Mechanisms determining the salience of coloration in echoed sound: influence of interaural time and level differences

This study investigates whether the salience of the pitch associated with a single reflection of a broadband sound, such as noise, is determined by the monaural information mediated by the stimuli at the two ears, or by the relative locations of the primary sound and the reflection. Pitch strength was measured as a function of the reflection delay and the lateral displacement between the primary sound and the reflection. Thereby, lateral displacement was produced by means of interaural time differences (ITDs) in experiment 1 and interaural level differences (ILDs) in experiment 3. The results from both experiments are in accordance with the assumption that the strength of the pitch associated with a reflection is based on a central average of the internal representations of the stimuli at the two ears. This notion was corroborated by experiment 2, which showed that the results from experiment 1 could be mimicked by simply adding the stimuli from the two ears and presenting the merged stimulus identically to both ears.     

Differential analysis of phosphorylated proteins in resting and thrombin-stimulated human platelets

Blood platelets are important components of haemostasis. After their activation they cause healing of wounds by forming plugs and initiate repair processes. One important event in regulating this activation is the phosphorylation/dephosphorylation of multiple proteins on various tyrosine, serine and threonine residues. To understand the exact molecular mechanisms in platelet activation it is essential to identify proteins involved in the signalling pathways and to localise and characterise their phosphorylation sites. After treatment with ³²P and separation by 2D-PAGE using different pI ranges, phosphorylated platelet proteins were detected by autoradiography. Phosphotyrosine-containing proteins were assigned by immunoblotting with an anti-phosphotyrosine antibody. Another approach for the identification of phosphorylated proteins was immunoprecipitation of tyrosine-phosphorylated proteins using an anti-phosphotyrosine antibody. Protein spots/bands of interest were excised from the gel, digested with trypsin and analysed by MALDI-TOF-MS and nano-LC-ESI-MS/MS, respectively. Several phosphorylated proteins could be identified and the localisation of some in vivo phosphorylation sites was possible.Abbreviations DTT 1,4-dithiothreitol - HCCA -cyano-4-hydroxycinnamic acid - PMSF phenylmethylsulfonylfluoride - PSD post source decay - TFA trifluoroacetic acid - TOF time-of-flight     

Special Moufang sets, their root groups and their {micro}-maps

We prove Timmesfeld's conjecture that special abstract rankone groups are quasisimple. We give two characterizations ofthe root groups in special Moufang sets: a normal subgroup ofthe point stabilizer is a root group if it is either regular,or nilpotent and transitive. We prove that if a root group ofa special Moufang set contains an involution, then it is ofexponent 2. We also show that the root groups are abelian ifand only if the so-called µ-maps are involutions.     

Efficient high-power frequency doubling of distributed Bragg reflector tapered laser radiation in a periodically poled MgO-doped lithium niobate planar waveguide

We report on efficient single-pass, high-power second-harmonic generation in a periodically poled MgO-doped LiNbO3 planar waveguide using a distributed Bragg reflector tapered diode laser as a pump source. A coupling efficiency into the planar waveguide of 73% was realized, and 1.07 W of visible laser light at 532 nm was generated. Corresponding optical and electro-optical conversion efficiencies of 26% and 8.4%, respectively, were achieved. Good agreement between the experimental data and the theoretical predictions was observed.     

Synthesis of Chiral Cyclohexenones from α-Campholenic,Fencholenic, and β-Campholenic Derivatives

Summary. Optically active dimethylcyclohexenones, potential building blocks for enantioselective syntheses of various naturally active substances, were prepared. These compounds were obtained by oxidation with KMnO₄/Pb(OAc)₄ or ozonolysis of the corresponding cyclopentenic precursors, followed by aldol condensation. During the course of the preparation intermediate diols and chiral polyfunctional carbonyl derivatives were separated and identified analytically.     

Visualization of Protein‐Specific Glycosylation inside Living Cells

Protein glycosylation is a ubiquitous post‐translational modification that is involved in the regulation of many aspects of protein function. In order to uncover the biological roles of this modification, imaging the glycosylation state of specific proteins within living cells would be of fundamental importance. To date, however, this has not been achieved. Herein, we demonstrate protein‐specific detection of the glycosylation of the intracellular proteins OGT, Foxo1, p53, and Akt1 in living cells. Our generally applicable approach relies on Diels–Alder chemistry to fluorescently label intracellular carbohydrates through metabolic engineering. The target proteins are tagged with enhanced green fluorescent protein (EGFP). Förster resonance energy transfer (FRET) between the EGFP and the glycan‐anchored fluorophore is detected with high contrast even in presence of a large excess of acceptor fluorophores by fluorescence lifetime imaging microscopy (FLIM).