环氧化物水解酶解毒策略——可定义遗传毒性致癌物新阈值的基础。

Franz Oesch, Jan Georg Hengstler, Michael Arand
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引用次数: 14

摘要

从我们最近对环氧化物水解酶的三维结构的研究中,我们从理论上推断出两步催化机制的可能性,我们和其他人随后通过实验证实了这一机制。我们和其他人对这两步反应速率的分析表明,第一步——从体系中去除活性环氧化物——反应速度非常快(通常比第二步快三个数量级),像海绵一样吸收环氧化物。游离酶的再生(催化机制的第二步)是缓慢的。只有当环氧化物滴定出酶的剂量时,这才会成为一个毒理学问题。我们的遗传毒性工作表明,这确实产生了一个实际的阈值,低于这个阈值就没有观察到遗传毒性。这表明,与旧教条相反,对于可定义的遗传毒性致癌物存在实际阈值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Detoxication strategy of epoxide hydrolase-the basis for a novel threshold for definable genotoxic carcinogens.

From our recent work on the three-dimensional structure of epoxide hydrolases we theoretically deduced the likelihood of a two-step catalytic mechanism that we and others have subsequently experimentally confirmed. Analysis of the rate of the two steps by us and by others show that the first step-responsible for removal of the reactive epoxide from the system-works extraordinarily fast (typically three orders of magnitude faster than the second step), sucking up the epoxide like a sponge. Regeneration of the free enzyme (the second step of the catalytic mechanism) is slow. This becomes a toxicological problem only at doses of the epoxide that titrate the enzyme out. Our genotoxicity work shows that indeed this generates a practical threshold below which no genotoxicity is observed. This shows that-contrary to old dogma-practical thresholds exist for definable genotoxic carcinogens.

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