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  • Chemistry  (22)
  • 205 kDa protein  (1)
  • Hashimoto's thyroiditis
  • 1995-1999  (16)
  • 1985-1989  (8)
  • 1965-1969
  • 1
    ISSN: 1573-4919
    Keywords: MAPs ; 205 kDa protein ; Vero cells ; immunofluorescence ; cell microinjection analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Microtubule-associated proteins (MAPs) interact with tubulinin vitro andin vivo. Despite that there is a large amount of information on the roles of these proteins in neurons, the data on non-neuronal MAPs or MAPs-related proteins is scarce. There is an increasing number of microtubule-interacting proteins that have been identified in different cultured cell lines, and some of them share common functional epitopes with the most well-known MAPs, MAP-2 and tau. In a search for tubulin-interacting proteins in non-neuronal cells we identified a 205 kDa protein in the monkey kidney Vero cells in culture, on the basis of immunological studies and affinity chromatography. This protein interacts with the C-terminal moiety of β-tubulin and cosediments with taxol assembled microtubules, but it was not recovered after successive cycles of assembly and disassembly. The presence of neuronal MAPs such as MAP-1, MAP-2 and tau was not detected in these cells. Interestingly, the studies showed that the 205 kDa protein contained a tubulin binding motif which was recognized by site-directed antibodies that also tag tubulin binding epitopes on MAP-2 and tau. This characteristic led us to designate this protein as MBD-205, a component that shares binding domains with these MAPs, rather than as a marker of the MAPs family. On the other hand, immunofluorescence experiments using site-specific antibodies, i.e. MAP-reacting monoclonal anti-idiotypic reagent MTB6.22 and a polyclonal antibody to the second tau repeat, revealed a MBD-205 co-localization with membrane structures and microtubule-organizing centers in Vero cells. Microinjection studies along with studies on the cell distribution suggest that MBD-205 appears to play a structural role at the level of the microtubule interactions in these cells.
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  • 2
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Base functionalization of saturated ethylene-propylene rubbers (EPR) was performed either by means of the radical grafting of 2-(dimethylamino)ethyl methacrylate onto EPR or by the reaction of a succinic anhydride grafted EPR with N,N-dimethylethylenediamine. Differences in the structure of the grafted molecules and in their thermal stability are also reported. An investigation is made on the reactivity of EPR having tertiary amino pendant groups toward acid functionalized EPR leading to gelation.
    Additional Material: 6 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 189 (1988), S. 1207-1217 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dynamic mechanical relaxations of poly(ethylene terephthalate) (PET), poly(1,4-cyclo-hexylenedimethylene terephthalate) (PCHDMT), and a copolymer of them (COP) were measured in the temperature range from -150 to 150°C by use of a dynamic viscoelastometer. The viscoelastic relaxations of COP are studied and compared with those of PET and PCHDMT. The anisotropy of the viscoelastic properties of stretched COP samples was also studied in order to distinguish between main and secondary relaxations.
    Additional Material: 8 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 1219-1227 
    ISSN: 0887-624X
    Keywords: 1,2,4-benzenetricarboxylic acid monoesters ; poly(amide-imide) structural regularity ; poly(amide-imide) “one-pot” synthesis ; 13C-NMR spectra of poly(amide-imide) ; phosphorylation reaction ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Aromatic processable poly(amide-imide)s have been prepared according to the Yamazaki and Higashi phosphorylation reaction from flexible aromatic diamines and a mixture of isomeric 1,2,4-benzenetricarboxylic acid monoethylesters following a novel “one-pot” procedure. The polymerization was performed in 1-methyl-2-pyrrolidone/LiCl solutions using triphenylphosphite and pyridine as condensing agents to form amide bonds. Cyclization of the intermediate poly(amide-amic ethylester) occurred by eliminating ethanol under the polymerization conditions used, thus leading to the formation of imide rings. The influence of several parameters which regulate the degree of polymerization and the formation of the imide rings, such as reaction temperature, triphenylphosphite/monomers molar ratio, and pyridine concentration was carefully investigated. In particular, the catalytic activity of pyridine in the imidization reaction has been demonstrated. 13C-NMR spectroscopy has been used to show the absence of constitutional regularity in the prepared PAIs thus indicating equal reactivity toward polycondensation of the two different carboxyl groups of the 1,2,4-benzenetricarboxylic acid monoethylesters. © 1996 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 18 (1989), S. 553-557 
    ISSN: 0887-6134
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Fast atom bombardment (FAB) mass spectrometry is, for the first time, successfully applied to the underivatized anthracycline antibiotics retamycins E1 and E2, using bis-(2-hydroxyethyl)sulphide as the matrix compound. The spectra are characterized by abundant protonated molecular ions and also by a number of sequence ions, which can be easily rationalized in terms of the carbohydrate sequence in the molecules. The relative abundance of these ions seems to depend on the functionalities close to the glycosidic oxygen, and also on their stereochemical relationship. Structural results are also confirmed by the analysis of the FAB mass spectra of the acetyl derivatives.
    Additional Material: 3 Ill.
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  • 6
    ISSN: 0935-9648
    Keywords: 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
    Additional Material: 4 Ill.
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  • 7
    ISSN: 0935-9648
    Keywords: 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
    Additional Material: 5 Ill.
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  • 8
    ISSN: 0899-0042
    Keywords: Circular dichroism ; helicity rule ; X-ray structure determination ; ultraviolet spectra ; n - π* and π - π* bands ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chiroptical properties of a series of 3 and/or 4-heterosubstituted 2(5H)-furanones were investigated with respect to correlation with absolute configuration. The n - π* and π - π* Cotton effects have been assigned on the basis of comparison with the UV spectra in solvents of varying polarity. It is demonstrated that the n - π* transition in 4-amino substituted 2(5H)-furanones appears at shorter wavelength with respect to the π - π* transition. With the exception of 4-pyrrolidino and 4-benzylamino substituted 2(5H)-furanones, other heterosubstituted 2(5H)-furanones follow the butenolide configurational rule (Gawronski et al. J. Org. Chem. 61:1513-1515, 1996). Absolute configuration of 2(5H)-furanone derivatives can also be assigned according to the sign of the Cotton effect (of unknown origin) at 200-230 nm. The structure of four representative sulfur and nitrogen substituted 2(5H)-furanones has been analyzed by X-ray diffraction. The results indicate planarity of the furanone ring and extended conjugation in 4-amino substituted 2(5H)-furanones. Chirality 9:537-544, 1997. © 1997 Wiley-Liss, Inc.
    Additional Material: 4 Ill.
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  • 9
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Kinetik der Vulkanisation sowie die Vernetzungsdichte von Styrol-Butadien-Kautschukmischungen wurden mit zwei Vulkanisationssystemen, einem wirksamen (EV) und einem konventionellen (CV), untersucht. Ein oberflächenmodifiziertes Silikat mit Boramingruppen (Si—O—B—(NH2)2) wurde als Füllstoff eingesetzt. Unbehandeltes und mit zwei Silanen (γ-Mercaptopropyl-trimethoxysilan und γ-Aminopropyl-triethoxysilan) modifiziertes Silikat wurden zum Vergleich eingesetzt. Die bestenkinetischen Parameter, wie die höchste Vulkanisierungsgeschwindigkeit, die längste Induktionszeit und die kleinste Aktivierungsenergie, wurden für die Mischung mit boraminiertem Silikat erhalten. Die Vernetzungsdichte, die mit dieser Mischung erreicht wurde, ist ähnlich der von mit Silan modifiziertem Silikat erzielten, da wahrscheinlich die Boramingruppen auf der Silikatoberfläche besser verteilt sind. Diese Fakten führen zu wichtigen technologischen Verbesserungen: größere Verarbeitungssicherheit, schnellere Vulkanisierungsgeschwindigkeit und verbesserte physikalische Eigenschaften.
    Notes: Vulcanization kinetics and crosslink density of styrene-butadiene rubber compounds have been studied with two vulcanization systems, an efficient (EV) and a conventional (CV) one. A surface-modified silica with boron-amine groups (Si—O—B—(NH2)2) was employed as filler. Untreated and modified silica with two silanes (γ-mercaptopropyl-trimethoxysilane and γ-aminopropyl-triethoxysilane) have been used as reference.The best kinetic parameters, such as highest vulcanization rate, longest induction time and lowest activation energy, were obtained for the compound with boronaminated silica. The crosslink density, achieved with this compound, is similar to that with silane-modified silica, probably because of the better surface distribution of boron-amine groups on the silica. These facts lead to important technological improvements: better processing safety, faster vulcanization rate and improved physical properties.
    Additional Material: 4 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Bioluminescence and Chemiluminescence 13 (1998), S. 371-378 
    ISSN: 0884-3996
    Keywords: bioluminescence ; luciferase ; ATP ; immobilization ; glass ; poly-L-lysine ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: The bioluminescent reaction catalysed by firefly luciferase has become widely established as an outstanding analytical system for assay of ATP. When used in solution, luciferase is unstable and cannot be re-used, a problem that can be partially circumvented by immobilizing the enzyme on solid substrates. Transparent glass is especially advantageous over alternative immobilizing matrices, since it allows most of the emitted photons to be detected. We report a new method for luciferase immobilization on glass which does not require prior silanization and glutaraldehyde activation, thus saving preparation time and minimizing enzyme inactivation. Our method is based on the co-immobilization by adsorption of luciferase (from a firefly lantern extract) and poly-L-lysine (PL) on non-porous glass strips. Luciferase immobilized in this way exhibits minimal variations in intersample activity, high sensitivity for ATP detection (linear luminescence responses down to 50 nmol/L) and good stability (full activity for at least 60 days when stored at -80°C). PL-mediated immobilization of luciferase on glass strips provides an attractive strategy for the design of specific ATP biosensors, with potential in industry, environmental screening, medicine and biological research. © 1998 John Wiley & Sons, Ltd.
    Additional Material: 3 Ill.
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