40,266 research outputs found
On self-protecting singlets in cuprate superconductors
The basal area (Cu-Cu grid) of the cuprate superconductors not only tends to
shrink on hole doping, as expected from single electron quantum chemistry, but
exhibits also an electronically incompressible "hump'' around optimum doping
n_opt = 0.16. The hump collapses near critical doping n_crit = 0.19. We analyze
the origin of the hump in terms of a classical liquid of interacting
incompressible particles in a container with antiferromagnetic walls. Oxygen
holes interacting with the wall form singlets, protect themselves against other
holes by an incompressible "spin fence'', and thus interact also with the
lattice. Occupation of the CuO_2 lattice with holes must therefore follow a
non-double-occupant constraint also for the oxygen cage enclosing the copper
hole. Closest packing of self-protecting singlets is found to occur around
critical doping; closest packing of paired self-protecting singlets around
optimum doping. These singlet-states are bosonic, but are not magnetic
polarons.Comment: reviewed version, 7 pages, 10 figure
Brownian dynamics simulations of planar mixed flows of polymer solutions at finite concentrations
Periodic boundary conditions for planar mixed flows are implemented in the
context of a multi-chain Brownian dynamics simulation algorithm. The effect of
shear rate , and extension rate , on the size of
polymer chains, \left, and on the polymer contribution to
viscosity, , is examined for solutions of FENE dumbbells at finite
concentrations, with excluded volume interactions between the beads taken into
account. The influence of the mixedness parameter, , and flow strength,
, on \left and , is also examined, where
corresponds to pure shear flow, and
corresponds to pure extensional flow. It is shown that there exists a critical
value, , such that the flow is shear dominated for , and extension dominated for .Comment: 18 pages, 12 figures, to appear in Chemical Engineering Scienc
Sensing viruses by mechanical tension of DNA in responsive hydrogels
The rapid worldwide spread of severe viral infections, often involving novel
modifications of viruses, poses major challenges to our health care systems.
This means that tools that can efficiently and specifically diagnose viruses
are much needed. To be relevant for a broad application in local health care
centers, such tools should be relatively cheap and easy to use. Here we discuss
the biophysical potential for the macroscopic detection of viruses based on the
induction of a mechanical stress in a bundle of pre-stretched DNA molecules
upon binding of viruses to the DNA. We show that the affinity of the DNA to the
charged virus surface induces a local melting of the double-helix into two
single-stranded DNA. This process effects a mechanical stress along the DNA
chains leading to an overall contraction of the DNA. Our results suggest that
when such DNA bundles are incorporated in a supporting matrix such as a
responsive hydrogel, the presence of viruses may indeed lead to a significant,
macroscopic mechanical deformation of the matrix. We discuss the biophysical
basis for this effect and characterize the physical properties of the
associated DNA melting transition. In particular, we reveal several scaling
relations between the relevant physical parameters of the system. We promote
this DNA-based assay for efficient and specific virus screening.Comment: 11 pages, 7 figures, supplementary material included in the source
file
Gaussian ellipsoid model for confined polymer systems
Polymer systems in slab geometries are studied on the basis of the recently
presented Gaussian Ellipsoid Model [J. Chem. Phys. 114, 7655 (2001)].The
potential of the confining walls has an exponential shape. For homogeneous
systems in thermodynamic equilibrium we discuss density, orientation and
deformation profiles of the polymers close to the walls. For strongly
segregated mixtures of polymer components A and B equilibrium profiles are
studied near a planar interface separating A and B rich regions. Spinodal
decomposition processes of the mixtures in the presence of neutral walls show
upon strong confinement an increase of the lateral size of A and B rich domains
and a slowing down of the demixing kinetics. These findings are in agreement
with predictions from time dependent Ginzburg--Landau theory. In the case,
where one wall periodically favors one of the two mixture components over the
other, different equilibrium structures emerge and lead to different kinetic
pathways of spinodal decomposition processes in such systems.Comment: 18 pages, 16 figures, submitted to J. Chem. Phy
Microfluidic systems for the analysis of the viscoelastic fluid flow phenomena in porous media
In this study, two microfluidic devices are proposed as simplified 1-D microfluidic analogues of a porous medium. The objectives are twofold: firstly to assess the usefulness of the microchannels to mimic the porous medium in a controlled and simplified manner, and secondly to obtain a better insight about the flow characteristics of viscoelastic fluids flowing through a packed bed. For these purposes, flow visualizations and pressure drop measurements are conducted with Newtonian and viscoelastic fluids. The 1-D microfluidic analogues of porous medium consisted of microchannels with a sequence of contractions/ expansions disposed in symmetric and asymmetric arrangements. The real porous medium is in reality, a complex combination of the two arrangements of particles simulated with the microchannels, which can be considered as limiting ideal configurations. The results show that both configurations are able to mimic well the pressure drop variation with flow rate for Newtonian fluids. However, due to the intrinsic differences in the deformation rate profiles associated with each microgeometry, the symmetric configuration is more suitable for studying the flow of viscoelastic fluids at low De values, while the asymmetric configuration provides better results at high De values. In this way, both microgeometries seem to be complementary and could be interesting tools to obtain a better insight about the flow of viscoelastic fluids through a porous medium. Such model systems could be very interesting to use in polymer-flood processes for enhanced oil recovery, for instance, as a tool for selecting the most suitable viscoelastic fluid to be used in a specific formation. The selection of the fluid properties of a detergent for cleaning oil contaminated soil, sand, and in general, any porous material, is another possible application
Confocal and multiphoton imaging of intracellular Ca<sup>2+</sup>
This chapter compares the imaging capabilities of a range of systems including multiphoton microscopy in regard to measurements of intracellular Ca<sup>2+</sup> within living cells. In particular, the excitation spectra of popular fluorescent Ca<sup>2+</sup> indicators are shown during 1P and 2P excitation. The strengths and limitations of the current indicators are discussed along with error analysis which highlights the value of matching the Ca<sup>2+</sup> affinity of the dye to a particular aspect of Ca<sup>2+</sup> signaling. Finally, the combined emission spectra of Ca<sup>2+</sup> and voltage sensitive dyes are compared to allow the choice of the optimum combination to allow simultaneous intracellular Ca<sup>2+</sup> and membrane voltage measurement
Pathologic gene network rewiring implicates PPP1R3A as a central regulator in pressure overload heart failure
Heart failure is a leading cause of mortality, yet our understanding of the genetic interactions underlying this disease remains incomplete. Here, we harvest 1352 healthy and failing human hearts directly from transplant center operating rooms, and obtain genome-wide genotyping and gene expression measurements for a subset of 313. We build failing and non-failing cardiac regulatory gene networks, revealing important regulators and cardiac expression quantitative trait loci (eQTLs). PPP1R3A emerges as a regulator whose network connectivity changes significantly between health and disease. RNA sequencing after PPP1R3A knockdown validates network-based predictions, and highlights metabolic pathway regulation associated with increased cardiomyocyte size and perturbed respiratory metabolism. Mice lacking PPP1R3A are protected against pressure-overload heart failure. We present a global gene interaction map of the human heart failure transition, identify previously unreported cardiac eQTLs, and demonstrate the discovery potential of disease-specific networks through the description of PPP1R3A as a central regulator in heart failure
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