Kang J H, Kim S M
Department of Genetic Engineering, Chongju University, Korea.
Mol Cells. 1997 Dec 31;7(6):777-82.
To study the catalytic activity of Cu,Zn-superoxide dismutase (SOD) in the generation of hydroxyl radical (.OH) from H2O2, we investigated the mechanism of DNA cleavage mediated by human Cu,Zn-SOD and H2O2. When plasmid DNA was incubated with 5 microM Cu, Zn-SOD and 1.0 mM H2O2, DNA cleavage occurred within 15 min. A spectrophotometric study using a 2,2'-azinobis-(3-ethylbenzthiazoline-6-sulfonate) (ABTS) showed that free .OH formation was proportional to concentrations of Cu,Zn-SOD and H2O2. .OH formation and DNA cleavage were inhibited by hydroxyl radical scavengers such as cyanide, azide, and formate. These results indicated that .OH generated early in the peroxidative reaction of Cu,Zn-SOD with H2O2 was implicated in DNA cleavage. Incubation with H2O2 resulted in a time-dependent release of copper ions from the Cu,Zn-SOD molecule. The released copper ions then likely participated in a Fenton-like reaction to produce .OH that may have caused DNA cleavage. Evidence that DTPA protected the DNA cleavage induced by the Cu,Zn-SOD/H2O2 system supports this mechanism. We suggest that DNA cleavage is mediated in the Cu,Zn-SOD/H2O2 system via the generation of .OH by a combination of the peroxidative reaction of Cu,Zn-SOD and the Fenton-like reaction of free copper ions released from oxidatively damaged SOD.
为了研究铜锌超氧化物歧化酶(SOD)在由过氧化氢(H₂O₂)生成羟基自由基(·OH)过程中的催化活性,我们研究了人铜锌超氧化物歧化酶和H₂O₂介导的DNA切割机制。当质粒DNA与5微摩尔/升的铜锌超氧化物歧化酶和1.0毫摩尔/升的H₂O₂一起孵育时,15分钟内就发生了DNA切割。使用2,2'-联氮双(3-乙基苯并噻唑啉-6-磺酸)(ABTS)进行的分光光度研究表明,游离·OH的形成与铜锌超氧化物歧化酶和H₂O₂的浓度成正比。·OH的形成和DNA切割受到羟基自由基清除剂如氰化物、叠氮化物和甲酸盐的抑制。这些结果表明,铜锌超氧化物歧化酶与H₂O₂的过氧化反应早期产生的·OH与DNA切割有关。与H₂O₂孵育导致铜离子从铜锌超氧化物歧化酶分子中随时间释放。释放出的铜离子随后可能参与类Fenton反应以产生可能导致DNA切割的·OH。二乙三胺五乙酸(DTPA)保护铜锌超氧化物歧化酶/H₂O₂系统诱导的DNA切割这一证据支持了该机制。我们认为,在铜锌超氧化物歧化酶/H₂O₂系统中,DNA切割是通过铜锌超氧化物歧化酶的过氧化反应与氧化损伤的超氧化物歧化酶释放的游离铜离子的类Fenton反应相结合产生·OH来介导的。