Limitations in quantitation of the biomarker CCL18 in Gaucher disease blood samples by surface-enhanced laser desorption/ionization time-of-flight mass spectrometry

SELDI-TOF MS assisted the discovery of the chemokine CCL18/PARC as plasma biomarker for pathological storage cells in Gaucher disease patients. Prognostic elevation of CCL18 in blood of Gaucher patients has been confirmed by ELISA. Given its low molecular mass, positive charge, and relatively high abundance, CCL18 seems a particular attractive protein for SELDI-TOF based quantitation. Therefore, we determined CCL18 levels in plasma using SELDI-TOF MS and ELISA, in parallel. CCL18 levels in some blood samples were significantly underestimated when determined by SELDI-TOF MS. Spiking of recombinant CCL18 indicated that its detection by SELDI-TOF MS is strongly determined by the nature of the sample, even markedly varying between samples obtained from one donor at different time points. Independent of the total CCL18 concentration in blood only 1-10% of the chemokine bound to the ProteinChip Array. Even when comparable amounts of CCL18 from distinct samples were bound to the ProteinChip Array, diverse peak intensities could be observed. Thus, limited binding capacity and sample-dependent suppression of CCL18 ionization contribute significantly to the final peak intensity. In conclusion, SELDI-TOF MS offers no reliable procedure to quantitatively monitor CCL18 levels in blood and thus cannot be applied in evaluation of disease status of Gaucher patients.     

High throughput therapeutic drug monitoring of clozapine and metabolites in serum by on-line coupling of solid phase extraction with liquid chromatography-mass spectrometry

The characteristics of automated on-line solid phase extraction with liquid chromatography-mass spectrometry (SPE-LC-MS) are very amenable for flexibility and throughput in therapeutic drug monitoring (TDM). We demonstrate this concept of automated, on-line SPE-LC-MS for the analysis of clozapine and metabolites (desmethylclozapine and clozapine-N-oxide) in serum. Method development, optimisation and validation are described and a comparison with previously published methods for the determination of clozapine and metabolites in serum and plasma is made. Optimisation of chromatographic and SPE conditions for increased throughput resulted in SPE-LC-MS cycle times of only about 2.2 min, demonstrating the great potential of automated on-line SPE-LC-MS for TDM. The new method is shown to be clearly favourable, in particular in terms of ease of sample handling, throughput and detection limits. Recovery is essentially quantitative. Detection limits are at about 0.15-0.3 ng ml(-1), depending on the ionisation source used. Calibration follows a quadratic model for clozapine and its N-oxide and a linear model for the desmethyl metabolite (all cases: R > 0.99). Accuracy, evaluated at three concentration levels spanning the whole therapeutic range, shows that bias is less than 10%. Precision (intra - and inter assay) ranges from about 5% R.S.D. at the high end of the therapeutic range (700-1,000 ng ml(-1)) to about 20% R.S.D. (OECD defined limit) at the lower limit of quantitation ( approximately 50 ng ml(-1)). The lower limit of quantitation is well below the low end of the therapeutic range at 350 ng ml(-1).     

Improving Perovskite Solar Cells: Insights From a Validated Device Model

To improve the efficiency of existing perovskite solar cells (PSCs), a detailed understanding of the underlying device physics during their operation is essential. Here, a device model has been developed and validated that describes the operation of PSCs and quantitatively explains the role of contacts, the electron and hole transport layers, charge generation, drift and diffusion of charge carriers and recombination. The simulation to the experimental data of vacuum‐deposited CH₃NH₃PbI₃ solar cells over multiple thicknesses has been fit and the device behavior under different operating conditions has been studied to delineate the influence of the external bias, charge‐carrier mobilities, energetic barriers for charge injection/extraction and, different recombination channels on the solar cell performance. By doing so, a unique set of material parameters and physical processes that describe these solar cells is identified. Trap‐assisted recombination at material interfaces is the dominant recombination channel limiting device performance and passivation of traps increases the power conversion efficiency (PCE) of these devices by 40%. Finally, guidelines to increase their performance have been issued and it is shown that a PCE beyond 25% is within reach.     

Influence of streamflow on spawning‐related movements of golden perch Macquaria ambigua in south‐eastern Australia

In this study, linkages were examined between movement and spawning behaviour for golden perch Macquaria ambigua in a lowland river by integrating acoustic telemetry and egg and larval drift sampling over 4 years. Movement was strongly seasonal, being most prevalent during the spawning season (spring to early summer), and occurred primarily downstream into the lower river reaches during elevated flows. A very strong association was found between the occurrence of spawning and long‐distance M. ambigua movement. The results also revealed that targeted environmental water allocation can promote movement and spawning of this species. By integrating multiple analytical approaches and focusing on key life‐history events, this study provides an improved picture of the life history and flow requirements of M. ambigua. The findings can help guide the development of effective environmental flow recommendations.     

Population dynamics of calanoid copepods and the implications of their predation by clupeid fish in the Central Baltic Sea

Population dynamics of major Baltic calanoid copepod speciesin the Gotland Basin during the last two decades were characterizedby a decline of Pseudocalanus elongatus associated with decliningsalinities, and an increase of Temora longicornis and Acartiaspp. potentially due to warmer conditions. Additionally thisstudy investigated the effect of predation by the major planktivorousfish species herring (Clupea harengus) and sprat (Sprattus sprattus)for the period 1977–1996 in the Gotland Basin (CentralBaltic Sea). Examination of consumption by these fish speciesin relation to copepod production estimates showed a switchby herring from consuming mainly CV/VI of P. elongatus and T.longicornis, to preying on CII of the latter copepod. This switchwas potentially due to increased competition with the drasticallyincreased sprat stock since the late 1980s. Further, an increasedpredation pressure by sprat on CV/CVI of both copepod speciesin spring resulted in higher copepod mortality rates. In consequence,based on these results we suggest that the increase in the spratstock since the late 1980s contributed to a decline of P. elongatus,and additionally prevented an even more pronounced temperature-drivenincrease in the T. longicornis stock, as was observed for Acartiaspp., which was not significantly consumed.     

Water crystallization within rat precision-cut liver slices in relation to their viability

This study examined whether tissue vitrification, promoted by partitioning within the tissue, could be the mechanism explaining the high viability of rat liver slices, rapidly frozen after preincubation with 18% Me2SO or VS4 (a 7.5 M mixture of Me2SO, 1,2-propanediol, and formamide with weight ratio 21.5:15:2.4). To achieve this, we first determined the extent to which crystallization or vitrification occurred in cryoprotectant solutions (Me2SO and VS4) and within liver slices impregnated with these solutions. Second, we determined how these events were related to survival of slices after thawing. Water crystallization was evaluated by differential scanning calorimetry and viability was determined by histomorphological examination of the slices after culturing at 37 degrees C for 4 h. VS4-preincubated liver slices indeed behaved differently from bulk VS4 solution, because, when vitrified, they had a lower tendency to devitrify. Vitrified VS4-preincubated slices that were warmed sufficiently rapid to prevent devitrification had a high viability. When VS4 was diluted (to 75%) or if warming was not fast enough to prevent ice formation, slices had a low viability. With 45% Me2SO, low viability of cryopreserved slices was caused by cryoprotectant toxicity. Surprisingly, liver slices preincubated with 18% Me2SO or 50% VS4 had a high viability despite the formation of ice within the slice. In conclusion, tissue vitrification provides a mechanism that explains the high viability of VS4-preincubated slices after ultrarapid freezing and thawing (>800 degrees C/min). Slices that are preincubated with moderately concentrated cryoprotectant solutions (18% Me2SO, 50% VS4) and cooled rapidly (100 degrees C/min) survive cryopreservation despite the formation of ice crystals within the slice.     

Toward tailored exosomes: the exosomal tetraspanin web contributes to target cell selection

Exosomes are discussed as potent therapeutics due to efficient transfer of proteins, mRNA and miRNA in selective targets. However, therapeutic exosome application requires knowledge on target structures to avoid undue delivery. Previous work suggesting exosomal tetraspanin-integrin complexes to be involved in target cell binding, we aimed to control this hypothesis and to define target cell ligands. Exosomes are rich in tetraspanins that associate besides other molecules with integrins. Co-immunoprecipitation of exosome lysates from rat tumor lines that differ only with respect to Tspan8 and beta4 revealed promiscuity of tetraspanin-integrin associations, but also few preferential interactions like that of Tspan8 with alpha4 and beta4 integrin chains. These minor differences in exosomal tetraspanin-complexes strongly influence target cell selection in vitro and in vivo, efficient exosome-uptake being seen in hematopoietic cells and solid organs. Exosomes expressing the Tspan8-alpha4 complex are most readily taken up by endothelial and pancreas cells, CD54 serving as a major ligand. Selectivity of uptake was confirmed with exosomes from an alpha4 cDNA transfected Tspan8(+) lymph node stroma line. Distinct from exosomes from the parental line, the latter preferentially targeted endothelial cells and in vivo the pancreas. Importantly, pulldown experiments provided strong evidence that exosome-uptake occurs in internalization-prone membrane domains. This is the first report on the exosomal tetraspanin web contributing to target cell selection such that predictions can be made on potential targets, which will facilitate tailoring exosomes for drug delivery.     

Enhanced reactivation and mutagenesis after transfection of carcinogen-treated monkey kidney cells with UV-irradiated simian virus 40 (SV40) DNA

Monkey kidney cells, either untreated or pretreated with UV-light at 254 nm or mitomycin C, were transfected 24 hours later with the intact or UV-irradiated DNA from the thermosensitive tsB201 simian virus 40 mutant unable to grow at 41 degrees C. The survival of the viral progeny obtained from the UV-irradiated DNA is increased in pretreated cells compared to the survival of the viral progeny obtained in untreated cells. Irradiation of the viral DNA enhances the reversion frequency of the viral progeny towards a wild type phenotype able to grow at 41 degrees C. Pretreatment of the cells with UV or mitomycin C does not increase the reversion frequency.     

Eastern deciduous tree seedlings advance spring phenology in response to experimental warming,but not wetting,treatments

Changing global climate, particularly rising temperatures, has been linked through observations with advanced spring phenology in temperate regions. We experimentally tested if regional climate change predictions of increased temperature and precipitation alter the spring phenology of eastern US tree seedlings. This study reports the results of a 3-year-field experiment designed to study the responses of eastern deciduous tree species planted in a post-harvest environment to a 2 °C increase in temperature and a 20 % increase in precipitation. Species were monitored for timing of germination and leaf out in four treatment combinations (ambient, warmed, irrigated, and warmed + irrigated) on 16 plots located in a recently harvested central Pennsylvania forest. The 2 °C warming advanced day of seed germination by an average of 2 weeks and seedling leaf out by 10 days among all species (both p < 0.001). However, increased precipitation did not result in a significant change in spring phenology. Species responded uniquely to treatments, with germination advancing in three of five species in response to warming and leaf out advancing in six of six species. Southern species projected to expand northward into the study region with rising temperatures did not show responses to warming treatments that would provide them an advantage over current resident species. Timing of germination and leaf out varied among years of the experiment, most likely driven by year-to-year variability in spring temperatures. The climate change experiment highlighted the potential of a moderate 2 °C temperature increase to advance spring phenology of deciduous tree seedlings by up to 2 weeks, with a lack of a phenological response to a 20 % increase in precipitation.