Studies on film potentiometric stripping analysis: effects of electrochemical parameters

Film potentiometric stripping analysis (PSA) is a novel method for concentrating the test ion directly on a glassy carbon electrode with subsequent stripping by a chemical oxidant, the redissolution step being followed by a chronopotentiometric sequence. The electrochemical parameters governing both preconcentration and redissolution steps are studied on a rotating disk electrode: experimental results are compared with the theoretical developments recently published. Except for the influence of rde rotation rates on each step and on analytical parameters, experiments and theory are in agreement. Discrepancies concerning the rotation rate effects are studied by potentiostatic coulometry and voltammetry measurements in regard to the preconcentration step: the rotation rate effects are based on the physical behaviour of the rde. Routine analysis is carried out using film PSA, Pb(II) as the test ion and Fe(III) as oxidizing agent, in perchlorate medium.     

德国迪林根ROGESA钢铁公司2号烧结机EFA(R)烟气处理系统及其运转情况

多年来,环境保护一直是烧结行业的一个重要课题.由于政府部门提出了更加严格的要求,烧结厂废气的进一步净化已经变得很有必要.一套新开发的、工业化的EFA(曳流吸收塔)烟气处理系统于2006年年中在ROGESA钢铁公司投入运行.本文就该系统的工艺流程、特点及运行情况作一介绍.     

Crystal Structure of the Human Monoacylglycerol Lipase,a Key Actor in Endocannabinoid Signaling

2‐Arachidonoylglycerol plays a major role in endocannabinoid signaling, and is tightly regulated by the monoacylglycerol lipase (MAGL). Here we report the crystal structure of human MAGL. The protein crystallizes as a dimer, and despite structural homologies to haloperoxidases and esterases, it distinguishes itself by a wide and hydrophobic access to the catalytic site. An apolar helix covering the active site also gives structural insight into the amphitropic character of MAGL, and likely explains how MAGL interacts with membranes to recruit its substrate. Docking of 2‐arachidonoylglycerol highlights a hydrophobic and a hydrophilic cavity that accommodate the lipid into the catalytic site. Moreover, we identified Cys201 as the crucial residue in MAGL inhibition by N‐arachidonylmaleimide, a sulfhydryl‐reactive compound. Beside the advance in the knowledge of endocannabinoids degradation routes, the structure of MAGL paves the way for future medicinal chemistry works aimed at the design of new drugs exploiting 2‐arachidonoylglycerol transmission.     

X-Ray Micro-Calorimeter Based on Si Thermistors for X-Ray Astronomy: Design and First Measurements

X-ray Astronomy provides a unique window on a wide variety of astrophysical phenomena. The currently operating X-ray space observatories perform X-ray spectral imaging with the use of CCDs. When available, cryogenic X-ray microcalorimeter arrays will far outperform CCDs in terms of spectral resolution, energy bandwidth and count rate. Experience has been gained with Infra-Red bolometer arrays at CEA-LETI (Grenoble) in collaboration with the CEA-SAp (Saclay); taking advantage of this background, we are now developing an X-ray spectro-imaging camera for the next generation space astronomy missions, using silicon technology (implanted and high temperature diffused thermistors). Each pixel of this array detector is made of a tantalum absorber bound, by indium bump hybridization, to a silicon thermistor. The absorber array is bound to the thermistor array in a single automatic step. The thermo-mechanical link, provided by hybridization, is being improved in terms of thermal capacitance. Finally, our main effort is in developing arrays of silicon thermistors with negligible excess 1/f noise. The thermistor has been simulated with the 2D simulator ATHENA (SILVACO International). We studied the effects of the implants and their thermal treatment on both vertical and lateral dopant distributions at the edges of the thermistor. Prototypes have been created following the procedure optimized by the ATHENA simulation. We present the status of the development and results of measurements performed on these four main building blocks required to create a detector array up to 32×32 pixels in size.      

Screening of Yeast Display Libraries of Enzymatically Treated Peptides to Discover Macrocyclic Peptide Ligands

We present the construction and screening of yeast display libraries of post-translationally modified peptides wherein site-selective enzymatic treatment of linear peptides is achieved using bacterial transglutaminase. To this end, we developed two alternative routes, namely (i) yeast display of linear peptides followed by treatment with recombinant transglutaminase in solution; or (ii) intracellular co-expression of linear peptides and transglutaminase to achieve peptide modification in the endoplasmic reticulum prior to yeast surface display. The efficiency of peptide modification was evaluated via orthogonal detection of epitope tags integrated in the yeast-displayed peptides by flow cytometry, and via comparative cleavage of putative cyclic vs. linear peptides by tobacco etch virus (TEV) protease. Subsequently, yeast display libraries of transglutaminase-treated peptides were screened to isolate binders to the N-terminal region of the Yes-Associated Protein (YAP) and its WW domains using magnetic selection and fluorescence activated cell sorting (FACS). The identified peptide cyclo[E-LYLAYPAH-K] featured a K_D of 1.75 μM for YAP and 0.68 μM for the WW domains of YAP as well as high binding selectivity against albumin and lysozyme. These results demonstrate the usefulness of enzyme-mediated cyclization in screening combinatorial libraries to identify cyclic peptide binders.     

Thiorphan stimulates clonal growth of GM-CFU in short-term cultures of bone marrow from a healthy donor and from patients with non-Hodgkin lymphoma

Thiorphan, a specific inhibitor of membrane neutral endopeptidase (NEP, EC 3.4.24.11) also known as the common acute lymphoblastic leukemia antigen (CALLA, CD10) was added into short-term clonal cultures of the buffy coat concentrates of human bone marrow obtained from a healthy donor (six experiments) and from ten patients with non-Hodgkin lymphoma (NHL) (eight in complete remission, one in partial remission and one in relapse). Thiorphan concentrations ranged from 10(-5) to 10(-13) M. Nanomolar and higher concentrations of the drug mildly stimulated the granulocyte-macrophage colony-forming unit (GM-CFU) counts in the cultures of normal bone marrow, reaching the significance at 10(-7) M. Meaningful alterations of the GM-CFU counts were noted in 31 of 79 thiorphan-treated cultures of NHL bone marrow (39%). In those cultures the stimulatory effects (33%) outnumbered the inhibitory ones (6%). The stimulatory effects occurred mainly in the bone marrow samples of the patients with highly malignant NHL. The observations are compatible with the idea that the membrane endopeptidase (CALLA, CD10) participates in processes controlling the proliferation and differentiation of hematopoetic cells by cleaving the neuropeptides and related hemoregulatory peptides.     

Production of a high purity F radioactive beam

An efficient method for the production and post-acceleration of a pure ¹⁸F(T_1/2=109.8 min) radioactive beam has been developed. Large amounts of ¹⁸F are produced via the ¹⁸O(p,n)¹⁸F reaction using a 15.5 MeV proton beam on an ¹⁸O-enriched water target. After the chemical purification of the target content, the ¹⁸F activity is transferred into [¹⁸F]-fluoromethane. It is then transported to an ECR ion source, where after dissociation of the molecules, the fluorine atoms are ionized. Finally, the ¹⁸F²⁺ ions are accelerated to 14 MeV in a second cyclotron. The different steps in the production cycle and the characteristics of the final ¹⁸F beam are discussed.