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  • Articles: DFG German National Licenses  (2)
  • Fluorescence lifetime  (1)
  • Rekker's hydrophobic fragmental constant  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    European biophysics journal 11 (1985), S. 243-248 
    ISSN: 1432-1017
    Keywords: Fluorescence lifetime ; tryptophan residues ; neurotoxins
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Physics
    Notes: Abstract The fluorescence lifetime and rotational correlation time of the single tryptophan residue in α-cobratoxin have been measured between pH 2 and 10. The fluorescence decays are non-exponential and give lifetimes that are shorter than normally observed in small proteins (0.3 ns and 1 ns). This emission is consistent with a model in which the tryptophan residue is in slightly different environments in the protein. Fluorescence anisotropy decays show that the tryptophan residue is almost completely immobilised by neighbouring groups in the protein. The range of the “wobbling” motion is slightly pH dependent and limited to between 5° and 10°.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 4 (1981), S. 454-460 
    ISSN: 0935-6304
    Keywords: Reversed-phase mode liquid chromatography ; Rekker's hydrophobic fragmental constant ; Calculation of concentration of organic modifier ; Prediction of retention time ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The utility of Rekker's hydrophobic fragmental constant has been examined for optimization of reversed-phase mode liquid chromatographic separations. The chromatographic behavior of about 60 non-ionic compounds was measured in different acetonitrile/water mixtures and the logarithm of their capacity factors (log k) was correlated with their calculated hydrophobicities (log P). Linear relations were found in each case between log k and log P. The slope of the various lines was related to the percentage concentration of acetonitrile in the mobile phase. It was shown that, by using nine stand ard compounds and measuring their capacity factors in five eluents with different acetonitrile concentrations, the retention time could be predicted for 60 compounds. Calculation of the concentration of the organic modifier was also possible in a system of well coated octadecyl bonded packings with acetonitrile/water mixtures as eluent. Prediction of the capacity factor was accomplished to within 5% error.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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