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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 15 (1990), S. 156-161 
    ISSN: 0886-1544
    Keywords: microtubule structure ; microtubule assembly ; electron microscopy of microtubules ; polymer stabilization ; microtubule-capping structures ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Microtubules contain in their lumens distinct structures (plugs) that influence their dynamic behavior in vitro. As observed by electron microscopy, plugs are stainoccluding structures 10-30 nm in length that occur along the lengths and at the ends of microtubules. Plugs occur at a frequency of 20-40% at the ends of microtubules assembled from cycled microtubule protein containing MAPs. While the composition of plugs is not known, preliminary evidence suggests that they are accretions of tubulin, that they are labile, and that they are more common in preparations containing MAPs. When polymers are induced to depolymerize by endwise subuit dissociation, the frequency of plugged microtubule ends increases transiently, suggesting that plugs temporarily stabilize microtubules. The functional significance of plugs may be that they prevent the sudden complete loss of microtubules through catastrophic disassembly. It is possible that plugs, by slowing the rate of disassembly, enable a polymer to add GTP-tubulin subunits, thereby forming a stabilizing GTP-cap. These observations suggest that plugs may stabilize polymers and account for the frequent transitions from shortening to growing phases that characterize dynamic instability.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Biomaterials 1 (1990), S. 333-333 
    ISSN: 1045-4861
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Biomaterials 2 (1991), S. 61-62 
    ISSN: 1045-4861
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Biomaterials 1 (1990), S. 95-97 
    ISSN: 1045-4861
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Biomaterials 3 (1992), S. 165-165 
    ISSN: 1045-4861
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Biomaterials 1 (1990), S. 259-261 
    ISSN: 1045-4861
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Previous studies have shown that the B/E (low density lipoprotein [LDL]) receptor pathway plays a minor role in cholesterol uptake in the intact rat ovary, but when granulosa cells are isolated and maintained in culture, the cells develop a fully functional B/E receptor system. In the current study we examined the development of the B/E receptor over time (96 h) in culture and compared its physiological function, expression of mRNA and protein levels, and morphological events to the upregulation induced in 24 h by hormone (human chorionic gonadotropin [hCG] or Bt2cAMP). With both protocols, increased progestin production occurs and is associated with elevated binding, uptake, and degradation of LDL in the medium although the impact of Bt2cAMP stimulation on all these measurements is several times that observed with time alone. Only the hormone-stimulated LDL receptor response was associated with an increase in receptor protein (Western blot) or mRNA levels (RNase protection assay). We conclude that unstimulated granulosa cells show posttranslational increase in B/E receptor activity with time in culture, but transcriptional changes in B/E receptor follow stimulation with trophic hormone or its second messenger, cAMP. © 1994 Wiley-Liss, Inc.
    Additional Material: 11 Ill.
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  • 8
    ISSN: 0749-1581
    Keywords: Schiff bases ; Tautomerism ; 13C NMR CP/MAS ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13C and 1H NMR spectra of six Schiff bases formed from 2-hydroxy-1-naphthaldehyde and substituted anilines were measured and assigned in a variety of solvents. Based on the 13C chemical shifts and 3J(CH,NH), the ratio of the keto-amine and phenol-imine tautomers was derived using both 13C chemical shifts and 1H-1H coupling constants, the two methods giving comparable results. The solid-state 13C NMR spectra of two of these Schiff bases were also measured and interpreted. Based on chemical shift assignments from solution NMR, which showed a relationship between certain shifts and the proportions of the tautomers, it has been shown that these compounds exist essentially as the keto-amine form in the solid, the tautomer previously shown to be the more thermodynamically stable.
    Additional Material: 1 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 28 (1990), S. 645-650 
    ISSN: 0749-1581
    Keywords: 1H NMR ; 13C NMR ; 19F NMR ; β-Diketones ; Tautomerism ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Multinuclear NMR experiments on fluorinated β-diketones have furnished information on the various tautomers present in solution and their proportions. 2-Trifluoroacetyl-1-indalone in CDCI3 solution exists in the enol form, as a mixture of exocyclic and endocyclic cis-enols with the exocyclic form favoured, but in DMF-d7 solution the equilibrium shifts to 40% enol, 60% hydrate with the enol and hydrate being in slow exchange on the NMR time scale. 2-Trifluoroacetyl-1-tetralone in CDCI3 solution exists only as the enol forms, approximately equally populated, but in DMF-d7, unlike the indalone, no hydrate is formed although there is now 6% of the keto form present in slow exchange. The experimental results were compared with calculated data produced using molecular orbital simulations. These agree with the NMR results and predict that the tetralone enol tautomers are both significantly populated at room temperature but that the indalone exists primarily as the exocyclic enol. The oxygen-oxygen internuclear distance in the hydrogen bond was estimated from the OH proton chemical shift based on a calibration from solid-state data from model compounds, and agrees well with the predictions using the molecular mechanics approach.
    Additional Material: 2 Tab.
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 31 (1993), S. 585-589 
    ISSN: 0749-1581
    Keywords: Ethanediol ; NMR ; Coupling constants ; Conformation ; Inverse detection ; Gradients ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 1H NMR spectrum of [13C]ethane-1,2-diol was measured at natural abundance using the 1H—13C inverse-detected HMQC method with magnetic field gradients. A limited solvent and temperature dependence study was undertaken and the vicinal 1H—1H coupling constants were related to those in model compounds. It is shown that the trans rotamer is significantly populated, in contradiction to some recent theoretical and experimental studies.
    Additional Material: 1 Ill.
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