Political consequences of Germany's mixed-member system: Personalization at the grass-roots?

-- Dem deutschen Wahlsystem werden international einige Vorteile gegenüber anderen Wahlsystemen bescheinigt, die z.B. Neuseeland sogar zur Nachahmung angeregt haben. Als gemischtes Wahlsystem kombiniert es das Prinzip proportionaler Repräsentation mit einer Mehrheitskomponente. Wegen dieser Kombination wird ihm zum einen nachgesagt, Garant für ein stabiles Parteiensystem zu sein, und zum anderen, demokratietheoretisch proportionale Repräsentation und Mehrheitsentscheidung ideal zu kombinieren. Dieser Beitrag untersucht die Effekte des Wahlsystems auf die Größe des Parteiensystems und die Frage, inwieweit Wähler von den Möglichkeiten der beiden Komponenten des Wahlsystems, der Listen- und Direktwahl, also substantiell von der Partei- und Persönlichkeitswahl tatsächlich Gebrauch machen. Letzteres wird häufiger bestritten und behauptet, auch die Direktwahl der Abgeordneten im Wahlkreis folge lediglich parteienbezogenen Überlegungen. Die empirischen Ergebnisse zeigen anhand der Wahlrechtsänderungen in der Bundesrepublik, dass das Wahlsystem tatsächlich einen beträchtlichen Anteil an der Größe des Parteiensystems und damit der Stabilität des Parteiensystems hat. Sie zeigen zum anderen, dass die Möglichkeit der Listen- und Personenwahl zum einen mittels Stimensplitting strategisch zum Koalitionswählen genutzt wird, zum anderen der Wahlerfolg der Kandidaten im Wahlkreis aber durchaus davon anhängt, wie stark sie sich in der Sicht der Bürger für den Wahlkreis einsetzen und wie gut ihre politische Arbeit beurteilt wird. Es existiert also die Persönlichkeitswahl at the Grass-Roots.

Association of ABCB1, 5-HT3B receptor and CYP2D6 genetic polymorphisms with ondansetron and metoclopramide antiemetic response in Indonesian cancer patients treated with highly emetogenic chemotherapy.

Our study shows that in Indonesian cancer patients treated with highly cytostatic emetogenic, carriership of the CTG haplotype of the ABCB1 gene is related to an increased risk of delayed chemotherapy-induced nausea and vomiting

A large Eomys antiquus (Aymard, 1853) (Mammalia, Rodentia) from the early Oligocene sedimentary deposits at Bouldnor Cliff (Isle of Wight, England, UK)

A collection of approx. 150 isolated cheek teeth of the eomyid rodent Eomys antiquus which was obtained from a very thin layer in the HamsteadMember of the Bouldnor Formation at Bouldnor Cliff (Isle ofWight, England, UK) is described. The material is post-Grande Coupure, and earliest Oligocene in age. Comparison is made with and new data are given on teeth of Eomys from localities of a similar age situated elsewhere in Europe: Eomys antiquus from Hoogbutsel (Belgium), andMöhren 13, 19, and 20 (Germany), and Eomys aff. antiquus from Montalbán 1D (Spain), and Kocayarma (Turkish Thrace, Turkey). Teeth from Bouldnor Cliff and Hoogbutsel (Mammal Paleogene zone 21) are morphologically close to those from Möhren 13 (Mammal Paleogene zone 22), but tend to be larger. Size decrease in the course of time is also suggested by the smaller size of the teeth from Montalbán 1D (Mammal Paleogene zone 23). The morphological differences observed between the English, Belgian, and German material at the one side, and the Spanish and Turkish material at the other, confirm that the species from Montalbán 1D and Kocayarma is a different, although closely related form. The taxonomic history of Eomys antiquus is reviewed. The species is the commoner of the two oldest European Eomyidae known. General knowledge on the ecology of the eomyids suggests that at the time of deposition of the Eomys-containing layer in the Hampshire Basin forest was close by

A predicted physicochemically distinct sub-proteome associated with the intracellular organelle of the anammox bacterium Kuenenia stuttgartiensis

Medema MH, Zhou M, van Hijum SAFT, et al. A predicted physicochemically distinct sub-proteome associated with the intracellular organelle of the anammox bacterium Kuenenia stuttgartiensis. BMC Genomics. 2010;11(1): 299.Background Anaerobic ammonium-oxidizing (anammox) bacteria perform a key step in global nitrogen cycling. These bacteria make use of an organelle to oxidize ammonia anaerobically to nitrogen (N2) and so contribute ~50% of the nitrogen in the atmosphere. It is currently unknown which proteins constitute the organellar proteome and how anammox bacteria are able to specifically target organellar and cell-envelope proteins to their correct final destinations. Experimental approaches are complicated by the absence of pure cultures and genetic accessibility. However, the genome of the anammox bacterium Candidatus "Kuenenia stuttgartiensis" has recently been sequenced. Here, we make use of these genome data to predict the organellar sub-proteome and address the molecular basis of protein sorting in anammox bacteria. Results Two training sets representing organellar (30 proteins) and cell envelope (59 proteins) proteins were constructed based on previous experimental evidence and comparative genomics. Random forest (RF) classifiers trained on these two sets could differentiate between organellar and cell envelope proteins with ~89% accuracy using 400 features consisting of frequencies of two adjacent amino acid combinations. A physicochemically distinct organellar sub-proteome containing 562 proteins was predicted with the best RF classifier. This set included almost all catabolic and respiratory factors encoded in the genome. Apparently, the cytoplasmic membrane performs no catabolic functions. We predict that the Tat-translocation system is located exclusively in the organellar membrane, whereas the Sec-translocation system is located on both the organellar and cytoplasmic membranes. Canonical signal peptides were predicted and validated experimentally, but a specific (N- or C-terminal) signal that could be used for protein targeting to the organelle remained elusive. Conclusions A physicochemically distinct organellar sub-proteome was predicted from the genome of the anammox bacterium K. stuttgartiensis. This result provides strong in silico support for the existing experimental evidence for the existence of an organelle in this bacterium, and is an important step forward in unravelling a geochemically relevant case of cytoplasmic differentiation in bacteria. The predicted dual location of the Sec-translocation system and the apparent absence of a specific N- or C-terminal signal in the organellar proteins suggests that additional chaperones may be necessary that act on an as-yet unknown property of the targeted proteins

A small assemblage of early Oligocene rodents and insectivores from the Sivas basin, Turkey

The assemblage of small mammals from a site near Yeniköy (Anatolia) is described. The assemblage was collected by screen-washing a sample from a locality in the Selimye Formation (Sivas basin). The site has a magneto-stratigraphic calibrated age of 29 Ma (younger part of the early Oligocene). The murids dominate in this relatively small collection with Eucricetodon and Pseudocricetodon. In addition, a dipodid, an unidentified erinaceide and the new baluchimyin hystricognath genus and species Zorania milosi nov. gen. et nov. sp. are present. The study of Eucricetodon, Pseudocricetodon and Zorania nov. sp. includes an analysis of incisor enamel microstructure. The incisor microstructure of Eucricetodon shows that there are several parallel long-living lineages within the genus. The Anatolia-Balkans biogeography of the late Eocene-Oligocene is reviewed. Its rodent assemblages are characterised by dominance of murids and presence of taxa that are known from low-latitude Asia. The Paleogene Anatolia-Balkans biogeographic province, is therefore rather different from those of western European and the Indian subcontinent

On the antiquity and status of the Spalacidae, new data from the late Eocene of south-East Serbia

A new blind mole-rat species Debruijnia tintinnabulus nov. sp. is described from the late Eocene of south east Serbia. This find is approximately 10 Ma older than the hitherto oldest records of Spalacidae Vetusspalax and Pannoniamys, both from the late Oligocene of Bosnia and Herzegovina and Serbia. The antiquity of the new species (~34 Ma) is in accordance with recent genetically based age estimates of Spalacidae as an early branch of the Supramyomorpha. A review of the fossil record shows that the Spalacidae are probably not closely related to the Rhizomyinae and Myospalacinae. The spalacid finds from the Paleogene of the Balkans and the Neogene of Anatolia suggests that the family underwent a radiation during the Oligocene involving Debruijnia, Vetusspalax, Pannoniamys and Heramys. During the middle and late Miocene Heramys evolved into a large number of species, here all tentatively allocated to Pliospalax

Survey of T-2 and HT-2 toxins by LC–MS/MS in oats and oat products from European oat mills in 2005–2009

T-2 and HT-2 toxins were analysed in oats (n = 243), oat flakes (n = 529), oat meal (n = 105) and oat by-products (n = 209) from 11 European mills during 2005–2009 by high-performance liquid chromatography with a triple quadrupole mass spectrometer. Limits of quantification were 5 μg kg−1 for both T-2 and HT-2 toxins in oats. The incidence of T-2 + HT-2 (> 5 μg kg−1) in oats, oat flakes, oat meal and oat by-products was 93, 77, 34 and 99%, respectively. The mean values of T-2 + HT-2 were 94, 17, 11 and 293 μg kg−1 for oats, oat flakes, oat meal and oat by-products, respectively. T-2 and HT-2 occurred together and the T-2 level was 52% of HT-2 in oats. Maximal T-2 and HT-2 concentration in oat flakes and oat meal were 197 and 118 μg kg−1. The toxins were reduced by 82–88% during processing, but increased 3.1 times in oat by-products

The vaccine potential of Bordetella pertussis biofilm-derived membrane proteins

Pertussis is an infectious respiratory disease of humans caused by the gram-negative pathogen Bordetella pertussis. The use of acellular pertussis vaccines (aPs) which induce immunity of relative short duration and the emergence of vaccine-adapted strains are thought to have contributed to the recent resurgence of pertussis in industrialized countries despite high vaccination coverage. Current pertussis vaccines consist of antigens derived from planktonic bacterial cultures. However, recent studies have shown that biofilm formation represents an important aspect of B. pertussis infection, and antigens expressed during this stage may therefore be potential targets for vaccination. Here we provide evidence that vaccination of mice with B. pertussis biofilm-derived membrane proteins protects against infection. Subsequent proteomic analysis of the protein content of biofilm and planktonic cultures yielded 11 proteins which were ≥ three-fold more abundant in biofilms, of which Bordetella intermediate protein A (BipA) was the most abundant, surface-exposed protein. As proof of concept, mice were vaccinated with recombinantly produced BipA. Immunization significantly reduced colonization of the lungs and antibodies to BipA were found to efficiently opsonize bacteria. Finally, we confirmed that bipA is expressed during respiratory tract infection of mice, and that anti-BipA antibodies are present in the serum of convalescent whooping cough patients. Together, these data suggest that biofilm proteins and in particular BipA may be of interest for inclusion into future pertussis vaccines.Facultad de Ciencias ExactasCentro de Investigación y Desarrollo en Fermentaciones Industriale

The vaccine potential of Bordetella pertussis biofilm-derived membrane proteins

Pertussis is an infectious respiratory disease of humans caused by the gram-negative pathogen Bordetella pertussis. The use of acellular pertussis vaccines (aPs) which induce immunity of relative short duration and the emergence of vaccine-adapted strains are thought to have contributed to the recent resurgence of pertussis in industrialized countries despite high vaccination coverage. Current pertussis vaccines consist of antigens derived from planktonic bacterial cultures. However, recent studies have shown that biofilm formation represents an important aspect of B. pertussis infection, and antigens expressed during this stage may therefore be potential targets for vaccination. Here we provide evidence that vaccination of mice with B. pertussis biofilm-derived membrane proteins protects against infection. Subsequent proteomic analysis of the protein content of biofilm and planktonic cultures yielded 11 proteins which were ≥ three-fold more abundant in biofilms, of which Bordetella intermediate protein A (BipA) was the most abundant, surface-exposed protein. As proof of concept, mice were vaccinated with recombinantly produced BipA. Immunization significantly reduced colonization of the lungs and antibodies to BipA were found to efficiently opsonize bacteria. Finally, we confirmed that bipA is expressed during respiratory tract infection of mice, and that anti-BipA antibodies are present in the serum of convalescent whooping cough patients. Together, these data suggest that biofilm proteins and in particular BipA may be of interest for inclusion into future pertussis vaccines.Facultad de Ciencias ExactasCentro de Investigación y Desarrollo en Fermentaciones Industriale

M-protein diagnostics in multiple myeloma patients using ultra-sensitive targeted mass spectrometry and an off-the-shelf calibrator

Objectives: Minimal residual disease status in multiple myeloma is an important prognostic biomarker. Recently, personalized blood-based targeted mass spectrometry (MS-MRD) was shown to provide a sensitive and minimally invasive alternative to measure minimal residual disease. However, quantification of MS-MRD requires a unique calibrator for each patient. The use of patient-specific stable isotope labelled (SIL) peptides is relatively costly and time-consuming, thus hindering clinical implementation. Here, we introduce a simplification of MS-MRD by using an off-the-shelf calibrator. SILuMAB-based MS-MRD was performed by spiking a monoclonal stable isotope labeled IgG, Methods: SILuMAB-K1, in the patient serum. The abundance of both M-protein-specific peptides and SILuMAB-specific peptides were monitored by mass spectrometry. The relative ratio between M-protein peptides and SILuMAB peptides allowed for M-protein quantification. We assessed linearity, sensitivity and reproducibility of SILuMAB-based MS-MRD in longitudinally collected sera from the IFM-2009 clinical trial. Results: A linear dynamic range was achieved of over 5 log scales, allowing for M-protein quantification down to 0.001 » g/L. The inter-assay CV of SILuMAB-based MS-MRD was on average 11 » %. Excellent concordance between SIL- and SILuMAB-based MS-MRD was shown (R2&gt;0.985). Additionally, signal intensity of spiked SILuMAB can be used for quality control purpose to assess system performance and incomplete SILuMAB digestion can be used as quality control for sample preparation. Conclusion:Compared to SIL peptides, SILuMAB-based MS-MRD improves the reproducibility, turn-around-times and cost-efficacy of MS-MRD without diminishing its sensitivity and specificity. Furthermore, SILuMAB can be used as a MS-MRD quality control tool to monitor sample preparation efficacy and assay performance.</p