Role of confined phonons in thin film superconductivity

We calculate the critical temperature $T_c$ and the superconducting energy gaps $\Delta_n$ of a thin film superconductor system, where $\Delta_n$ is the superconducting energy gap of the $n$-th subband. Since the quantization of both the electron energy and phonon spectrum arises due to dimensional confinement in one direction, the effective electron-electron interaction mediated by the quantized confined phonons is different from that mediated by the bulk phonon, leading to the modification of $T_c$ in the thin film system. We investigate the dependence of $T_c$ and $\Delta_n$ on the film thickness $d$ with this modified interaction.Comment: 4 pages, 2 figure

Acute- and late-phase matrix metalloproteinase (MMP)-9 activity is comparable in female and male rats after peripheral nerve injury.

BACKGROUND:In the peripheral nerve, pro-inflammatory matrix metalloproteinase (MMP)-9 performs essential functions in the acute response to injury. Whether MMP-9 activity contributes to late-phase injury or whether MMP-9 expression or activity after nerve injury is sexually dimorphic remains unknown. METHODS:Patterns of MMP-9 expression, activity and excretion were assessed in a model of painful peripheral neuropathy, sciatic nerve chronic constriction injury (CCI), in female and male rats. Real-time Taqman RT-PCR for MMP-9 and its endogenous inhibitor, tissue inhibitor of metalloproteinase-1 (TIMP-1) of nerve samples over a 2-month time course of CCI was followed by gelatin zymography of crude nerve extracts and purified MMP-9 from the extracts using gelatin Sepharose-beads. MMP excretion was determined using protease activity assay of urine in female and male rats with CCI. RESULTS:The initial upsurge in nerve MMP-9 expression at day 1 post-CCI was superseded more than 100-fold at day 28 post-CCI. The high level of MMP-9 expression in late-phase nerve injury was accompanied by the reduction in TIMP-1 level. The absence of MMP-9 in the normal nerve and the presence of multiple MMP-9 species (the proenzyme, mature enzyme, homodimers, and heterodimers) was observed at day 1 and day 28 post-CCI. The MMP-9 proenzyme and mature enzyme species dominated in the early- and late-phase nerve injury, consistent with the high and low level of TIMP-1 expression, respectively. The elevated nerve MMP-9 levels corresponded to the elevated urinary MMP excretion post-CCI. All of these findings were comparable in female and male rodents. CONCLUSION:The present study offers the first evidence for the excessive, uninhibited proteolytic MMP-9 activity during late-phase painful peripheral neuropathy and suggests that the pattern of MMP-9 expression, activity, and excretion after peripheral nerve injury is universal in both sexes

The alternatively spliced fibronectin CS1 isoform regulates IL-17A levels and mechanical allodynia after peripheral nerve injury.

BackgroundMechanical pain hypersensitivity associated with physical trauma to peripheral nerve depends on T-helper (Th) cells expressing the algesic cytokine, interleukin (IL)-17A. Fibronectin (FN) isoform alternatively spliced within the IIICS region encoding the 25-residue-long connecting segment 1 (CS1) regulates T cell recruitment to the sites of inflammation. Herein, we analyzed the role of CS1-containing FN (FN-CS1) in IL-17A expression and pain after peripheral nerve damage.MethodsMass spectrometry, immunoblotting, and FN-CS1-specific immunofluorescence analyses were employed to examine FN expression after chronic constriction injury (CCI) in rat sciatic nerves. The acute intra-sciatic nerve injection of the synthetic CS1 peptide (a competitive inhibitor of the FN-CS1/α4 integrin binding) was used to elucidate the functional significance of FN-CS1 in mechanical and thermal pain hypersensitivity and IL-17A expression (by quantitative Taqman RT-PCR) after CCI. The CS1 peptide effects were analyzed in cultured primary Schwann cells, the major source of FN-CS1 in CCI nerves.ResultsFollowing CCI, FN expression in sciatic nerve increased with the dominant FN-CS1 deposition in endothelial cells, Schwann cells, and macrophages. Acute CS1 therapy attenuated mechanical allodynia (pain from innocuous stimulation) but not thermal hyperalgesia and reduced the levels of IL-17A expression in the injured nerve. CS1 peptide inhibited the LPS- or starvation-stimulated activation of the stress ERK/MAPK pathway in cultured Schwann cells.ConclusionsAfter physical trauma to the peripheral nerve, FN-CS1 contributes to mechanical pain hypersensitivity by increasing the number of IL-17A-expressing (presumably, Th17) cells. CS1 peptide therapy can be developed for pharmacological control of neuropathic pain

Giant Strengthening of Superconducting Pairing in Metallic Nanoclusters

The presence of shell structure and the accompanying high level degeneracy leads to a strengthening of the pairing interaction in some metallic nanoclusters and ions. It is predicted that for some specific systems one can expect a large increase in the values of the critical temperature and other parameters

Scaling of the superfluid density in high-temperature superconductors

A scaling relation \rho_s \simeq 35\sigma_{dc}T_c has been observed in the copper-oxide superconductors, where \rho_s is the strength of the superconducting condensate, T_c is the critical temperature, and \sigma_{dc} is the normal-state dc conductivity close to T_c. This scaling relation is examined within the context of a clean and dirty-limit BCS superconductor. These limits are well established for an isotropic BCS gap 2\Delta and a normal-state scattering rate 1/\tau; in the clean limit 1/\tau \ll 2\Delta, and in the dirty limit 1/\tau > 2\Delta. The dirty limit may also be defined operationally as the regime where \rho_s varies with 1/\tau. It is shown that the scaling relation \rho_s \propto \sigma_{dc}T_c is the hallmark of a BCS system in the dirty-limit. While the gap in the copper-oxide superconductors is considered to be d-wave with nodes and a gap maximum \Delta_0, if 1/\tau > 2\Delta_0 then the dirty-limit case is preserved. The scaling relation implies that the copper-oxide superconductors are likely to be in the dirty limit, and that as a result the energy scale associated with the formation of the condensate is scaling linearly with T_c. The a-b planes and the c axis also follow the same scaling relation. It is observed that the scaling behavior for the dirty limit and the Josephson effect (assuming a BCS formalism) are essentially identical, suggesting that in some regime these two effects may be viewed as equivalent. This raises the possibility that electronic inhomogeneities in the copper-oxygen planes may play an important role in the nature of the superconductivity in the copper-oxide materials.Comment: 8 pages with 5 figures and 1 tabl

Immunological predictors of type 1 diabetes mellitus (literature review)

Background: Type 1 diabetes mellitus (T1DM) is a chronic autoimmune disease characterized by insulin deficiency due β-cell destruction and following hyperglycaemia. Specific markers of T1DM are pancreatic islet-targeting autoantibodies that are found months to years before symptom onset, and can be used to identify individuals who are at risk of developing T1DM.Aim: The study is aimed at the review of current knowledge of diabetes-related autoantibodies as biomarkers of T1DM.Materials and methods: Foreign and national clinical studies on this topic were included. PubMed, Medline and ­eLibrary were searched.Results: Modern ideas about known diabetes-specific autoantibodies as markers of autoimmune inflammation of β-cells of the pancreas were discussed. The analysis of their independent diagnostic value in predicting the occurrence of T1DM were carried out.Conclusion: There is no unified concept in the literature on this issue. Current data on autoantibodies in T1DM show a ­significant individual variability in the timing, dynamic changes and autoantibody composition in T1DM progression

Extracting the electron--boson spectral function α2\alpha^2F(ω\omega) from infrared and photoemission data using inverse theory

We present a new method of extracting electron-boson spectral function $\alpha^2$F($\omega$) from infrared and photoemission data. This procedure is based on inverse theory and will be shown to be superior to previous techniques. Numerical implementation of the algorithm is presented in detail and then used to accurately determine the doping and temperature dependence of the spectral function in several families of high-T$_c$ superconductors. Principal limitations of extracting $\alpha^2$F($\omega$) from experimental data will be pointed out. We directly compare the IR and ARPES $\alpha^2$F($\omega$) and discuss the resonance structure in the spectra in terms of existing theoretical models

Parity-Affected Superconductivity in Ultrasmall Metallic Grains

We investigate the breakdown of BCS superconductivity in {\em ultra}\/small metallic grains as a function of particle size (characterized by the mean spacing $d$ between discrete electronic eigenstates), and the parity ($P$ = even/odd) of the number of electrons on the island. Assuming equally spaced levels, we solve the parity-dependent BCS gap equation for the order parameter $\Delta_P (d,T)$. Both the $T=0$ critical level spacing $d_{c,P}$ and the critical temperature $T_{c,P} (d)$ at which $\Delta_P = 0$ are parity dependent, and both are so much smaller in the odd than the even case that these differences should be measurable in current experiments.Comment: 4 pages RevTeX, 1 encapsulated postscript figure, submitted to Physical Review Letter

Universal transport in 2D granular superconductors

The transport properties of quench condensed granular superconductors are presented and analyzed. These systems exhibit transitions from insulating to superconducting behavior as a function of inter-grain spacing. Superconductivity is characterized by broad transitions in which the resistance drops exponentially with reducing temperature. The slope of the log R versus T curves turns out to be universaly dependent on the normal state film resistance for all measured granular systems. It does not depend on the material, critical temperature, geometry, or experimental set-up. We discuss possible physical scenarios to explain these findings.Comment: 4 pages, 3 figure

New Details of HCV NS3/4A Proteinase Functionality Revealed by a High-Throughput Cleavage Assay

Background: The hepatitis C virus (HCV) genome encodes a long polyprotein, which is processed by host cell and viral proteases to the individual structural and non-structural (NS) proteins. HCV NS3/4A serine proteinase (NS3/4A) is a noncovalent heterodimer of the N-terminal,,180-residue portion of the 631-residue NS3 protein with the NS4A co-factor. NS3/ 4A cleaves the polyprotein sequence at four specific regions. NS3/4A is essential for viral replication and has been considered an attractive drug target. Methodology/Principal Findings: Using a novel multiplex cleavage assay and over 2,660 peptide sequences derived from the polyprotein and from introducing mutations into the known NS3/4A cleavage sites, we obtained the first detailed fingerprint of NS3/4A cleavage preferences. Our data identified structural requirements illuminating the importance of both the short-range (P1–P19) and long-range (P6-P5) interactions in defining the NS3/4A substrate cleavage specificity. A newly observed feature of NS3/4A was a high frequency of either Asp or Glu at both P5 and P6 positions in a subset of the most efficient NS3/4A substrates. In turn, aberrations of this negatively charged sequence such as an insertion of a positively charged or hydrophobic residue between the negatively charged residues resulted in inefficient substrates. Because NS5B misincorporates bases at a high rate, HCV constantly mutates as it replicates. Our analysis revealed that mutations do not interfere with polyprotein processing in over 5,000 HCV isolates indicating a pivotal role of NS3/4A proteolysis in the viru