Journal
BIOPHYSICAL CHEMISTRY
Volume 111, Issue 1, Pages 35-42Publisher
ELSEVIER
DOI: 10.1016/j.bpc.2004.04.002
Keywords
free radicals; hydrogen peroxide; fumarase; amyloid-like aggregation
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Hydrogen peroxide and hydroxyl-free radicals determine a diffuse aggregation of porcine fumarase and a loss of its enzymatic activity. In this study, hydroxyl-free radicals were generated in situ by irradiation with ultrasound (US) at 38 kHz. The structural characteristics of aggregated fumarase were studied using circular dichroism spectroscopy (CD) and steady state fluorescence spectroscopy. Enzyme aggregation is caused by the formation of intermolecular disufide bridges, originated by the oxidation of cysteine residues, together with a diffuse increase in U-turn in the protein's secondary structure. These conformational changes lead to a fibrous, amyloid-like aggregation which appears ordered and regular under TEM microscopy. (C) 2004 Elsevier B.V. All rights reserved.
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