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  • Cell & Developmental Biology  (8)
  • General Chemistry  (8)
  • Polymer and Materials Science  (3)
  • 11
    ISSN: 0935-9648
    Keywords: Sensors ; ISFETs and CHEMFETs ; Polysiloxanes ; Reference FETs ; Polymer Membranes ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Synthetic receptor molecules that selectively bind charged guests can store chemical information. The transduction of this information into electronic signals connects the chemical and electronic domains. Field effect transistors (FETs) are attractive transducing elements because these microdevices are able to register and amplify chemical changes at the gate oxide surface of the semiconductor chip.Integration of molecular receptors and field effect transistors into one chemical system gives a device that can communicate-changes of substrate activities in aqueous solution. Simulations of a system in which the receptor molecules are directly attached to the FET gate oxide indicate serious limitations with respect to sensitivity, dynamic range and extreme requirements for complex stability. Therefore we have concentrated on the integration of covalently attached thin membranes.The problem of the thermodynamically ill-defined oxidemembrane ipterface has been solved by applying a covalently linked hydrophilic polyhydroxyethylmethacrylate (polyHEMA) gel between the sensing membrane and the silylated gate oxide. A buffered aqueous electrolyte solution in the hydrogel renders the surface potential at the gate oxide constant via the dissociation equilibrium of the residual silanol groups. The subsequent attachment of a polysiloxane membrane that has the required dielectric constant, glass transition temperature Tg, and receptor molecule, provides a stable chemical system that transduces the complexation of cationic species into electronic signals (CHEMFET).The response to changing K⊕ concentrations in a solution of 0.1 M NaCl is fast (〈1 sec) and linear in the concentration range of 10-5-1.0 M (55-58 mV /decade). A reference FET (REFET) based on the same technology is obtained when the intrinsic sensitivity to changes in ion concentration is eliminated by the addition of 2.10-5 mol g-1 of didodecyldimethyl ammonium bromide to the ACE membrane. Differential measurements with a REFET/CHEMFET combination showed excellent linear K⊕ response over long periods of time.All chemical reactions used are compatible with planar IC technology and allow fabrication on wafer scale.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 82 (1942), S. 255-259 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 124 (1985), S. 1-8 
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The relationship between lipoproteins and growth of aortic smooth muscle cells has been a matter of controversy. We therefore reexamined this issue using serum-free defined media methodology. By themselves, LDL or HDL (50-500 μg/ml) from normolipemic human or bovine plasma produced little or no growth of homologous aortic smooth muscle cells incubated in serumfree medium that was supplemented with insulin and transferrin to maintain cell viability. In fact, LDL prepared in the absence of an antioxidant (BHT) was toxic to these cells. However, in the presence of maximally effective concentrations of platelet-derived growth factor (PDGF), LDL or HDL consistently increased the growth of homologous smooth muscle cells (up to twofold increases in DNA accumulation in 48 hr). Lipoproteins also augmented the growth response of arterial smooth muscle cells to fibroblast growth factor or epidermal growth factor. The mechanism of this effect was investigated further with HDL, because, in contrast to LDL, HDL apoproteins are water-soluble. Neither HDL delipidated by solvent extraction (apoHDL), purified bovine apoA-I, nor cholesterol added in the form of phospholipid vesicles appreciably increased PDGF-induced growth of bovine smooth muscle cells. However, HDL-like particles reconstituted by sonication of apoHDL with cholesterol and phospholipids did increase the growth of cultures of bovine smooth muscle cells treated with PDGF. Uptake of tritiated thymidine by cultures incubated with partially purified PDGF alone (10 μg/ml) was 5,693 ± 235 dpm/24 hr compared to 10,381 ± 645 dpm/24 hr (p 〈 0.01) in the presence of both PDGF and reconstituted HDL-like particles (250 μg protein/ml). Thus both the lipid and protein components of HDL may be necessary for optimal potentiation of growth of mitogen-stimulated cells. These results indicate that lipoproteins from normolipemic sera are not bona fide growth factors but can potentiate the growth of mitogen-stimulated cells, perhaps by supplying exogenous cholesterol required for membrane biogenesis. This finding might be important in arterial injury when the release of PDGF and exposure to plasma lipoproteins could act in concert to stimulate the proliferation of smooth muscle cells.
    Additional Material: 5 Ill.
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  • 14
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 92 (1980), S. 429-444 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Glykogen-Phosphorylasen katalysieren den Abbau von Glykogen durch Phosphat (oder Arsenat) zu Glucose-1-phosphat (bzw. Glucose + Arsenat). Alle Glykogen-Phosphorylasen enthalten Pyridoxal-5′-phosphat, ein Vitamin-B6-Derivat, als Cofaktor. Es ist im Enzym durch eine Doppelbindung mit der ∊-Aminogruppe eines Lysinrestes verbunden. Wird der Cofaktor vom Enzymprotein abgetrennt, erhält man inaktives Apoenzym. Das Enzym bleibt jedoch aktiv, wenn man die Doppelbindung mit NaBH4 reduziert. Sollte daher Pyridoxalphosphat an der Katalyse der Glykogen-Phosphorylasen beteiligt sein, so müßte es eine andere Funktion als in allen anderen „klassischen“ Pyridoxalphosphat-abhängigen Enzymen haben, denn diese werden durch Reduktion inaktiviert. Die 31P-NMR-Spektroskopie hat gezeigt, daß die Phosphatgruppe von Pyridoxalphosphat in den katalytisch aktiven Formen der Glykogen-Phosphorylasen als Dianion in einer hydrophoben Umgebung vorliegt. Die kovalente und allosterische Aktivierung der Muskel-Glykogen-Phosphorylasen wird von der Umwandlung der monoprotonierten Form der Phosphatgruppe des Cofaktors in die dianionische Form begleitet. Wir fanden nun derartige Ionisierungsänderungen auch bei den nichtregulierten aktiven Kartoffel- und E. -coli-Maltodextrin-Phosphorylasen, und zwar bei der Bindung von Glucose und Oligosacchariden sowie bei katalytischem Umsatz, d. h. Arsenolyse der α-1,4-glykosidischen Bindungen. (Maltodextrin-Phosphorylasen gehören wie Glykogen-Phosphorylasen zur Klasse der α-Glucan-Phosphorylasen.) Versuche unserer Gruppe sowie neuere Befunde über die Raumstruktur der kristallinen Muskel-Glykogen-Phosphorylase legen es nahe, die dianionische Phosphatgruppe als Protonenacceptor beim Glucosyltransfer vom und zum Glucosylacceptor anzusehen. Wenn dies auch nicht die einzige Erklärung der Befunde sein mag, so kann doch nicht mehr daran gezweifelt werden, daß die dianionische Phosphatgruppe des Cofaktors der Glykogen-Phosphorylasen eine katalytische Funktion ausübt.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 15
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 95 (1983), S. 336-337 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 16
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    BioEssays 17 (1995), S. 287-290 
    ISSN: 0265-9247
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Ethylene (C2H4) is a gaseous plant hormone produced by higher and lower (green) plants and, when grown on appropriate substrates, also by fungi, yeasts and bacteria. Ethylene is involved in many developmental processes in plants and is biologically active in trace amounts (10 - 100 nl/I of air) that may be present in the outside air due to industrial air pollution(1). Fruit ripening and flower senescence especially, in a variety of commercially important crops, are dramatically stimulated by ethylene. Following characterization of the genes coding for the key enzymes in ethylene biosynthesis, i.e. ACC synthase and ACC oxidase, it has become clear that their expression is regulated in a complex manner involving developmental, hormonal and tissue-specific factors. This was recently very elegantly demonstrated for the expression of ACC oxidase genes in developing petunia flowers by Tang et al.(2). The spatial and temporal expression patterns, especially in the reproductive organs, suggest a hitherto unknown role for ethylene in reproductive processes such as the self-incompatible response and the secretion of cellular exudate by the stigma and nectary.
    Additional Material: 1 Ill.
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  • 17
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 17 (1978), S. 541-541 
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 18
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 19 (1980), S. 441-455 
    ISSN: 0570-0833
    Keywords: Pyridoxal phosphate ; Enzyme catalysis ; Glycogen phosphorylases ; Phosphorylases ; Enzymes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Glycogen phosphorylases catalyze the degradation of glycogen by phosphate (or arsenate) to glucose 1-phosphate (or glucose + arsenate). All glycogen phosphorylases that have been studied so far contain pyridoxal 5′-phosphate, a vitamin B6-derivative, as cofactor. Removal of the cofactor results in an inactive apoenzyme. However, reduction of the azomethine bond linking pyridoxal phosphate to an ε-aminolysyl side chain of the enzyme with NaBH4 does not inactivate glycogen phosphorylase. If therefore the cofactor should be involved in catalysis in glycogen phosphorylase it must function differently from all other classical pyridoxal phosphate dependent enzymes, for these are inactivated by reduction. 31P-NMR spectroscopy has revealed that the 5′-phosphate group of pyridoxal phosphate is present in catalytically active forms of glycogen phosphorylases as dianion in a hydrophobic environment shielded from aqueous solvent. Covalent and/or allosteric activation of muscle glycogen phosphorylases is accompanied by a transition of the monoprotonated form to the dianionic form of the phosphate group of the cofactor. We now report on such ionization changes in unregulated active potato- and E. coli maltodextrin phosphorylases on binding of glucose and oligosaccharides and following catalytic turnover, i.e. arsenolysis of α-1,4-glycosidic bonds. (Like glycogen phosphorylases, maltodextrin phosphorylases belong to the class of α-glucan phosphorylases.) The results of experiments carried out by our group together with recent findings on the three dimensional structure of crystalline muscle glycogen phosphorylases indicate a participation of the dianionic phosphate group as proton acceptor for the glucosyl transfer to and from the glucosyl acceptor. Although other interpretations are not excluded, at present little doubt remains that in the case of glycogen phosphorylases the dianionic phosphate group of the cofactor functions in catalysis.
    Additional Material: 12 Ill.
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  • 19
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 22 (1983), S. 168-170 
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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