Aires. Facultad de Medicina. Instituto de Biología Celular y Neurociencia; ArgentinaFil: Alloatti, Matías. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Biología Celular y Neurociencia "Prof. Eduardo de Robertis". Universidad de Buenos Aires. Facultad de Medicina. Instituto de Biología Celular y Neurociencia; ArgentinaFil: Otero, María G.. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Biología Celular y Neurociencia "Prof. Eduardo de Robertis". Universidad de Buenos Aires. Facultad de Medicina. Instituto de Biología Celular y Neurociencia; ArgentinaFil: Cromberg, Lucas Eneas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Biología Celular y Neurociencia "Prof. Eduardo de Robertis". Universidad de Buenos Aires. Facultad de Medicina. Instituto de Biología Celular y Neurociencia; ArgentinaFil: Pozo Devoto, Victorio Martin. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Biología Celular y Neurociencia "Prof. Eduardo de Robertis". Universidad de Buenos Aires. Facultad de Medicina. Instituto de Biología Celular y Neurociencia; ArgentinaFil: Oubiña, Gonzalo. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; ArgentinaFil: Sosa, Lucas Javier. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; ArgentinaFil: Buffone, Mariano Gabriel. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; ArgentinaFil: Gelman, Diego Matias. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; ArgentinaFil: Falzone, Tomas Luis. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Biología Celular y Neurociencia "Prof. Eduardo de Robertis". Universidad de Buenos Aires. Facultad de Medicina. Instituto de Biología Celular y Neurociencia; Argentin
Cosmological parameter estimation using Very Small Array data out to l=1500
We estimate cosmological parameters using data obtained by the Very Small
Array (VSA) in its extended configuration, in conjunction with a variety of
other CMB data and external priors. Within the flat CDM model, we find
that the inclusion of high resolution data from the VSA modifies the limits on
the cosmological parameters as compared to those suggested by WMAP alone, while
still remaining compatible with their estimates. We find that , , , , and
for WMAP and VSA when no external prior is
included.On extending the model to include a running spectral index of density
fluctuations, we find that the inclusion of VSA data leads to a negative
running at a level of more than 95% confidence (),
something which is not significantly changed by the inclusion of a stringent
prior on the Hubble constant. Inclusion of prior information from the 2dF
galaxy redshift survey reduces the significance of the result by constraining
the value of . We discuss the veracity of this result in the
context of various systematic effects and also a broken spectral index model.
We also constrain the fraction of neutrinos and find that at
95% confidence which corresponds to when all neutrino
masses are the equal. Finally, we consider the global best fit within a general
cosmological model with 12 parameters and find consistency with other analyses
available in the literature. The evidence for is only marginal
within this model
Estimating the bispectrum of the Very Small Array data
We estimate the bispectrum of the Very Small Array data from the compact and
extended configuration observations released in December 2002, and compare our
results to those obtained from Gaussian simulations. There is a slight excess
of large bispectrum values for two individual fields, but this does not appear
when the fields are combined. Given our expected level of residual point
sources, we do not expect these to be the source of the discrepancy. Using the
compact configuration data, we put an upper limit of 5400 on the value of f_NL,
the non-linear coupling parameter, at 95 per cent confidence. We test our
bispectrum estimator using non-Gaussian simulations with a known bispectrum,
and recover the input values.Comment: 17 pages, 16 figures, replaced with version accepted by MNRAS.
Primordial bispectrum recalculated and figure 11 change
Comparison of sequencing-based methods to profile DNA methylation and identification of monoallelic epigenetic modifications.
Analysis of DNA methylation patterns relies increasingly on sequencing-based profiling methods. The four most frequently used sequencing-based technologies are the bisulfite-based methods MethylC-seq and reduced representation bisulfite sequencing (RRBS), and the enrichment-based techniques methylated DNA immunoprecipitation sequencing (MeDIP-seq) and methylated DNA binding domain sequencing (MBD-seq). We applied all four methods to biological replicates of human embryonic stem cells to assess their genome-wide CpG coverage, resolution, cost, concordance and the influence of CpG density and genomic context. The methylation levels assessed by the two bisulfite methods were concordant (their difference did not exceed a given threshold) for 82% for CpGs and 99% of the non-CpG cytosines. Using binary methylation calls, the two enrichment methods were 99% concordant and regions assessed by all four methods were 97% concordant. We combined MeDIP-seq with methylation-sensitive restriction enzyme (MRE-seq) sequencing for comprehensive methylome coverage at lower cost. This, along with RNA-seq and ChIP-seq of the ES cells enabled us to detect regions with allele-specific epigenetic states, identifying most known imprinted regions and new loci with monoallelic epigenetic marks and monoallelic expression
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