Über Beziehungen der Kernä Quivalente von Schizophyten zu den Mitochondrien höher organisierter Zellen

Zusammenfassung In den Zellzentren von Schizophyten können außer Desoxyribonukleinsäure — die den kernäquivalenten Charakter der Organelle begründet — Ribonukleinsäure, Phosphate und Lipoide nachgewiesen werden. Das Vorhandensein dieser Stoffgruppen macht Beziehungen der Zellzentren zu den Mitochondrien höher organisierter Zellen wahrscheinlich. Desoxyribonukleinsäurekomplexe der Kernäquivalente und Phosphatkörper der Mitochondrienäquivalente haben — obwohl Komponenteneines Organells — eine gesonderte ontogenetische Entwicklung.Der gemeinsame Ursprung der phylogenetischen Entwicklung von Zellkern und Mitochondrien bzw. von diesen ableitbaren Zellorganellen (Plastiden) wird als möglich angesehen. Die Rolle dieser Organelle als Organisationszentren erscheint durch die aufgezeigten Zusammenhänge unter neuen Gesichtspunkten.Mit 2 Textabbildungen.     

Evaluation of SYPRO Ruby total protein stain for the normalization of two-dimensional Western blots

Due to post-translational modifications such as phosphorylation, proteins exist as distinct charge variants. Two-dimensional (2D) gel electrophoresis followed by immunoblotting enables the detection of these isoforms. For their accurate relative quantitation in different samples, a loading control is necessary to compensate for technical errors such as imprecise sample loading or transfer. The study reveals that the combinatory approach of SYPRO Ruby and chemiluminescence-based 2D Western blot analysis exhibits high linearity and excellent reproducibility and is applicable for limited sample amounts.     

Control of the bifunctional O2-sensor kinase NreB of Staphylococcus carnosus by the nitrate sensor NreA: Switching from kinase to phosphatase state

The NreB–NreC two-component system of Staphylococcus carnosus for O₂ sensing cooperates with the accessory nitrate sensor NreA in the NreA–NreB–NreC system for coordinated sensing and regulation of nitrate respiration by O₂ and nitrate. ApoNreA (NreA in the absence of nitrate) interacts with NreB and inhibits NreB autophosphorylation (and activation). NreB contains the phosphatase motif DxxxQ. The present study shows that NreB on its own was inactive for the dephosphorylation of the phosphorylated response regulator NreC (NreC-P), but co-incubation with NreB and NreA stimulated NreC-P dephosphorylation. Either the presence of instead of apoNreA or mutation of the phosphatase motif (D160 or Q164) of NreB abrogated phosphatase activity of NreB. Phosphatase activity was observed for anoxic (active) NreB as well as oxic NreB, therefore the functional state of NreB is not relevant for phosphatase activity. Thus, NreB is a bifunctional sensor kinase with an integral cryptic phosphatase activity. Activation of phosphatase activity and dephosphorylation of NreC-P requires NreA as a cofactor. Accordingly, NreA and nitrate have major and dual roles in NreA–NreB–NreC regulation by (i) inhibiting NreB phosphorylation and (ii) triggering a kinase/phosphatase switch of NreB when present as apoNreA.     

HIV-1 testing: product development strategies.

Strategies for the development of diagnostic products for acquired immune deficiency syndrome (AIDS) are inextricably linked to the status of our knowledge of the human immunodeficiency virus (HIV) and the events associated with the pathogenesis of AIDS. This review traces product development strategies from 1984 to the present day. Product development activities in the HIV-1 antibody screening test market were a response to the need to remove contaminated units from the blood supply. With the successes in screening blood and blood products, there has been a shift towards product development for personal health care and applicant suitability. Identification of markers for disease progression and the need to monitor therapeutic efficacy is now leading to tests for patient disease staging, monitoring and prognosis.     

Yaw stability in gliding birds

A new concept for describing the yaw stability in gliding birds is presented. This concept introduces dynamic stiffness in yaw as an appropriate indication of stability. Other than the conventional metric of static yaw stability given by the gradient of the aerodynamic yawing moment with respect to the sideslip angle, the dynamic stiffness does not only provide a qualitative indication of stability but also a precise quantitative measure of the restoring action in the yaw axis. With the use of scaling relations, it is shown that the dynamic stiffness of birds is sufficiently high though their static yaw stability may be very small. The underlying mechanism is that the yaw moment of inertia is more reduced with a decrease in size than the restoring aerodynamic moment. Reference is made to the yaw stability in aircraft and related flying qualities requirements. Thus, numerical values are derived which can be used as a standard of comparison providing a rating basis for the dynamic yaw stiffness in small flying objects, like birds. Furthermore, it is shown that the wings of birds produce yawing moments due to sideslip so large that a sufficiently high level of dynamic yaw stiffness can be achieved. From the results derived in this paper, it may be concluded that birds—unlike aircraft—need no vertical tail for yaw stability.     

Comparative anticholinergic potencies of R- and S- disopyramide in longitudinal muscle strips from guinea pig ileum

The anticholinergic potencies of R- and S- disopyramide were studied in isolated myenteric plexus longitudinal muscle strip preparations from guinea-pig ileum using two experimental procedures. The first procedure tested the relative potencies of the isomers in inhibiting electrically-stimulated contractions in 6 ileum preparations. A balanced crossover design was employed. The mean concentration of S-disopyramide required to inhibit electrically stimulated contractions by 50% was 4.6 × 10^?6 M and was about one-fourth of the concentration of R-disopyramide required to produce the same effect (p < 0.05). The second procedure tested the relative potencies of the isomers as direct antagonists of contractions induced by either histamine or acetylcholine in ileum preparations. Neither isomer antagonized the histamine-induced contractions. For the contractions induced by acetylcholine, the pA₂ value, obtained directly from Schild plots, was 6.25 for S- and 5.74 for R- disopyramide. However, the slope of the Schild plot for the S-isomer differed significantly from ?1, suggesting that other mechanisms in addition to direct antagonism of acetylcholine may be involved. Thus, the results of the experiments involving both the antagonism of electrically stimulated contractions and the direct antagonism of acetylcholine-induced contractions indicate (1) that both isomers of disopyramide have anticholinergic properties and (2) that S-disopyramide is about 3–4 fold more potent as an anticholinergic agent.     

Identification of Rabbit Oviductal Fluid Proteins Involved in Pre‐Fertilization Processes by Quantitative Proteomics

Oviductal fluid (ODF) proteins modulate and support reproductive processes in the oviduct. In the present study, proteins involved in the biological events that precede fertilization have been identified in the rabbit ODF proteome, isolated from the ampulla and isthmus of the oviduct at different time points within 8 h after intrauterine insemination. A workflow is used that integrates lectin affinity capture with stable‐isotope dimethyl labeling prior to nanoLC‐MS/MS analysis. In total, over 400 ODF proteins, including 214 lectin enriched glycoproteins, are identified and quantified. Selected data are validated by Western blot analysis. Spatiotemporal alterations in the abundance of ODF proteins in response to insemination are detected by global analysis. A subset of 63 potentially biologically relevant ODF proteins is identified, including extracellular matrix components, chaperones, oxidoreductases, and immunity proteins. Functional enrichment analysis reveals an altered peptidase regulator activity upon insemination. In addition to protein identification and abundance changes, N‐glycopeptide analysis further identifies 281 glycosites on 199 proteins. Taken together, these results show, for the first time, the evolving oviductal milieu early upon insemination. The identified proteins are likely those that modulate in vitro processes, including spermatozoa function.