Bakker G R, Boyer R F
J Biol Chem. 1986 Oct 5;261(28):13182-5.
Apoferritin catalyzes the oxidation of Fe(II) to Fe(III). Ferroxidase activity is assayed and characterized by coupling the oxidation with the binding of Fe(III) to transferrin. The initial rate of Fe(II) oxidation is dependent on apoferritin and initial Fe(II) concentration but independent of transferrin concentration. The ferroxidase activity is inhibited by Zn(II). Ferritins with varying loads of iron have the same ferroxidase activity level. It is suggested that the described oxidation process represents the initial step of iron deposition in apoferritin. Since transferrin can intercept Fe(III) before it is deposited in apoferritin, active sites for Fe(II) oxidation must be on or near the surface of apoferritin. This finding is contrary to the current view of apoferritin-catalyzed oxidation of Fe(II) which places active sites in the channels to the core or inside the central core.
脱铁铁蛋白催化Fe(II)氧化为Fe(III)。通过将Fe(III)与转铁蛋白的结合与氧化反应偶联来测定和表征铁氧化酶活性。Fe(II)氧化的初始速率取决于脱铁铁蛋白和初始Fe(II)浓度,但与转铁蛋白浓度无关。铁氧化酶活性受到Zn(II)的抑制。具有不同铁负载量的铁蛋白具有相同的铁氧化酶活性水平。有人认为,所描述的氧化过程代表了铁在脱铁铁蛋白中沉积的初始步骤。由于转铁蛋白可以在Fe(III)沉积到脱铁铁蛋白之前将其截获,因此Fe(II)氧化的活性位点必须在脱铁铁蛋白的表面上或附近。这一发现与目前关于脱铁铁蛋白催化Fe(II)氧化的观点相反,后者将活性位点置于通向核心的通道中或中央核心内部。