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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biospectroscopy 3 (1997), S. 435-444 
    ISSN: 1075-4261
    Keywords: transferrin ; Raman ; absorption ; mutants ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Physics
    Notes: The resonance Raman (RR) data for a variety of transferrin samples were investigated to explore differences between the two active sites. The excitation wavelength dependence of the RR data in the low energy shift region (〈900 cm-1) for diferric transferrin (Fe2Tf) reveals extensive changes in the relative intensities for some of the peaks, indicating that the visible and near ultraviolet absorption of the Fe2Tf protein is composed of several distinct transitions. The identity of the low-energy vibrations was explored by comparison of the data from Fe2Tf, two different binding site mutants of the N-terminal site half transferrin molecule, Tf/2N, and Fe2Tf in which the normal binding site carbonate was replaced with C18O32-. The higher energy RR spectra of the various samples are quite similar, whereas the low-energy band patterns are strongly influenced by the mutations and isotopic substitution. Comparison of the RR data obtained from Fe2Tf, Tf/2N, and C-terminal monoferric transferrin reveals that the intensities and energies of the modes below 900 cm-1 are different for the two binding sites. This result helps reveal an isolated electronic transition for the N-terminal active site near 365 nm, where laser excitation yields selective enhancement of the low-energy N-terminal modes. © 1997 John Wiley & Sons, Inc. Biospectroscopy 3: 435-444, 1997
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1075-4261
    Keywords: pterins ; FTIR ; vibrational analysis ; solvent effects ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Physics
    Notes: Fourier transform infrared (FTIR) spectra have been obtained from solution samples of the heterocycles uracil, lumazine, and violapterin and reveal interpretable carbonyl stretching frequencies. Spectra of conjugate bases of lumazine and violapterin demonstrate decreases in these carbonyl stretching frequencies upon ionization. Based on isotopic shifts from amide deuterated analogs, semiempirical QCFF/PI calculations were used to assign the vibrational frequencies in the region 1100-1800 cm-1 observed from samples in dimethylsulfoxide (DMSO) and aqueous solutions to specific normal modes. The observed deuterium shifts and the calculations suggest that, in some cases, N - H bending motions are coupled to the C=O stretching motions of the pyrimidine ring. These data suggest that for lumazine anions a change in solvent can significantly change the mixing of the N - H bending and C=O stretching vibrational motions. This implies that vibrational analysis for lumazine species in relatively noninteracting media like nonpolar solvents, mulls or pellets cannot necessarily be transferred to the system when it is dissolved in a polar, hydrogen-bonding solvent such as water. Although other explanations can be offered, our vibrational analysis suggests that the changes in normal mode composition of the predominantly C=O stretching vibrations of lumazine anion on going from dimethylsulfoxide to water solution are consistent with a change in the predominant tautomer of the heterocycle. This change appears to correspond to a shifting of the location of the remaining acidic proton to a different ring nitrogen atom. This interpretation is of interest in view of recent ab initio calculations which suggest that proton shifts may occur during the hydroxylation of lumazine as mediated by the enzyme xanthine oxidase. © 1998 John Wiley & Sons, Inc. Biospectroscopy 4: 235-256, 1998
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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