1,563 research outputs found

    Growth, Structural and Micro hardness studies of KSbF4 and K2SbF5 crystals

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    Interest in Potassium Fluoro Antimonate crystals has been increased for the last four decades due its superionic conduction and its unusual electro-optic properties. Potassium tetra fluoro antimonate (KSbF4) and Potassium penta fluoro antimonite (K2SbF5) crystals have been grown by slow evaporation method. KSbF4 crystallizes into orthorhombic structure with a space group Pmmn. K2SbF5 belongs to orthorhombic crystal system with a space group Cmcm.nbsp Micro indentation analysis on these crystals indicates that they are moderately softer substances. Both crystals revealed reverse indentation size effect (RISE). Variation of stiffness constant with load has been discussed. Yield strength for KSbF4 and K2SbF5 crystals have been found out as 16.72 and 16.941 MPa respectively.nbs

    Intrinsic Energy Localization through Discrete Gap Breathers in One-Dimensional Diatomic Granular Crystals

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    We present a systematic study of the existence and stability of discrete breathers that are spatially localized in the bulk of a one-dimensional chain of compressed elastic beads that interact via Hertzian contact. The chain is diatomic, consisting of a periodic arrangement of heavy and light spherical particles. We examine two families of discrete gap breathers: (1) an unstable discrete gap breather that is centered on a heavy particle and characterized by a symmetric spatial energy profile and (2) a potentially stable discrete gap breather that is centered on a light particle and is characterized by an asymmetric spatial energy profile. We investigate their existence, structure, and stability throughout the band gap of the linear spectrum and classify them into four regimes: a regime near the lower optical band edge of the linear spectrum, a moderately discrete regime, a strongly discrete regime that lies deep within the band gap of the linearized version of the system, and a regime near the upper acoustic band edge. We contrast discrete breathers in anharmonic FPU-type diatomic chains with those in diatomic granular crystals, which have a tensionless interaction potential between adjacent particles, and highlight in that the asymmetric nature of the latter interaction potential may lead to a form of hybrid bulk-surface localized solutions

    M.leprae binds to a 28-30 kDa phosphorylated glycoprotein of rat peripheral nerve

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    Understanding the mechanisms of IGF2 gene regulation in hepatocellular carcinoma cells

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    Hepatocellular carcinoma (HCC) is a leading cause of cancer-related deaths worldwide. HCC has a very well studied etiology, and is associated with chronic hepatic viral infections (hepatitis viruses B and C), alcohol abuse, or other causes of chronic liver damage. Currently, tumor resection and liver transplantation are the only potentially curative treatments available for HCC. However, the presence of extra-hepatic invasion and metastasis makes patients ineligible for these treatments. High IGF2 levels are associated with metastatic HCC, and we recently showed that IGF2-induced signaling through Igf1R stimulates the invasiveness and metastatic phenotype of HCC cells. However, the precise mechanisms by which IGF2 expression is enhanced in HCC are not well understood. IGF2 is an imprinted gene normally expressed from the paternal allele. Loss of imprinting, which activates the normally silent maternal allele, has been implicated as an epigenetic marker for the enhanced risk of human cancer. However, many HCCs that display elevated IGF2 expression levels retain a normal imprinting pattern. Therefore, additional gene regulation mechanisms must also influence IGF2 expression in HCC. Hypothesis: Long-range genomic interactions are important for the regulation of IGF2 gene expression, and alterations in these long-range interactions lead to elevated IGF2 gene expression in HCC. To address this hypothesis I have utilized chromosome conformation capture carbon copy (5C) technology to elucidate long-range interactions involving the IGF2 promoters in a normal hepatocyte cell line, THLE-2, and an HCC cell line HepG2

    Loss of a single N-linked glycan from the hemagglutinin of influenza virus is associated with resistance to collectins and increased virulence in mice

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    BACKGROUND: Glycosylation on the globular head of the hemagglutinin (HA) protein of influenza virus acts as an important target for recognition and destruction of virus by innate immune proteins of the collectin family. This, in turn, modulates the virulence of different viruses for mice. The role of particular oligosaccharide attachments on the HA in determining sensitivity to collectins has yet to be fully elucidated. METHODS: When comparing the virulence of H3N2 subtype viruses for mice we found that viruses isolated after 1980 were highly glycosylated and induced mild disease in mice. During these studies, we were surprised to find a small plaque variant of strain A/Beijing/353/89 (Beij/89) emerged following infection of mice and grew to high titres in mouse lung. In the current study we have characterized the properties of this small plaque mutant both in vitro and in vivo. RESULTS: Small plaque mutants were recovered following plaquing of lung homogenates from mice infected with influenza virus seed Beij/89. Compared to wild-type virus, small plaque mutants showed increased virulence in mice yet did not differ in their ability to infect or replicate in airway epithelial cells in vitro. Instead, small plaque variants were markedly resistant to neutralization by murine collectins, a property that correlated with the acquisition of an amino acid substitution at residue 246 on the viral HA. We present evidence that this substitution was associated with the loss of an oligosaccharide glycan from the globular head of HA. CONCLUSION: A point mutation in the gene encoding the HA of Beij/89 was shown to ablate a glycan attachment site. This was associated with resistance to collectins and increased virulence in mice

    Isolation and Characterization of Biotin Carboxylase from Pea Chloroplasts

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