62 research outputs found
Hole Transport in p-Type ZnO
A two-band model involving the A- and B-valence bands was adopted to analyze
the temperature dependent Hall effect measured on N-doped \textit{p}-type ZnO.
The hole transport characteristics (mobilities, and effective Hall factor) are
calculated using the ``relaxation time approximation'' as a function of
temperature. It is shown that the lattice scattering by the acoustic
deformation potential is dominant. In the calculation of the scattering rate
for ionized impurity mechanism, the activation energy of 100 or 170 meV is used
at different compensation ratios between donor and acceptor concentrations. The
theoretical Hall mobility at acceptor concentration of
cm is about 70 cmVs with the activation energy of 100 meV
and the compensation ratio of 0.8 at 300 K. We also found that the compensation
ratios conspicuously affected the Hall mobilities.Comment: 5page, 5 figures, accepted for publication in Jpn. J. Appl. Phy
Optical Properties of ZnO-based Quantum Structures
The optical properties of ZnO quantum wells, which have potential application
of short-wavelength semiconductor laser utilizing a high-density excitonic
effect, were investigated. Stimulated emission of excitons was observed at
temperatures well above room temperature due to the adoption of the
lattice-matched substrates. The mechanism of stimulated emission from ZnO
quantum wells is discussed in this paperComment: 14 pages, 10 figures, proceeding of the Euro-MRS 2005 held in
Strasbourg, to appear in Superlattices and Microstructure
Single crystalline ZnO films grown on lattice-matched ScAlMgO4(0001) substrates
科研費報告書収録論文(課題番号:09355030・基盤研究(A)(2)・H9~H11/研究代表者:宮本, 明/次世代エレクトロニクス材料としての酸化物人口超格子の原子レベル設計と開発
Cloning and Characterization of the Antiviral Activity of Feline Tetherin/BST-2
Human Tetherin/BST-2 has recently been identified as a cellular antiviral factor that blocks the release of various enveloped viruses. In this study, we cloned a cDNA fragment encoding a feline homolog of Tetherin/BST-2 and characterized the protein product. The degree of amino acid sequence identity between human Tetherin/BST-2 and the feline homolog was 44.4%. Similar to human Tetherin/BST-2, the expression of feline Tetherin/BST-2 mRNA was inducible by type I interferon (IFN). Exogenous expression of feline Tetherin/BST-2 efficiently inhibited the release of feline endogenous retrovirus RD-114. The extracellular domain of feline Tetherin/BST-2 has two putative N-linked glycosylation sites, N79 and N119. Complete loss of N-linked glycosylation by introduction of mutations into both sites resulted in almost complete abolition of its antiviral activity. In addition, feline Tetherin/BST-2 was insensitive to antagonism by HIV-1 Vpu, although the antiviral activity of human Tetherin/BST-2 was antagonized by HIV-1 Vpu. Our data suggest that feline Tetherin/BST-2 functions as a part of IFN-induced innate immunity against virus infection and that the induction of feline Tetherin/BST-2 in vivo may be effective as a novel antiviral strategy for viral infection
Recombination dynamics of excitons in Mg0.11Zn0.89O alloy films grown using the high-temperature-annealed self-buffer layer by laser-assisted molecular-beam epitaxy
科研費報告書収録論文(課題番号:18350092/研究代表者:大友明/高効率酸化亜鉛系青色・紫外発光素子の開発
Chronic high-fat feeding impairs adaptive induction of mitochondrial fatty acid combustion-associated proteins in brown adipose tissue of mice
Since brown adipose tissue (BAT) is involved in thermogenesis using fatty acids as a fuel, BAT activation is a potential strategy for treating obesity and diabetes. However, whether BAT fatty acid combusting capacity is preserved in these conditions has remained unclear. We therefore evaluated expression levels of fatty acid oxidation-associated enzymes and uncoupling protein 1 (Ucp1) in BAT by western blot using a diet-induced obesity C57BL/6J mouse model. In C57BL/6J mice fed a high-fat diet (HFD) over 2–4 weeks, carnitine palmitoyltransferase 2 (Cpt2), acyl-CoA thioesterase (Acot) 2, Acot11 and Ucp1 levels were significantly increased compared with baseline and control low-fat diet (LFD)-fed mice. Similar results were obtained in other mouse strains, including ddY, ICR and KK-Ay, but the magnitudes of the increase in Ucp1 level were much smaller than in C57BL/6J mice, with decreased Acot11 levels after HFD-feeding. In C57BL/6J mice, increased levels of these mitochondrial proteins declined to near baseline levels after a longer-term HFD-feeding (20 weeks), concurrent with the accumulation of unilocular, large lipid droplets in brown adipocytes. Extramitochondrial Acot11 and acyl-CoA oxidase remained elevated. Treatment of mice with Wy-14,643 also increased these proteins, but was less effective than 4 week-HFD, suggesting that mechanisms other than peroxisome proliferator-activated receptor α were also involved in the upregulation. These results suggest that BAT enhances its fatty acid combusting capacity in response to fat overload, however profound obesity deprives BAT of the responsiveness to fat, possibly via mitochondrial alteration
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