97 research outputs found
Electrical and magnetic properties of the complete solid solution series between SrRuO3 and LaRhO3: Filling t2g versus tilting
A complete solid solution series between the t2g^4 perovskite ferromagnet
SrRuO3 and the diamagnetic t2g^6 perovskite LaRhO3 has been prepared. The
evolution with composition x in (SrRuO3)(1-x)(LaRhO3)(x) of the crystal
structure and electrical and magnetic properties has been studied and is
reported here. As x increases, the octahedral tilt angle gradually increases,
along with the pseudocubic lattice parameter and unit cell volume. Electrical
resistivity measurements reveal a compositionally driven metal to insulator
transition between x = 0.1 and 0.2. Ferromagnetic ordering gives over to glassy
magnetism for x > 0.3 and no magnetic ordering is found above 2 K for x > 0.5.
M_sat and Theta_CW decrease with increasing x and remain constant after x =
0.5. The magnetism appears poised between localized and itinerant behavior, and
becomes more localized with increasing x as evidenced by the evolution of the
Rhodes-Wohlfarth ratio. mu_eff per Ru is equal to the quenched spin-only S
value across the entire solid solution. Comparisons with Sr(1-x)Ca(x)RuO3
reinforce the important role of structural distortions in determining magnetic
ground state. It is suggested that electrical transport and magnetic properties
are not strongly coupled in this system
Structural disorder, magnetism, and electrical and thermoelectric properties of pyrochlore Nd2Ru2O7
Polycrystalline Nd2Ru2O7 samples have been prepared and examined using a
combination of structural, magnetic, and electrical and thermal transport
studies. Analysis of synchrotron X-ray and neutron diffraction patterns
suggests some site disorder on the A-site in the pyrochlore sublattice: Ru
substitutes on the Nd-site up to 7.0(3)%, regardless of the different
preparative conditions explored. Intrinsic magnetic and electrical transport
properties have been measured. Ru 4d spins order antiferromagnetically at 143 K
as seen both in susceptibility and specific heat, and there is a corresponding
change in the electrical resistivity behaviour. A second antiferromagnetic
ordering transition seen below 10 K is attributed to ordering of Nd 4f spins.
Nd2Ru2O7 is an electrical insulator, and this behaviour is believed to be
independent of the Ru-antisite disorder on the Nd site. The electrical
properties of Nd2Ru2O7 are presented in the light of data published on all
A2Ru2O7 pyrochlores, and we emphasize the special structural role that Bi3+
ions on the A-site play in driving metallic behaviour. High-temperature
thermoelectric properties have also been measured. When considered in the
context of known thermoelectric materials with useful figures-of-merit, it is
clear that Nd2Ru2O7 has excessively high electrical resistivity which prevents
it from being an effective thermoelectric. A method for screening candidate
thermoelectrics is suggested.Comment: 19 pages, 10 figure
Structural and magnetic characterization of the complete delafossite solid solution (CuAlO2){1-x}(CuCrO2){x}
We have prepared the complete delafossite solid solution series between
diamagnetic CuAlO2 and the t2g^3 frustrated antiferromagnet CuCrO2. The
evolution with composition x in CuAl(1-x)Cr(x)O2 of the crystal structure and
magnetic properties has been studied and is reported here. The room-temperature
unit cell parameters follow the Vegard law and increase with x as expected. The
effective moment is equal to the Cr^3+ spin-only S = 3/2 value throughout the
entire solid solution. Theta is negative, indicating that the dominant
interactions are antiferromagnetic, and its magnitude increases with Cr
substitution. For dilute Cr compositions, J_BB was estimated by mean-field
theory to be 2.0 meV. Despite the sizable Theta, long-range antiferromagnetic
order does not develop until very large x, and is preceeded by glassy behavior.
Data presented here, and that on dilute Al-substitution from Okuda et al.,
suggest that the reduction in magnetic frustration due to the presence of
non-magnetic Al does not have as dominant an effect on magnetism as chemical
disorder and dilution of the magnetic exchange. For all samples, the 5 K
isothermal magnetization does not saturate in fields up to 5 T and minimal
hysteresis is observed. The presence of antiferromagnetic interactions is
clearly evident in the sub-Brillouin behavior with a reduced magnetization per
Cr atom. An inspection of the scaled Curie plot reveals that significant
short-range antiferromagnetic interactions occur in CuCrO2 above its Neel
temperature, consistent with its magnetic frustration. Uncompensated
short-range interactions are present in the Al-substituted samples and are
likely a result of chemical disorder
Electrochemistry of the [4Fe4S] Cluster in Base Excision Repair Proteins: Tuning the Redox Potential with DNA
Escherichia coli endonuclease III (EndoIII) and MutY are DNA glycosylases that contain [4Fe4S] clusters and that serve to maintain the integrity of the genome after oxidative stress. Electrochemical studies on highly oriented pyrolytic graphite (HOPG) revealed that DNA binding by EndoIII leads to a large negative shift in the midpoint potential of the cluster, consistent with stabilization of the oxidized [4Fe4S]^(3+) form. However, the smooth, hydrophobic HOPG surface is nonideal for working with proteins in the absence of DNA. In this work, we use thin film voltammetry on a pyrolytic graphite edge electrode to overcome these limitations. Improved adsorption leads to substantial signals for both EndoIII and MutY in the absence of DNA, and a large negative potential shift is retained with DNA present. In contrast, the EndoIII mutants E200K, Y205H, and K208E, which provide electrostatic perturbations in the vicinity of the cluster, all show DNA-free potentials within error of wild type; similarly, the presence of negatively charged poly-L-glutamate does not lead to a significant potential shift. Overall, binding to the DNA polyanion is the dominant effect in tuning the redox potential of the [4Fe4S] cluster, helping to explain why all DNA-binding proteins with [4Fe4S] clusters studied to date have similar DNA-bound potentials
Caspase 8 and maspin are downregulated in breast cancer cells due to CpG site promoter methylation
<p>Abstract</p> <p>Background</p> <p>Epigenetic changes associated with promoter DNA methylation results in silencing of several tumor suppressor genes that lead to increased risk for tumor formation and for progression of the cancer.</p> <p>Methods</p> <p>Methylation specific PCR (MSP) and bisulfite sequencing were used for determination of proapoptotic gene Caspase 8 (CASP8) and the tumor suppressor gene maspin promoter methylation in four breast cancer and two non-tumorigenic breast cell lines. Involvement of histone H3 methylation in those cell lines were examined by CHIP assay.</p> <p>Results</p> <p>The CpG sites in the promoter region of CASP8 and maspin were methylated in all four breast cancer cell lines but not in two non-tumorigenic breast cell lines. Demethylation agent 5-aza-2'-deoxycytidine (5-aza-dc) selectively inhibits DNA methyltransferases, DNMT3a and DNMT3b, and restored CASP8 and maspin gene expression in breast cancer cells. 5-aza-dc also reduced histone H3k9me2 occupancy on CASP8 promoter in SKBR3cells, but not in MCF-7 cells. Combination of histone deacetylase inhibitor Trichostatin A (TSA) and 5-aza-dc significant decrease in nuclear expression of Di-methyl histone H3-Lys27 and slight increase in acetyl histone H3-Lys9 in MCF-7 cells. CASP8 mRNA and protein level in MCF-7 cells were increased by the 5-aza-dc in combination with TSA. Data from our study also demonstrated that treatment with 5-FU caused a significant increase in unmethylated CASP8 and in CASP8 mRNA in all 3 cancer lines.</p> <p>Conclusions</p> <p>CASP8 and maspin expression were reduced in breast cancer cells due to promoter methylation. Selective application of demethylating agents could offer novel therapeutic opportunities in breast cancer.</p
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