一氧化氮合酶超氧化物的EPR自旋捕获

J. Vasquez-Vivar, J. Joseph, H. Karoui, Hao Zhang, J. Miller, P. Martásek
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引用次数: 8

摘要

15n)- EMPO显著提高了电子对磁共振(EPR)超氧化物检测的灵敏度。不像5,5-二甲基-1-吡啶n -氧化物(DMPO),一种常用的超氧化物自旋陷阱,DEPMPO和EMPO形成的超氧化物加合物是持久的,它不会衰变为相应的羟基加合物。使用这些新的自旋阱,超氧化物的epr检测现在是直接和更敏感的。这些新的超氧化物陷阱与环隙谐振器技术相结合,使我们能够明确地证明一氧化氮合酶的内皮和神经元异构体形成超氧化物。超氧化物通过钙/钙调素依赖机制在酶的氧合酶区域形成。讨论了四氢生物蝶呤辅助因子和NOS抑制剂对超氧化物释放的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
EPR spin trapping of superoxide from nitric oxide synthase
15 N)- EMPO has significantly improved the sen- sitivity of superoxide detection by electron para- magnetic resonance (EPR). Unlike 5,5-dimethyl-1- pyrroline N-oxide (DMPO), a commonly used superoxide spin trap, both DEPMPO and EMPO form superoxide adducts that are persistent, which do not decay to the corresponding hydroxyl adduct. Using these new spin traps, the EPR-detection of superoxide is now straightfor- ward and more sensitive. These new superoxide traps in combination with the loop gap resonator technology have enabled us to demonstrate unequivocally the formation of superoxide from the endothelial and neuronal isoforms of nitric oxide synthase. Superoxide is formed at the oxy- genase domain of the enzyme by a calcium/ calmodulin dependent mechanism. The effect of tetrahydrobiopterin cofactor and NOS inhibitors on the release of superoxide is discussed.
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