A novel method to identify and characterise peptide mimotopes of heat shock protein 70-associated antigens

The heat shock protein, Hsp70, has been shown to play an important role in tumour immunity. Vaccination with Hsp70-peptide complexes (Hsp70-PCs), isolated from autologous tumour cells, can induce protective immune responses. We have developed a novel method to identify synthetic mimic peptides of Hsp70-PCs and to test their ability to activate T-cells. Peptides (referred to as "recognisers") that bind to Hsp70-PCs from the human breast carcinoma cell line, MDA-MB-231, were identified by bio-panning a random peptide M13 phage display library. Synthetic recogniser peptides were subsequently used as bait in a reverse bio-panning experiment to identify potential Hsp70-PC mimic peptides. The ability of the recogniser and mimic peptides to prime human lymphocyte responses against tumour cell antigens was tested by stimulating lymphocytes with autologous peptide-loaded monocyte-derived dendritic cells (DCs). Priming and subsequent stimulation with either the recogniser or mimic peptide resulted in interferon-γ (IFN-γ) secretion by the lymphocytes. Furthermore, DCs loaded with Hsp70, Hsp70-PC or the recogniser or the mimic peptide primed the lymphocytes to respond to soluble extracts from breast cells. These results highlight the potential application of synthetic peptide-mimics of Hsp70-PCs, as modulators of the immune response against tumours.     

Comment on "microstructured polymer fiber laser"

We comment on the recent Letter by Argyros et al. [Opt. Lett. 29, 1882 (2004)] in which a microstructured polymer fiber doped with the dye Rhodamine 6G was discussed as a possible fiber laser source. We suggest that the lasing action at 632 nm was due to stimulated Raman scattering in the poly(methyl methacrylate) host material.     

Powerful red-green-blue laser source pumped with a mode-locked thin disk laser

We present a red-green-blue laser source with average powers of 8 W in the red, 23 W in the green, and 10.1 W in the blue. The entire pump power for the nonlinear conversion stages is provided by a single laser oscillator without any amplifier stages. Our system does not require any synchronized cavities, and all nonlinear crystals except one are critically phase matched at room temperature.     

Mechanism of bleomycin suicide: a Car-Parrinello molecular dynamics investigation

Using first-principles molecular dynamics simulations (Car-Parrinello method) we investigated the possible reaction pathways for decay of the active bleomycin-Fe(III)-OOH complex, so-called bleomycin suicide. The theoretical model of activated bleomycin contains the whole metal bonding domain of the bleomycin ligand. Simulations performed both in a vacuum and in water show that a facile decaying process involves a homolytic O-O bond cleavage with an almost simultaneous hydrogen atom abstraction. The formation of an intra- or intermolecular hydrogen bond appears to be crucial for the decay of the activated bleomycin. We did not observe any evidence of heterolytic cleavage of the O-O bond of the Fe(III)-OOH species.     

Accelerating rare reactive events by means of a finite electronic temperature

The range of chemical problems that are directly accessible to first-principles molecular dynamics simulations based on density functional theory is extended with a novel method apt to accelerate rare reactive events. The introduction of a finite electronic temperature within the Mermin formalism leads to a lowering of chemical activation barriers and thus to an exponential enhancement of the rate at which these reactions are observed during a first-principles molecular dynamics simulation. The method presented here makes direct use of the intrinsic chemical information encoded in the electronic structure, and is therefore able to lower selectively chemically relevant activation energies even in systems where many competing low-energy pathways for conformational transitions or diffusive motions are present. The performance of this new approach is demonstrated for a series of prototypical chemical reactions in gas and in condensed phase. A typical acceleration that can be achieved is, for example, a factor of 10(5) for the cis-trans isomerization of peroxynitrous acid in aqueous solution at room temperature.     

A multimethod for the determination of 150 pesticide metabolites in surface water and groundwater using direct injection liquid chromatography–mass spectrometry

Based on the information available on 293 pesticides (herbicides, insecticides, fungicides, biocides, growth regulators) 210 pesticide metabolites were selected for inclusion into a multimethod for the analysis of ground and surface water. With the final method 150 pesticide metabolites can be analysed from groundwater and surface water by direct injection-liquid chromatography–electrospray ionization-tandem mass spectrometry with multiple-reaction monitoring. For most of these metabolites this is the first method published. For all metabolites linear calibration in drinking water was possible, with a lower limit of calibration of 0.1 μg/L achieved for 142 analytes and of 0.01 μg/L for 113 of the analytes. Matrix effects in ground and surface water compared to those in the drinking water were moderate (±20%) for 87% of the analytes. For critical sample/analyte combinations standard addition has to be used for correct quantification. This method allows for an extensive study of the occurrence of previously unknown or undetectable pesticide metabolites in groundwaters and surface waters.     

1,6-Anhydrofuranosen,XVIII. Wahlweise Cyclisieruhg Eines D-Allose-Deriyates Zur 1,6-Anhydrofuranose Oder Zum Furanoiden 1,6′:1,6-Dianhydrid

Abstract

Depending on reaction conditions 1,2-Di-O-acetyl-3,5,6-tri-O-benzyl-D-allofuranose (2b) can be cyclized with SnCl₄ either giving the monomeric 1,6-anhydrohexofuranose derivative 3a, as was already reported in a patent procedure, or by changing the solvent from methylene chloride to toluene giving the 1,6′:1′,6-dianhydride 4a mainly. The dimeric structure of compounds 4 was proved by CI-mass spectrometry. The ¹H-n.m.r. spectrum of the acetate 4d allowed us to deduce the conformation preferentially adopted by these dianhydrides.     

Die Anwendung von Formaldehyd zur Vermeidung von Artefacten bei der chromatographischen Bestimmung von Ketos?uren

Ohne Zusammenfassung     

Safety assessment of nanomaterials using an advanced decision-making framework,the DF4nanoGrouping

As presented at the 2016 TechConnect World Innovation Conference on 22–25 May 2016 in Washington DC, USA, the European Centre for Ecotoxicology and Toxicology of Chemicals (ECETOC) ‘Nano Task Force’ proposes a Decision-making framework for the grouping and testing of nanomaterials (DF4nanoGrouping) consisting of three tiers to assign nanomaterials to four main groups with possible further subgrouping to refine specific information needs. The DF4nanoGrouping covers all relevant aspects of a nanomaterial’s life cycle and biological pathways: intrinsic material properties and system-dependent properties (that depend upon the nanomaterial’s respective surroundings), biopersistence, uptake and biodistribution, and cellular and apical toxic effects. Use, release, and exposure route may be applied as ‘qualifiers’ to determine if, e.g., nanomaterials cannot be released from products, which may justify waiving of testing. The four main groups encompass (1) soluble, (2) biopersistent high aspect ratio, (3) passive, and (4) active nanomaterials. The DF4nanoGrouping foresees a stepwise evaluation of nanomaterial properties and effects with increasing biological complexity. In case studies covering carbonaceous nanomaterials, metal oxide, and metal sulfate nanomaterials, amorphous silica and organic pigments (all nanomaterials having primary particle sizes below 100 nm), the usefulness of the DF4nanoGrouping for nanomaterial hazard assessment was confirmed. The DF4nanoGrouping facilitates grouping and targeted testing of nanomaterials. It ensures that sufficient data for the risk assessment of a nanomaterial are available, and it fosters the use of non-animal methods. No studies are performed that do not provide crucial data. Thereby, the DF4nanoGrouping serves to save both animals and resources.