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  • 1
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ultraviolet absorption and static fluorescence properties of hexanucleotide (Gm-A-A-Y-A-ψp) and a dodecanucleotide (A-Cm-U-Gm-A-A-Y-A-ψ-m5C-U-Gp) excised from the anticodon region of phenylalanine tRNA from yeast have been studied with respect to temperature, pH, ionic strength, and Mg2+ concentration. At low temperature these oligomers have a largely stacked structure. Only the melting data of the dodecanucleotide in absence of Mg2+ fit a two-state model. From the different melting behavior of the oligonucleotides after excision of base Y, a rodlike structure of the hexanucleotide produced by stacking interactions can be concluded. The Y fluorescence increase produced by Mg2+ has been used to evaluate the binding equilibria between Mg2+ and the oligonucleotides. One strong binding site per oligonucleotide and a greater number of weak binding sites have been found. The fluorescence of the free base Y is not influenced by Mg2+. The dodecanucleotide enhances the ethidium fluorescence to the same extent as tRNAPhe and produces comparable shifts in the excitation and emission spectra. Therefore a double helical structure for this oligomer under the assay conditions is suggested. Only weak binding of ethidium to the hexanucleotide is observed, indicating that intercalation of the dye into its structure is not favored. The data show the decisive role of the nucleobase Y in maintaining a rigid stacked structure of the anticodon nucleotides. This structure is stabilized by high ionic strength, Mg2+, and ethidium.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Das „maßgeschneiderte“ Arzneimittel ist ein alter Traum seit Paracelsus′: „Dosis sola facit venenum“. Ein ideales Pharmakon sollte den pathologischen Vorgang oder den parasitären Organismus maximal inhibieren und dabei den menschlichen Körper minimal schädigen. Um dieses Ziel zu erreichen, muß man versuchen, metabolische Unterschiede zwischen dem pathologischen bzw. parasitären und dem normalen menschlichen Stoffwechsel gezielt auszunutzen. Dies erscheint heute aufgrund der vertieften Kenntnisse enzymatischer Vorgänge ein möglicher, sogar vielversprechender Weg. Das Pharmakon sollte dabei an einem zentral wichtigen Prozeß eingreifen. Ein solcher Prozeß ist die Proteinbiosynthese, bei der die erforderliche Genauigkeit im Zusammenbau der Makromoleküle durch den Vorgang des „Korrekturlesens“ erreicht wird. Es zeigt sich, daß dieser Mechanismus je nach Spezies verschieden verläuft.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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