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Biomedical subjects

G Tourillon

Publications and source records attributed to G Tourillon.

18 recordsLinked to original sources
PubMed1992

X-ray absorption spectroscopy of carbonyl basket handle Fe(II) porphyrins: the distortion of the tetrapyrrolic macrocycle.

The distortion of the tetrapyrrolic macrocycle, the Fe-C-O bond angle and the Fe local electronic structure of carbonyl basket-handle Fe2+ porphyrins as a function of the basket-handle chain length have been studied by X-ray absorption near edge structure (XANES) spectroscopy, both in the solid state and in toluene solution. The Fe-C-O bond angle has been found to be linear in all compounds while the increasing distortion of the macrocycle with shortening of the chain length is indicated by the multiple scattering resonance in the heme plane appearing at 22 eV in the XANES spectrum.

Iron↗
PubMed1990

Rapid reduction of iron in horse spleen ferritin by thioglycolic acid measured by dispersive X-ray absorption spectroscopy.

The release of iron from ferritin is important in the formation of iron proteins and for the management of diseases in both animals and plants associated with abnormal accumulations of ferritin iron. Much more iron can be released experimentally by reduction of the ferric hydrous oxide core than by chelation of Fe3+ which has led to the notion that reduction is also the major aspect of iron release in vivo. Variations in the kinetics of reduction of the mineral core of ferritin have been attributed to the redox potential of the reductant, redox properties of the iron core, the structure of the protein coat, the analytical method used to detect Fe2+ and reactions at the surface of the mineral. Direct measurements of the oxidation state of the iron during reduction has never been used to analyze the kinetics of reduction, although Mössbauer spectroscopy has been used to confirm the extent of reduction after electrochemical reduction using dispersive X-ray absorption spectroscopy (DXAS). We show that the near edge of X-ray absorption spectra (XANES) can be used to quantify the relative amounts of Fe2+ and Fe3+ in mixtures of the hydrated ions. Since the nearest neighbors of iron in the ferritin iron core do not change during reduction, XANES can be used to monitor directly the reduction of the ferritin iron core. Previous studies of iron core reduction which measured by Fe2+.bipyridyl formation, or coulometric reduction with different mediators, suggested that rates depended mainly on the redox potential of the electron donor.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗