824 research outputs found
Electron spin resonance shifts in S=1 antiferromagnetic chains
We discuss electron spin resonance (ESR) shifts in spin-1 Heisenberg
antiferromagnetic chains with a weak single-ion anisotropy based on several
effective field theories, the O(3) nonlinear sigma model (NLSM) in the Haldane
phase, free fermion theories around the lower and the upper critical fields. In
the O(3) NLSM, the single-ion anisotropy corresponds to a composite operator
which creates two magnons at the same time and position. Therefore, even inside
a parameter range where free magnon approximation is valid, we have to take
interactions among magnons into account. Though the O(3) NLSM is only valid in
the Haldane phase, an appropriate translation of Faddeev-Zamolodchikov
operators of the O(3) NLSM to fermion operators enables one to treat ESR shifts
near the lower critical field in a similar manner to discussions in Haldane
phase. We present that our theory gives quantitative agreements with recent ESR
experimental results on an spin-1 chain compounds NDMAP
Universal temperature dependence of the magnetization of gapped spin chains
Temperature dependence of the magnetization of the Haldane spin chain at
finite magnetic field is analyzed systematically. Quantum Monte Carlo data
indicates a clear minimum of magnetization as a function of temperature in the
gapless regime. On the basis of the Tomonaga-Luttinger liquid theory, we argue
that this minimum is rather universal and can be observed for general axially
symmetric quasi-one-dimensional spin systems. Our argument is confirmed by the
magnetic-field dependence of the spin-wave velocity obtained numerically. One
can estimate a magnitude of the gap of any such systems by fitting the
experimental data with the magnetization minimum.Comment: 9 pages, 7 figure
Exact Analysis of ESR Shift in the Spin-1/2 Heisenberg Antiferromagnetic Chain
A systematic perturbation theory is developed for the ESR shift and is
applied to the spin-1/2 Heisenberg chain. Using the Bethe ansatz technique, we
exactly analyze the resonance shift in the first order of perturbative
expansion with respect to an anisotropic exchange interaction. Exact result for
the whole range of temperature and magnetic field, as well as asymptotic
behavior in the low-temperature limit are presented. The obtained g-shift
strongly depends on magnetic fields at low temperature, showing a significant
deviation from the previous classical result.Comment: 4 pages, 3 figures,to be published in Phys. Rev. Let
Effects of Z-Isomerization on the Bioavailability and Functionality of Carotenoids: A Review
Carotenoids, the most common fat-soluble plant pigments in nature, are beneficial to human health due to their strong antioxidant activities and abilities to prevent various diseases. Carotenoids have many geometrical isomers forms caused by E/Z-isomerization at arbitrary sites within the multiple conjugated double bonds. Several studies have addressed that the bioavailability as well as the antioxidant, anticancer, and antiatherosclerotic activities of carotenoids varies among the isomers. In addition, those variations differ among carotenoids: Z-isomerization resulted in “positive” or “negative” effect for carotenoids bioavailability and functionality, for example, Z-isomers of lycopene are more bioavailable than the all-E-isomer, whereas the opposite is observed for β-carotene. Thus, to efficiently promote the beneficial effects of carotenoids by ingestion, it is important to have a good understanding of the impact of E/Z-isomerization on the corresponding functional changes. The objective of this contribution is to review the effects of carotenoid Z-isomerization on bioavailability and functionality and describe their differences among carotenoids
Selectively Expanded of CD4+ T Cells from Peripheral Blood Mononuclear Cells Induced by Interleukin-2 Plus Anti-CD3 : Effects on the Cytotoxicity, the Proliferation and the Modulation of HLA Antigens and Intercellular Adhesion Molecule-1 against Human Malignant Melanoma Cell Lines
We selected human CD4? T cells using immunomagnetic beads from periph-eral blood mononuclear cells of 5 healthy volunteers, and cultured with recom-binant interleukin-2 (RIL-2) plus anti-CD3 culture supernatants. After success-ful generation of the CD4? T cell cultures, we examined the therapeutic value for human malignant melanoma. Through flow cytometry analysis, ??Cr-release assay and proliferation assay, we found that a) the total increase in 7 to 10 day cultures ranged from 30 to 100-fold ; b) the expanded cells were mostly CD2?, CD3?, CD4?, CD8?, CD25?, CD29?, CD56? and T cell receptor (α/β)? T cell ; c) some of them possessed moderate levels of natural killer cell and lymphokine -activated killer cell activities ; d) culture supernatants significantly inhibited the growth of cultured human melanoma cell lines ; e) culture supernatants enhanced surface expression of class I, class II and intercellular adhesion molecule-1 on cultured human melanoma cell lines ; and f) culture supernatants contained large amounts of cytokines such as IL-2, IL-6 and interferon-γ. These results sug-gested that selectively expanded CD4+ T cells may be available as a new strategy in the future human adoptive immunotherapy
Bovine Insulin Filaments Induced by Reducing Disulfide Bonds Show a Different Morphology, Secondary Structure, and Cell Toxicity from Intact Insulin Amyloid Fibrils
AbstractAmyloid fibrils are associated with more than 20 diseases, including Alzheimer's disease and type II diabetes. Insulin is a 51-residue polypeptide hormone, with its two polypeptide chains linked by one intrachain and two interchain disulfide bonds, and has long been known to self-assemble in vitro into amyloid fibrils. We demonstrate here that bovine insulin forms flexible filaments in the presence of a reducing agent, Tris (2-carboxyethyl) phosphine. The insulin filaments, possibly formed due to partial reduction of S-S bonds in insulin molecules, differ from intact insulin fibrils in terms of their secondary structure. The insulin filaments were determined to have an antiparallel β-sheet structure, whereas the insulin fibrils have a parallel β-sheet structure. Of importance, the cell toxicity of the insulin filaments was remarkably lower than that of the insulin fibrils. This finding supports the idea that cell toxicity of amyloids correlates with their morphology. The remarkably low toxicity of the filamentous structure should shed new light on possible pharmacological approaches to the various diseases caused by amyloid fibrils
Single-ion anisotropy in Haldane chains and form factor of the O(3) nonlinear sigma model
We consider spin-1 Haldane chains with single-ion anisotropy, which exists in
known Haldane chain materials. We develop a perturbation theory in terms of
anisotropy, where magnon-magnon interaction is important even in the low
temperature limit. The exact two-particle form factor in the O(3) nonlinear
sigma model leads to quantitative predictions on several dynamical properties
including dynamical structure factor and electron spin resonance frequency
shift. These agree very well with numerical results, and with experimental data
on the Haldane chain material Ni(CHN)N(PF)
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