'Trapped rainbow' storage of light in metamaterials

Light usually propagates inside transparent materials in well known ways. However, recent research has examined the possibility of modifying the way the light travels by taking a normal transparent dielectric and inserting tiny metallic inclusions of various shapes and arrangements. As light passes through these structures, oscillating electric currents are set up that generate electromagnetic field moments; these can lead to dramatic effects on the light propagation, such as negative refraction. Possible applications include lenses that break traditional diffraction limits and 'invisibility cloaks' (refs 5, 6). Significantly less research has focused on the potential of such structures for slowing, trapping and releasing light signals. Here we demonstrate theoretically that an axially varying heterostructure with a metamaterial core of negative refractive index can be used to efficiently and coherently bring light to a complete standstill. In contrast to previous approaches for decelerating and storing light, the present scheme simultaneously allows for high in-coupling efficiencies and broadband, room-temperature operation. Surprisingly, our analysis reveals a critical point at which the effective thickness of the waveguide is reduced to zero, preventing the light wave from propagating further. At this point, the light ray is permanently trapped, its trajectory forming a double light-cone that we call an 'optical clepsydra'. Each frequency component of the wave packet is stopped at a different guide thickness, leading to the spatial separation of its spectrum and the formation of a 'trapped rainbow'. Our results bridge the gap between two important contemporary realms of science-metamaterials and slow light. Combined investigations may lead to applications in optical data processing and storage or the realization of quantum optical memories.     

Caveolin-1 interacts with the chaperone complex TCP-1 and modulates its protein folding activity

We report that caveolin-1, one of the major structural protein of caveolae, interacts with TCP-1, a hetero-oligomeric chaperone complex present in all eukaryotic cells that contributes mainly to the folding of actin and tubulin. The caveolin-TCP-1 interaction entails the first 32 amino acids of the N-terminal segment of caveolin. Our data show that caveolin-1 expression is needed for the induction of TCP-1 actin folding function in response to insulin stimulation. Caveolin-1 phosphorylation at tyrosine residue 14 induces the dissociation of caveolin-1 from TCP-1 and activates actin folding. We show that the mechanism by which caveolin-1 modulates TCP-1 activity is indirect and involves the cytoskeleton linker filamin. Filamin is known to bind caveolin-1 and to function as a negative regulator of insulin-mediated signaling. Our data support the notion that the caveolin-filamin interaction contributes to restore insulin-mediated phosphorylation of caveolin, thus allowing the release of active TCP-1. Received 17 November 2005; received after revision 1 December 2005; accepted 17 February 2006     

MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity

Following homozygosity mapping in a single kindred, we identified nonsense and missense mutations in MYO5B, encoding type Vb myosin motor protein, in individuals with microvillus inclusion disease (MVID). MVID is characterized by lack of microvilli on the surface of enterocytes and occurrence of intracellular vacuolar structures containing microvilli. In addition, mislocalization of transferrin receptor in MVID enterocytes suggests that MYO5B deficiency causes defective trafficking of apical and basolateral proteins in MVID.     

Ultrastructure of Eocene fossil plants

Petrified leaf and pericarpic tissues from the Eocene Deccan Intertrappean beds of India were studied using light and transmission electron microscopy. Degradated cytoplasm with organellelike bodies are present in cells of the leaf tissues. TEM of these cells revealed wall structure and cytoplasmic residues. Microfibril distribution of pericarpic cells resembles fiber cells in extant angiosperms.     

Mast cells in the skin of normal,hairless and athymic mice

Summary The skin of congenitally athymicnu/nu mice is rich in mast cells which stain metachromatically, contain histamine and 5-hydroxytryptamine, and participate in the PCA reaction. Mast cells of athymic mice have thus the attributes of normal mast cells.This work was supported by grants from the Swiss National Science Foundation (No. 3.516.71 and 3.234.74) and the Fritz Hoffmann-La-Roche-Stiftung.The skilful technical assistance of MissR. Keist is gratefully acknowledged.     

Changes in cellular noradrenaline fluorescence in the denervated rat superior cerical ganglion

Summary The microfluorimetrical investigation showed that in the principal perikarya of the rat superior cervical ganglion, after inhibition of noradrenaline-synthesis and unilateral preganglionic axotomy, the fluorescence of newly synthesized noradrenaline was most intense at the periphery of the perikarya of the intact side.The authors are deeply indebted to Mr H. Petermann, and to Mr B. Rombach, Ciba-Geigy Ltd. for their mathematical support.     

Direct measurement of proton transfer rates to a group controlling the dihydropyridine-sensitive Ca2+ channel

Protons participate in most biologically important reactions, as substrates, products, cofactors and modulators, and proton transport is an essential step in energy transduction. The dynamics of protonation reactions have been studied extensively in solution and in model systems involving lipid-water interfaces, but have never been resolved at the timescale of the elementary molecular event. Here we show that, under appropriate conditions, binding and unbinding reactions of single protons and deuterium ions to a single site on the L-type calcium channel can be resolved and the protonation and deprotonation rates quantified. The protonation rate constant considerably exceeds previous estimates obtained in simpler systems. The functional consequences of channel protonation is a threefold reduction of the channel conductance, independent of the applied voltage. The data are consistent with the presence of a single protonatable group with pK in the physiological pH range, close to the external mouth of the channel. The two conductance levels of the open channel might be explained by greatly differing local potentials associated with the protonated and deprotonated state of the group.     

A tissue-selective prostaglandin E2 analog with potent antifertility effects.

N-methanesulfonyl 16-phenoxy-omega-tetranor PGE2 is a prostaglandin analog which is markedly more tissue selective than PGE2. This compound is 10-30 times more potent than PGE2 in animal models which are considered relevant to antifertility effects in humans. In pharmacological tests which are believed to be predictive for side effects in humans, the compound has potency either equal to or less than that of PGE2.     

Die Abhängigkeit der Ca++-Aufnahme isolierter Mitochondrien des Herzmuskels von der Na+-und K+-Konzentration als mögliche Ursache der inotropen Digitaliswirkung

Summary In isolated mitochondria of heart muscle from rabbits and oxen there is, under suitable conditions, an accumulation of Ca⁺⁺, which is significantly enhanced by elevating the K⁺/Na⁺ quotient of the incubation medium. K-strophanthine (10^–5–10^–7) does not influence the accumulation of Ca⁺⁺ by the mitochondria of heart muscle. Therefore the intracellular increase in exchangeable Ca⁺⁺ observed after digitalis-glycosides could be explained by a decrease of the intracellular K⁺/Na⁺ quotient, which is caused by inhibition of the membrane ATPase and diminishes the capacity for Ca⁺⁺ accumulation in mitochondria.