543 research outputs found

    X-Ray Microanalysis of Calcium Containing Organelles in Resin Embedded Tissue

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    The localization of calcium in cell organelles at the electron microscope level is often achieved through cytochemical techniques, and verified by X-ray microanalysis. Various methods have been used to cytochemically detect calcium or calcium-binding sites : calcium loading, calcium substitution by strontium, barium, or even lead, and calcium precipitation by oxalate, phosphate, fluoride, or pyroantimonate. Their results may have heuristic value, particularly in preliminary studies of poorly known cell types. A complementary and more physiological approach is offered by quantitative measurement of the total calcium content of organelles after cryofixation. Resin embedding is less demanding than cryomicrotomy and gives better images : it can be used after cryosubstitution in the presence of oxalic acid. This technique was tested, and applied to several cell types

    Motivic Serre invariants, ramification, and the analytic Milnor fiber

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    We show how formal and rigid geometry can be used in the theory of complex singularities, and in particular in the study of the Milnor fibration and the motivic zeta function. We introduce the so-called analytic Milnor fiber associated to the germ of a morphism f from a smooth complex algebraic variety X to the affine line. This analytic Milnor fiber is a smooth rigid variety over the field of Laurent series C((t)). Its etale cohomology coincides with the singular cohomology of the classical topological Milnor fiber of f; the monodromy transformation is given by the Galois action. Moreover, the points on the analytic Milnor fiber are closely related to the motivic zeta function of f, and the arc space of X. We show how the motivic zeta function can be recovered as some kind of Weil zeta function of the formal completion of X along the special fiber of f, and we establish a corresponding Grothendieck trace formula, which relates, in particular, the rational points on the analytic Milnor fiber over finite extensions of C((t)), to the Galois action on its etale cohomology. The general observation is that the arithmetic properties of the analytic Milnor fiber reflect the structure of the singularity of the germ f.Comment: Some minor errors corrected. The original publication is available at http://www.springerlink.co

    Focal autoimmune pancreatitis

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    A 70-year-old man was referred for evaluation of mild epigastric discomfort with tiredness. He had no particular medical history and admitted drinking two glasses of wine a day. Biology showed a small increase in CRP and pancreatic enzymes (lipases and amylases)

    Well-Posedness and Symmetries of Strongly Coupled Network Equations

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    We consider a diffusion process on the edges of a finite network and allow for feedback effects between different, possibly non-adjacent edges. This generalizes the setting that is common in the literature, where the only considered interactions take place at the boundary, i. e., in the nodes of the network. We discuss well-posedness of the associated initial value problem as well as contractivity and positivity properties of its solutions. Finally, we discuss qualitative properties that can be formulated in terms of invariance of linear subspaces of the state space, i. e., of symmetries of the associated physical system. Applications to a neurobiological model as well as to a system of linear Schroedinger equations on a quantum graph are discussed.Comment: 25 pages. Corrected typos and minor change

    Quantum ergodicity for graphs related to interval maps

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    We prove quantum ergodicity for a family of graphs that are obtained from ergodic one-dimensional maps of an interval using a procedure introduced by Pakonski et al (J. Phys. A, v. 34, 9303-9317 (2001)). As observables we take the L^2 functions on the interval. The proof is based on the periodic orbit expansion of a majorant of the quantum variance. Specifically, given a one-dimensional, Lebesgue-measure-preserving map of an interval, we consider an increasingly refined sequence of partitions of the interval. To this sequence we associate a sequence of graphs, whose directed edges correspond to elements of the partitions and on which the classical dynamics approximates the Perron-Frobenius operator corresponding to the map. We show that, except possibly for subsequences of density 0, the eigenstates of the quantum graphs equidistribute in the limit of large graphs. For a smaller class of observables we also show that the Egorov property, a correspondence between classical and quantum evolution in the semiclassical limit, holds for the quantum graphs in question.Comment: 20 pages, 1 figur

    Identification of glycosaminoglycan binding regions in the Plasmodium falciparum encoded placental sequestration ligand, VAR2CSA

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    <p>Abstract</p> <p>Background</p> <p>Pregnancy malaria is caused by <it>Plasmodium falciparum</it>-infected erythrocytes binding the placental receptor chondroitin sulfate A (CSA). This results in accumulation of parasites in the placenta with severe clinical consequences for the mother and her unborn child. Women become resistant to placental malaria as antibodies are acquired which specifically target the surface of infected erythrocytes binding in the placenta. VAR2CSA is most likely the parasite-encoded protein which mediates binding to the placental receptor CSA. Several domains have been shown to bind CSA <it>in vitro</it>; and it is apparent that a VAR2CSA-based vaccine cannot accommodate all the CSA binding domains and serovariants. It is thus of high priority to define minimal ligand binding regions throughout the VAR2CSA molecule.</p> <p>Methods</p> <p>To define minimal CSA-binding regions/peptides of VAR2CSA, a phage display library based on the entire <it>var2csa </it>coding region was constructed. This library was screened on immobilized CSA and cells expressing CSA resulting in a limited number of CSA-binding phages. Antibodies against these peptides were affinity purified and tested for reactivity against CSA-binding infected erythrocytes.</p> <p>Results</p> <p>The most frequently identified phages expressed peptides residing in the parts of VAR2CSA previously defined as CSA binding. In addition, most of the binding regions mapped to surface-exposed parts of VAR2CSA. The binding of a DBL2X peptide to CSA was confirmed with a synthetic peptide. Antibodies against a CSA-binding DBL2X peptide reacted with the surface of infected erythrocytes indicating that this epitope is accessible for antibodies on native VAR2CSA on infected erythrocytes.</p> <p>Conclusion</p> <p>Short continuous regions of VAR2CSA with affinity for multiple types of CSA were defined. A number of these regions localize to CSA-binding domains and to surface-exposed regions within these domains and a synthetic peptide corresponding to a peptide sequence in DBL2 was shown to bind to CSA and not to CSC. It is likely that some of these epitopes are involved in native parasite CSA adhesion. However, antibodies directed against single epitopes did not inhibit parasite adhesion. This study supports phage display as a technique to identify CSA-binding regions of large proteins such as VAR2CSA.</p
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