Pump frequency resonances for light-induced incipient superconductivity in YBa2_2Cu3_3O6.5_{6.5}

Optical excitation in the cuprates has been shown to induce transient superconducting correlations above the thermodynamic transition temperature, $T_C$, as evidenced by the terahertz frequency optical properties in the non-equilibrium state. In YBa$_2$Cu$_3$O$_{6+x}$ this phenomenon has so far been associated with the nonlinear excitation of certain lattice modes and the creation of new crystal structures. In other compounds, like La$_{2-x}$Ba$_x$CuO$_4$, similar effects were reported also for excitation at near infrared frequencies, and were interpreted as a signature of the melting of competing orders. However, to date it has not been possible to systematically tune the pump frequency widely in any one compound, to comprehensively compare the frequency dependent photo-susceptibility for this phenomenon. Here, we make use of a newly developed optical parametric amplifier, which generates widely tunable high intensity femtosecond pulses, to excite YBa$_2$Cu$_3$O$_{6.5}$ throughout the entire optical spectrum (3 - 750 THz). In the far-infrared region (3 - 25 THz), signatures of non-equilibrium superconductivity are induced only for excitation of the 16.4 THz and 19.2 THz vibrational modes that drive $c$-axis apical oxygen atomic positions. For higher driving frequencies (25 - 750 THz), a second resonance is observed around the charge transfer band edge at ~350 THz. These observations highlight the importance of coupling to the electronic structure of the CuO$_2$ planes, either mediated by a phonon or by charge transfer.Comment: 47 pages, 21 figures, 2 table

Dynamical decoherence of the light induced interlayer coupling in YBa2_{2}Cu3_{3}O6+δ_{6+\delta}

Optical excitation of apical oxygen vibrations in YBa$_{2}$Cu$_{3}$O$_{6+\delta}$ has been shown to enhance its c-axis superconducting-phase rigidity, as evidenced by a transient blue shift of the equilibrium inter-bilayer Josephson plasma resonance. Surprisingly, a transient c-axis plasma mode could also be induced above T$_{c}$ by the same apical oxygen excitation, suggesting light activated superfluid tunneling throughout the pseudogap phase of YBa$_{2}$Cu$_{3}$O$_{6+\delta}$. However, despite the similarities between the above T$_{c}$ transient plasma mode and the equilibrium Josephson plasmon, alternative explanations involving high mobility quasiparticle transport should be considered. Here, we report an extensive study of the relaxation of the light-induced plasmon into the equilibrium incoherent phase. These new experiments allow for a critical assessment of the nature of this mode. We determine that the transient plasma relaxes through a collapse of its coherence length rather than its carrier (or superfluid) density. These observations are not easily reconciled with quasiparticle interlayer transport, and rather support transient superfluid tunneling as the origin of the light-induced interlayer coupling in YBa$_{2}$Cu$_{3}$O$_{6+\delta}$.Comment: 27 pages (17 pages main text, 10 pages supplementary), 5 figures (main text

Excitation dependent Fano-like interference effects in plasmonic silver nanorods

Surface plasmon resonances in metal nanoparticles are an emerging technology platform for nano-optics applications from sensing to solar energy conversion. The electromagnetic near field associated with these resonances arises from modes determined by the shape, size, and composition of the metal nanoparticle. When coupled in the near field, multiple resonant modes can interact to give rise to interference effects offering fine control of both the spectral response and spatial distribution of fields near the particle. Here, we present an examination of experimental electron energy loss spectroscopy (EELS) of silver nanorod monomer surface plasmon modes and present an explanation of observed spatial amplitude modulation of the Fabry-Pérot resonance modes of these silver nanorods using electrodynamics simulations. For these simulations, we identify differences in spectral peak symmetry in light scattering and electron spectroscopies (EELS and cathodoluminescence) and analyze the distinct near-field responses of silver nanorods to plane-wave light and electron beam excitation in terms of a coupled oscillator model. Effects of properties of the material and the incident field are evaluated, and the spatially resolved EELS signals are shown to provide a signature for assessing Fano-like interference effects in silver nanorods. These findings outline key considerations and challenges for interpreting electron microscopy data on plasmonic nanoparticles for understanding nanoscale optics and for characterization and design of photonic devices.S.M.C. acknowledges support of a Gates Cambridge Scholarship. D.R. acknowledges support from the Royal Society's Newton International Fellowship scheme. We acknowledge the use of computing facilities provided by CamGrid. Parts of this work were also performed using the Darwin Supercomputer of the University of Cambridge High Performance Computing Service (http://www.hpc.cam.ac.uk/), provided by Dell Inc. using Strategic Research Infrastructure Funding from the Higher Education Funding Council for England and funding from the Science and Technology Facilities Council. We thank F.J. de la Peña for helpful discussions on the use of hyperspy. The research leading to these results has received funding from the European Research Council under the European Union's Seventh Framework Program (Grant No. FP7/2007-2013)/ERC Grant Agreement No. 291522-3DIMAGE. Data on rod “B” were acquired by one of us (D. Rossouw) with support of a NSERC Discovery Grant (G. A. Botton) at the Canadian Centre for Electron Microscopy, a national facility supported by NSERC and McMaster University. We thank G. A. Botton for access to data on rod “B” and for helpful comments on this manuscript. P.A.M. also acknowledges funding from the European Union's Seventh Framework Program under a contract for an Integrated Infrastructure Initiative (Reference No. 312483-ESTEEM2)

Comparisons of halogenated ß-nitrostyrenes as antimicrobial agents

The influence of three types of halogen-substituted E-ß-methyl-ß-nitrostyrenes (such as Compounds B, D, H) to overcome bacterial activity that is currently a significant health threat was studied. The evaluations of their bio-potency was measured and related to their structure and activity relationships for the purposes of serving to inhibit and overcoming resistant microorganisms. In particular, fluorine-containing ß-nitrostyrenes were found to be highly active antimicrobial agents. The addition of the ß-bromo group enhanced the antibacterial activity significantly. Our work has illustrated that halogen substituents at both the 4-position in the aromatic ring and also at the ß-position on the alkene side chain of nitropropenyl arenes enhanced the antimicrobial activity of these compounds

Hyaluronic acid modulates growth, morphology and cytoskeleton in embryonic chick skin fibroblasts

The action that hyaluronic acid (HA) exerts on cell proliferation was investigated in embryonic chick skin fibroblasts at different ages (7-14 days) and in different cell-cycle stages evaluated by flow cytometry (cells maintained with and without serum). Proliferation was estimated by 3H- thymidine incorporation and cell counting. The results demonstrated hyaluronic acid inhibits cell multiplication in all different environmental conditions examined. The inhibitory effect of HA is more evident in 14-day than 7-day old fibroblasts. The ability of HA to modulate 3H-thymidine incorporation did not involve a change in the time required for cells entering the S phase of the replicating cycle, but is due to a smaller number of cells entering in this phase. As the relationships between components of the extracellular matrix (ECM) and the cytoskeleton are known, parallel studies were carried out on some cytoskeleton proteins. Furthermore, by modifying the capacity of cells to adhere to the substrate, HA induced alterations in cell shape and in cytoskeleton components involved in these processes. We may hypothesize that HA, binding specific membrane receptors, affects cell adhesion and morphology inducing less receptivity of fibroblasts to mitogenic stimuli by transmembrane interactions with cytoskeleton

Attualità sulla sicurezza elettrica delle apparecchiature in uso in chirurgia e medicina interventistica

Il tema della sicurezza di utilizzo delle apparecchiature elettromedicali è diventato di grande attualità a causa della vasta diffusione delle stesse nella pratica medica e chirurgica. Questo aspetto è legato alle specifiche costruttive dell’apparecchio utilizzato, alle specifiche normative che devono essere rispettate dai locali adibiti ad uso medico e al corretto utilizzo delle stesse. L’articolo suggerisce un approccio al problema che delinea gli effetti fisiologici e patologici di correnti elettriche sul corpo umano, indicando successivamente le norme vigenti per la sicurezza elettrica delle apparecchiature elettromedicali e degli impianti utilizzati per scopi medici e chirurgici, esaminando infine alcune situazioni cliniche a rischio elettric

Autoradiographic Characterization and Localization of Quisqualate Binding Sites in Rat Brain Using the Antagonist [ 3 H]6-Cyano-7-Nitroquinoxaline-2,3-Dione: Comparison with ( R,S )-[ 3 H]Α-Amino-3-Hydroxy-5-Methyl-4-Isoxazolepropionic Acid Binding Sites

Using quantitative autoradiography, we have investigated the binding sites for the potent competitive non- N -methyl-D-aspartate (non-NMDA) glutamate receptor antagonist [ 3 H]6-cyano-7-nitro-quinoxaline-2,3-dione ([ 3 H]-CNQX) in rat brain sections. [ 3 H]CNQX binding was regionally distributed, with the highest levels of binding present in hippocampus in the stratum radiatum of CA1, stratum lucidum of CA3, and molecular layer of dentate gyrus. Scatchard analysis of [ 3 H]CNQX binding in the cerebellar molecular layer revealed an apparent single binding site with a K D = 67 ± 9.0 n M and B max = 3.56 ± 0.34 pmol/mg protein. In displacement studies, quisqualate, L-glutamate, and kainate also appeared to bind to a single class of sites. However, ( R,S )- Α -amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) displacement of [ 3 H]CNQX binding revealed two binding sites in the cerebellar molecular layer. Binding of [ 3 H]AMPA to quisqualate receptors in the presence of potassium thiocyanate produced curvilinear Scatchard plots. The curves could be resolved into two binding sites with K D1 = 9.0 ± 3.5 n M , B max = 0.15 ± 0.05 pmol/mg protein, K D2 = 278 ± 50 n M , and B max = 1.54 ± 0.20 pmol/mg protein. The heterogeneous anatomical distribution of [ 3 H]CNQX binding sites correlated to the binding of L-[ 3 H]glutamate to quisqualate receptors and to sites labeled with [ 3 H]AMPA. These results suggest that the non-NMDA glutamate receptor antagonist [ 3 H]CNQX binds with equal affinity to two states of quisqualate receptors which have different affinities for the agonist [ 3 H]AMPA.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/65634/1/j.1471-4159.1990.tb01925.x.pd

A Missense Variant in PTPN22 is a Risk Factor for Drug-induced Liver Injury

BACKGROUND & AIMS: We performed genetic analyses of a multiethnic cohort of patients with idiosyncratic drug-induced liver injury (DILI) to identify variants associated with susceptibility. METHODS: We performed a genome-wide association study of 2048 individuals with DILI (cases) and 12,429 individuals without (controls). Our analysis included subjects of European (1806 cases and 10,397 controls), African American (133 cases and 1,314 controls), and Hispanic (109 cases and 718 controls) ancestry. We analyzed DNA from 113 Icelandic cases and 239,304 controls to validate our findings. RESULTS: We associated idiosyncratic DILI with rs2476601, a nonsynonymous polymorphism that encodes a substitution of tryptophan with arginine in the protein tyrosine phosphatase, nonreceptor type 22 gene (PTPN22) (odds ratio [OR] 1.44; 95% confidence interval [CI] 1.28-1.62; P = 1.2 x 10(-9) and replicated the finding in the validation set (OR 1.48; 95% CI 1.09-1.99; P =.01). The minor allele frequency showed the same effect size (OR > 1) among ethnic groups. The strongest association was with amoxicillin and clavulanate-associated DILI in persons of European ancestry (OR 1.62; 95% CI 1.32-1.98; P = 4.0 x 10(-6); allele frequency = 13.3%), but the polymorphism was associated with DILI of other causes (OR 1.37; 95% CI 1.21-1.56; P = 1.5 x 10(-6); allele frequency = 11.5%). Among amoxicillin-and clavulanate-associated cases of European ancestry, rs2476601 doubled the risk for DILI among those with the HLA risk alleles A* 02: 01 and DRB1* 15: 01. CONCLUSIONS: In a genome-wide association study, we identified rs2476601 in PTPN22 as a non-HLA variant that associates with risk of liver injury caused by multiple drugs and validated our finding in a separate cohort. This variant has been associated with increased risk of autoimmune diseases, providing support for the concept that alterations in immune regulation contribute to idiosyncratic DILI.Peer reviewe

Evaluation of site-specific methylation of the CMV promoter and its role in CHO cell productivity of a recombinant monoclonal antibody

We previously demonstrated that increased monoclonal antibody productivity in dihydrofolate reductase (DHFR)-amplified CHO cells correlates with phosphorylated transcription factor-cytomegalovirus (CMV) promoter interactions. In this article, we extend the characterization to include CMV promoter methylation and its influence on NFκB and CREB1 transcription factor binding to the CMV promoter in two families of DHFR-amplified CHO cell lines. CMV promoter methylation was determined using bisulfite sequencing. To overcome Sanger-sequencing limitations due to high CG bias and multiple transgenes copies, pyrosequencing was used to determine the frequency of methylated cytosines in regions proximal to and containing the NFκB and CREB1 transcription-factor consensus binding sites. Chromatin immunoprecipitation was performed to interrogate transcription factor-DNA interactions. Antibodies to CREB1 and NFκB were used to immunoprecipitate formaldehyde-crosslinked protein-DNA fractions, followed by reverse transcription quantitative real-time polymerase chain reaction to quantitate the number of copies of CMV-promoter DNA bound to the various transcription factors. The relative unmethylated fraction at the CREB1 and NFκB consensus binding sites determined by pyrosequencing was correlated with transcription factor binding as determined by chromatin immunoprecipitation. Azacytidine treatment reduced methylation in all treated samples, though not at all methylation sites, while increasing transcription. Distinct promoter methylation patterns arise upon clonal selection in different families of cell lines. In both cell line families, increased methylation was observed upon amplification. In one family, the NFκB binding-site methylation was accompanied by increased CREB1 interaction with the promoter. In the other cell line family, lower methylation frequency at the NFκB consensus binding site was accompanied by more NFκB recruitment to the promoter region