Journal of Biological Chemistry · 2006 · 20 citations · 20 references
Life SciencesBiochemistryHematologyHematopathologyMetabolismRedox BiochemistryHemolytic DisordersOxidative Damage To BiomoleculesReactive Oxygen SpeciesRed Blood Cell DisordersRed Blood Cell PhysiologyRedox ChemistryHemoglobin OxidationHemolysis MechanismsHydrogen Peroxide TreatmentOxidative HemolysisRed Blood Cell Hemolysis
The effects of hydrogen peroxide on normal and acatalasemic erythrocytes were examined. Severe hemolysis of acatalasemic erythrocytes and a small tyrosine radical signal (g = 2.005) associated with the formation of ferryl hemoglobin were observed upon the addition of less than 0.25 mM hydrogen peroxide. However, when the concentration of hydrogen peroxide was increased to 0.5 mM, acatalasemic erythrocytes became insoluble in water and increased the tyrosine radical signal. Polymerization of hemoglobin and aggregation of the erythrocytes were observed. On the other hand, normal erythrocytes exhibited only mild hemolysis by the addition of hydrogen peroxide under similar conditions. From these results, the scavenging of hydrogen peroxide by hemoglobin generates the ferryl hemoglobin species (H-Hb-Fe(IV)=O) plus protein-based radicals (*Hb-Fe(IV)=O). These species induce hemolysis of erythrocytes, polymerization of hemoglobin, and aggregation of the acatalasemic erythrocytes. A mechanism for the onset of Takarara disease is proposed.
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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
Ulrich K. Laemmli · Nature · 1970 · 251.6K citations
David L. Drabkin, James H. Austin · Journal of Biological Chemistry · 1935 · 987 citations · Full text