576 research outputs found
Role of critical spin fluctuations in ultrafast demagnetization of transition-metal rare-earth alloys
Ultrafast magnetization dynamics induced by femtosecond laser pulses have
been measured in ferrimagnetic Co0.8Gd0.2, Co.74Tb.26 and Co.86Tb.14 alloys.
Using element sensitivity of X-ray magnetic circular dichroism at the Co L3, Tb
M5 and Gd M5 edges we evidence that the demagnetization dynamics is element
dependent. We show that a thermalization time as fast as 280 fs is observed for
the rare-earth in the alloy, when the laser excited state temperature is below
the compensation temperature. It is limited to 500 fs when the laser excited
state temperature is below the Curie temperature (Tc). We propose critical spin
fluctuations in the vicinity of TC as the mechanism which reduces the
demagnetization rates of the 4f electrons in transition-metal rare-earth alloys
whereas at any different temperature the limited demagnetization rates could be
avoided.Comment: 11 pages, 4 figure
Projet sucrier guyanais. Etude exploratoire dans le but d'identifier le site le plus favorable à la culture de la canne à sucre dans l'Ouest guyanais. Rapport définitif
The MEF2A and MEF2D isoforms are differentially regulated in muscle and adipose tissue during states of insulin deficiency
Previously we have demonstrated that striated muscle GLUT4 gene expression decreased following streptozotocin-induced diabetes due to a loss of MEF2A transcription factor expression without any significant effect on the MEF2D isoform (Mora, S. and J. E. Pessin (2000) J Biol Chem, 275:16323-16328). In contrast to both cardiac and skeletal muscle, adipose tissue displays a selective decrease in MEF2D expression in diabetes without any significant alteration in MEF2A protein content. Adipose tissue also expresses very low levels of the MEF2 transcription factors and nuclear extracts from white adipose tissue exhibit poor in vitro binding to the MEF2 element. However, addition of in vitro synthesized MEF2A to adipose nuclear extracts results in the formation of the expected MEF2/DNA complex. More importantly, binding to the MEF2 element was also compromised in the diabetic condition. Furthermore, in vivo overexpression of MEF2A selectively in adipose tissue did not affect GLUT4 or MEF2D expression and was not sufficient to prevent GLUT4 down-regulation that occurred in insulin-deficient states
Crystal structure of a lipoxygenase in complex with substrate: The arachidonic acid-binding site of 8R-lipoxygenase
Lipoxygenases (LOX) play critical roles in mammalian biology in the generation of potent lipid mediators of the inflammatory response; consequently, they are targets for the development of isoform-specific inhibitors. The regio- and stereo-specificity of the oxygenation of polyunsaturated fatty acids by the enzymes is understood in terms of the chemistry, but structural observation of the enzyme-substrate interactions is lacking. Although several LOX crystal structures are available, heretofore the rapid oxygenation of bound substrate has precluded capture of the enzyme-substrate complex, leaving a gap between chemical and structural insights. In this report, we describe the 2.0 Å resolution structure of 8R-LOX in complex with arachidonic acid obtained under anaerobic conditions. Subtle rearrangements, primarily in the side chains of three amino acids, allow binding of arachidonic acid in a catalytically competent conformation. Accompanying experimental work supports a model in which both substrate tethering and cavity depth contribute to positioning the appropriate carbon at the catalytic machinery
The precise structures and stereochemistry of trihydroxy-linoleates esterified in human and porcine epidermis and their significance in skin barrier function: Implication of an epoxide hydrolase in the transformations of linoleate
Creation of an intact skin water barrier, a prerequisite for life on dry land, requires the lipoxygenase-catalyzed oxidation of the essential fatty acid linoleate, which is esterified to the ω-hydroxyl of an epidermis-specific ceramide. Oxidation of the linoleate moiety by lipoxygenases is proposed to facilitate enzymatic cleavage of the ester bond, releasing free ω-hydroxyceramide for covalent binding to protein, thus forming the corneocyte lipid envelope, a key component of the epidermal barrier. Herein, we report the transformations of esterified linoleate proceed beyond the initial steps of oxidation and epoxyalcohol synthesis catalyzed by the consecutive actions of 12R-LOX and epidermal LOX3. The major end product in human and porcine epidermis is a trihydroxy derivative, formed with a specificity that implicates participation of an epoxide hydrolase in converting epoxyalcohol to triol. Of the 16 possible triols arising from hydrolysis of 9,10-epoxy-13-hydroxy-octadecenoates, using LC-MS and chiral analyses, we identify and quantify specifically 9R,10S,13R-trihydroxy-11E-octadecenoate as the single major triol esterified in porcine epidermis and the same isomer with lesser amounts of its 10R diastereomer in human epidermis. The 9R,10S,13R-triol is formed by SN2 hydrolysis of the 9R,10R-epoxy-13R-hydroxy-octadecenoate product of the LOX enzymes, a reaction specificity characteristic of epoxide hydrolase. The high polarity of triol over the primary linoleate products enhances the concept that the oxidations disrupt corneocyte membrane lipids, promoting release of free ω-hydroxyceramide for covalent binding to protein and sealing of the waterproof barrier
Element resolved ultrafast demagnetization rates in ferrimagnetic CoDy
Femtosecond laser induced ultrafast magnetization dynamics have been studied
in multisublattice CoxDy1-x alloys. By performing element and time-resolved
X-ray spectroscopy, we distinguish the ultrafast quenching of Co3d and Dy4f
magnetic order when the initial temperatures are below (T=150K) or above
(T=270K) the temperature of magnetic compensation (Tcomp). In accordance with
former element-resolved investigations and theoretical calculations, we observe
different dynamics for Co3d and Dy4f spins. In addition we observe that, for a
given laser fluence, the demagnetization amplitudes and demagnetization times
are not affected by the existence of a temperature of magnetic compensation.
However, our experiment reveals a twofold increase of the ultrafast
demagnetization rates for the Dy sublattice at low temperature. In parallel, we
measure a constant demagnetization rate of the Co3d sublattice above and below
Tcomp. This intriguing difference between the Dy4f and Co3d sublattices calls
for further theoretical and experimental investigations.Comment: 6 Figure, 2 Table
The structure of human 5-lipoxygenase
The synthesis of both proinflammatory leukotrienes and anti-inflammatory lipoxins requires the enzyme 5-lipoxygenase (5-LOX). 5-LOX activity is short-lived, apparently in part because of an intrinsic instability of the enzyme. We identified a 5-LOX-specific destabilizing sequence that is involved in orienting the carboxyl terminus, which binds the catalytic iron. Here, we report the crystal structure at 2.4 angstrom resolution of human 5-LOX stabilized by replacement of this sequence
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