65 research outputs found

    grofit: Fitting Biological Growth Curves with R

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    The grofit package was developed to fit many growth curves obtained under different conditions in order to derive a conclusive dose-response curve, for instance for a compound that potentially affects growth. grofit fits data to different parametric models and in addition provides a model free spline method to circumvent systematic errors that might occur within application of parametric methods. This amendment increases the reliability of the characteristic parameters (e.g.,lag phase, maximal growth rate, stationary phase) derived from a single growth curve. By relating obtained parameters to the respective condition (e.g.,concentration of a compound) a dose response curve can be derived that enables the calculation of descriptive pharma-/toxicological values like half maximum effective concentration (EC50). Bootstrap and cross-validation techniques are used for estimating confidence intervals of all derived parameters.

    Aufbau eines pharma-/toxikologischen Testsystems für die Säuger-Kaliumkanäle <em>mKir2.1</em> und hERG mit Hilfe des Modellorganismus <i>Saccharomyces cerevisiae</i>

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    Die humanen Kaliumkanäle hERG und Kir2.1 tragen wesentlich zur Repolarisierung des kardialen Membranpotentials bei (Sanguinetti et al., 1995; Wible et al., 1995). Fehlfunktionen in diesen Kanälen können zu einer Verzögerung der kardialen Repolarisation, einer Verlängerung des QT-Intervalls im Oberflächen-EKG und zu lebensbedrohlichen Herzrhythmusstörungen führen (Tristani-Firouzi et al., 2002; Sanguinetti & Tristani-Firouzi, 2006). Ziel der Arbeit war die Charakterisierung von hERG und dem zum humanen Kir2.1-Protein orthologen Kir2.1-Protein aus der Maus in Saccharomyces cerevisiae K+-Transportmutanten. Die funktionelle Expression von chromosomal als auch episomal exprimierter mKir2.1-cDNA komplementierte den mutanten Wachstumsphänotyp unter nicht permissiven Bedingungen (3-10 mM KCl) in Abhängigkeit vom externen pH. GFP-mKir2.1 Fusionsproteine konnten in der Plasmamembran oder zumindest in unmittelbarer Nähe zu dieser lokalisiert werden. Unter nicht permissiven (20 mM KCl) wie auch permissiven Bedingungen (100 mM KCl) zeigten mKir2.1 exprimierende Zellen, verglichen mit einem Kontrollstamm ohne mKir2.1, eine deutlich verringerte Sensitivität gegenüber dem als Indikator für das Membranpotential beschriebenen Antibiotikum Hygromycin B, was auf eine Membrandepolarisierung mit funktionellem mKir2.1 hindeutet. Die Untersuchung des Wachstums von mKir2.1 exprimierenden Stämmen bei Zugabe der bekannten Blocker von Kir2.1 Ag+, Cs+, Ba2+ und 48F10 zeigte unter K+-limitierenden Bedingungen eine signifikante Inhibierung von mKir2.1 spezifischem Wachstum. Im Zuge der Entwicklung eines standardisierten Testsystems zur Durchmusterung von potentiellen Modulatoren von Kir2.1 wurde in einem Ringtest die Übertragbarkeit dieser Wachstumstests auf andere Labore am Beispiel eines standardisierten CsCl-Test untersucht und bestätigt. Unter permissiven Bedingungen (≥ 50 mM KCl) und pH 7 führte darüber hinaus die Expression von mKir2.1 zu einer signifikanten Wachstumsinhibierung und damit zu einem weiteren mKir2.1 spezifischen Phänotyp. Diese Wachstumsinhibierung konnte durch Zugabe von CsCl und in K+-Effluxmutanten durch Zugabe von BaCl2 aufgehoben werden. Damit konnte für diesen K+-Kanal die funktionelle heterologe Expression gezeigt werden und es wurden zwei neue, bisher nicht beschriebene Phänotypen identifiziert. Mit den konstruierten Hefestämmen steht ein pharma-/toxikologisches Testsystem zur Verfügung, für das die Sensitivität, Spezifität und der Vergleich mit dem ‚Gold Standard’ unter standardisierten Bedingungen gezeigt werden konnte. Die Expression von HERG-cDNA führte in S. cerevisiae K+-Aufnahmemutanten zu keiner Komplementation des mutanten Wachstumsphänotyps. Bei der Expression von Fusionskonstrukten aus GFP und HERG konnte keine Lokalisation an der Zelloberfläche beobachtet werden. Auch die Konstruktion verschiedener HERG-Modifikationen im Sinne eines verbesserten Membran- ‚Targeting’ und/oder verbessertem ER-Exports konnten keine Lokalisierung in oder in der Nähe der Plasmamembran sowie keine erfolgreiche Komplementation bewirken

    Towards Immersive Telepresence SCHLOSSTAG’97

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    Today’s technology and advances in networking and multimedia systems stimulate a change in the way business is carried out, making it a globally distributed process, in which communication and collaboration of geographically dispersed group is of vital importance. Teleconferencing and collaborative telepresence systems that provide high-degree of copresence give enough evidences that projective VR systems when combined with multimedia facilities, such as real-time video and audio, can greatly facilitate the communication and collaboration over distance in a variety of application areas. The approach presented in this paper, creates an environment where remote participants not only meet as if face to face, but also share the same virtual space and perform common tasks. Multimedia datastreams, such as live stereo-video and audio, from a projective VR system are transmitted and integrated into the virtual space of another participant at a distant VR system, allowing geographically separated groups to meet in a common virtual space, while maintaining eyecontact, gaze awareness and body language

    Analysis of the mKir2.1 channel activity in potassium influx defective Saccharomyces cerevisiae strains determined as changes in growth characteristics

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    AbstractPotassium uptake defective Saccharomyces cerevisiae strains (Δtrk1,2 and Δtrk1,2 Δtok1) were used for the phenotypic analysis of the mouse inward rectifying Kir2.1 channel by growth analysis. Functional expression of both, multi-copy plasmid and chromosomally expressed GFP-mKir2.1 fusion constructs complemented the potassium uptake deficient phenotype in a pHout dependent manner. Upon application of Hygromycin B to chromosomally mKir2.1 expressing cells, significantly lower toxin sensitivity (EC50 15.4μM) compared to Δtrk1,2 Δtok1 cells (EC50 2.6μM) was observed. Growth determination of mKir2.1 expressing strains upon application of Ag+, Cs+ and Ba2+ as known blockers of mKir2.1 channels revealed significantly decreased channel function. Cells with mKir2.1 were about double sensitive to AgNO3, 350-fold more sensitive to CsCl and 1500-fold more sensitive to BaCl2 in comparison to the respective controls indicating functional expression and correct pharmacology

    Association of serum sex steroid receptor bioactivity and sex steroid hormones with breast cancer risk in postmenopausal women

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    Postmenopausal women with elevated serum sex steroids have an increased risk of breast cancer. Most of this risk is believed to be exerted through binding of the sex steroids to their receptors. For the first time, we investigate the association of estrogen receptor (ER) and androgen receptor (AR) serum bioactivity (SB) in addition to hormone levels in samples from women with breast cancer collected before diagnosis. Two hundred postmenopausal women participating in the UK Collaborative Trial of Ovarian Cancer Screening who developed ER-positive breast cancer 0.6–5 years after sample donation were identified and matched to 400 controls. ER and AR bioassays were used to measure ERα, ERβ, and AR SB. Androgen and estrogen levels were measured with immunoassays. Subjects were classified according to quintiles of the respective marker among controls and the associations between SB and hormones with breast cancer risk were determined by logistic regression analysis. ERα and ERβ SB were significantly higher before diagnosis compared with controls, while estrogens showed no difference. Women had a twofold increased breast cancer risk if ERα SB (odds ratio (OR), 2.114; 95% confidence interval (CI), 1.050–4.425; P=0.040) was in the top quintile >2 years before diagnosis or estrone (OR, 2.205; 95% CI, 1.104–4.586; P=0.029) was in the top quintile <2 years before diagnosis. AR showed no significant association with breast cancer while androstenedione (OR, 3.187; 95% CI, 1.738–6.044; P=0.0003) and testosterone (OR, 2.145; 95% CI, 1.256–3.712; P=0.006) were significantly higher compared with controls and showed a strong association with an almost threefold increased breast cancer risk independent of time to diagnosis. This study provides further evidence on the association of androgens and estrogens with breast cancer. In addition, it reports that high ER but not AR SB is associated with increased breast risk >2 years before diagnosis

    Epigenotyping in Peripheral Blood Cell DNA and Breast Cancer Risk: A Proof of Principle Study

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    Background: Epigenetic changes are emerging as one of the most important events in carcinogenesis. Two alterations in the pattern of DNA methylation in breast cancer (BC) have been previously reported; active estrogen receptor-a (ER-a) is associated with decreased methylation of ER-a target (ERT) genes, and polycomb group target (PCGT) genes are more likely than other genes to have promoter DNA hypermethylation in cancer. However, whether DNA methylation in normal unrelated cells is associated with BC risk and whether these imprints can be related to factors which can be modified by the environment, is unclear.Methodology/Principal Findings: Using quantitative methylation analysis in a case-control study (n = 1,083) we found that DNA methylation of peripheral blood cell DNA provides good prediction of BC risk. We also report that invasive ductal and invasive lobular BC is characterized by two different sets of genes, the latter particular by genes involved in the differentiation of the mesenchyme (PITX2, TITF1, GDNF and MYOD1). Finally we demonstrate that only ERT genes predict ER positive BC; lack of peripheral blood cell DNA methylation of ZNF217 predicted BC independent of age and family history (odds ratio 1.49; 95% confidence interval 1.12-1.97; P = 0.006) and was associated with ER-a bioactivity in the corresponding serum.Conclusion/Significance: This first large-scale epigenotyping study demonstrates that DNA methylation may serve as a link between the environment and the genome. Factors that can be modulated by the environment (like estrogens) leave an imprint in the DNA of cells that are unrelated to the target organ and indicate the predisposition to develop a cancer. Further research will need to demonstrate whether DNA methylation profiles will be able to serve as a new tool to predict the risk of developing chronic diseases with sufficient accuracy to guide preventive measures

    HIV-1 Vpu Protein Mediates the Transport of Potassium in Saccharomyces cerevisiae

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    Human immunodeficiency virus type 1 (HIV-1) Vpu is an integral membrane protein that belongs to the viroporin family. Viroporins interact with cell membranes, triggering membrane permeabilization and promoting release of viral particles. In vitro electrophysiological methods have revealed changes in membrane ion currents when Vpu is present; however, in vivo the molecular mechanism of Vpu at the plasma membrane is still uncertain. We used the yeast Saccharomyces cerevisiae as a genetic model system to analyze how Vpu ion channel impacts cellular homeostasis. Inducible expression of Vpu impaired cell growth, suggesting that this viral protein is toxic to yeast cultures. This toxicity decreased with extracellular acidic pH. Also, Vpu toxicity diminished as the extracellular K(+) concentration was increased. However, expression of the Vpu protein suppresses the growth defect of K(+) uptake-deficient yeast (Δtrk1,2). The phenotype rescue of these highly hyperpolarized cells was almost total when they were grown in medium supplemented with high concentrations of KCl (100 mM) at pH 7.0 but was significantly reduced when the extracellular K(+) concentration or pH was decreased. These results indicate that Vpu has the ability to modify K(+) transport in both yeast strains. Here, we show also that Vpu confers tolerance to the aminoglycoside antibiotic hygromycin B in Δtrk1,2 yeast. Our results suggest that Vpu interferes with cell growth of wild-type yeast but improves proliferation of the hyperpolarized trk1,2 mutant by inducing plasma membrane depolarization. Furthermore, evaluation of the ion channel activity of the Vpu protein in Δtrk1,2 yeast could aid in the development of a high-throughput screening assay for molecules that target the retroviral protein.This study was supported by Grants PI PI05/00013 and PI08/0912 from Fondo de Investigación Sanitaria. L.H. and N.M. were holders of Predoctoral Fellowships from Instituto de Salud Carlos III.S

    Endocytic regulation of alkali metal transport proteins in mammals, yeast and plants

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    The relative concentrations of ions and solutes inside cells are actively maintained by several classes of transport proteins, in many cases against their concentration gradient. These transport processes, which consume a large portion of cellular energy, must be constantly regulated. Many structurally distinct families of channels, carriers, and pumps have been characterized in considerable detail during the past decades and defects in the function of some of these proteins have been linked to a growing list of human diseases. The dynamic regulation of the transport proteins present at the cell surface is vital for both normal cellular function and for the successful adaptation to changing environments. The composition of proteins present at the cell surface is controlled on both the transcriptional and post-translational level. Post-translational regulation involves highly conserved mechanisms of phosphorylation- and ubiquitylation-dependent signal transduction routes used to modify the cohort of receptors and transport proteins present under any given circumstances. In this review, we will summarize what is currently known about one facet of this regulatory process: the endocytic regulation of alkali metal transport proteins. The physiological relevance, major contributors, parallels and missing pieces of the puzzle in mammals, yeast and plants will be discussed.This work was supported by grant BFU2011-30197-C03-03 from the Ministerio de Ciencia e Innovacion (Spain). V.L.-T. is supported by a fellowship from the Universidad Politecnica de Valencia. C. P. is supported by a fellowship from the Consejo Superior de Investigaciones Cientificas (Spain).Mulet Salort, JM.; Llopis Torregrosa, V.; Primo Planta, C.; Marques Romero, MC.; Yenush, L. (2013). 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