Suppr超能文献

HRP催化HO氧化亚硝酸盐的机制再探讨:氮氧化物对酶失活及其催化活性的影响

Mechanism of HRP-catalyzed nitrite oxidation by HO revisited: Effect of nitroxides on enzyme inactivation and its catalytic activity.

作者信息

Samuni Amram, Maimon Eric, Goldstein Sara

机构信息

Institute of Medical Research Israel-Canada, Medical School, The Hebrew University of Jerusalem, Jerusalem 91120, Israel.

Nuclear Research Centre Negev, Be'er Sheva, Israel.

出版信息

Free Radic Biol Med. 2017 Jul;108:832-839. doi: 10.1016/j.freeradbiomed.2017.05.010. Epub 2017 May 8.

Abstract

The peroxidative activity of horseradish peroxidase (HRP) undergoes progressive inactivation while catalyzing the oxidation of nitrite by HO. The extent of inactivation increases as the pH increases, [nitrite] decreases or [HO] increases, and is accompanied by a loss of the Soret peak of HRP along with yellow-greenish coloration of the solution. HRP-catalyzed nitrite oxidation by HO involves not only the formation of compounds I and II as transient heme species, but also compound III, all of which in turn, oxidize nitrite yielding NO. The rate constant of nitrite oxidation by compound III is at least 10-fold higher than that by compound II, which is also reducible by NO where its reduction by nitrite is the rate-determining step of the catalytic cycle. The extent of the loss of the Soret peak of HRP is lower than the loss of its peroxidative activity implying that deterioration of the heme moiety leading to iron release only partially contributes toward heme inactivation. Cyclic stable nitroxide radicals, such as 2,2,6,6-tetramethyl-piperidine-N-oxyl (TPO), 4-OH-TPO and 4-NH-TPO at µM concentrations detoxify NO thus protecting HRP against inactivation mediated by this radical. Hence, HRP inactivation proceeds via nitration of the porphyrin ring most probably through compound I reaction with NO, which partially leads to deterioration of the heme moiety. The nitroxide acts catalytically since its oxidation by NO yields the respective oxoammonium cation, which is readily reduced back to the nitroxide by HO, superoxide ion radical, and nitrite. In addition, the nitroxide catalytically inhibits tyrosine nitration mediated by HRP/HO/nitrite reactions system as it efficiently competes with tyrosyl radical for NO. The inhibition by nitroxides of tyrosine nitration is demonstrated also in the case of microperoxidase (MP-11) and cytochrome c revealing an additional role played by nitroxide antioxidants.

摘要

辣根过氧化物酶(HRP)的过氧化活性在催化HO氧化亚硝酸盐的过程中会逐渐失活。失活程度随pH值升高、[亚硝酸盐]降低或[HO]升高而增加,同时伴随着HRP的Soret峰消失以及溶液呈现黄绿色。HRP催化HO氧化亚硝酸盐不仅涉及形成作为瞬时血红素物种的化合物I和II,还涉及化合物III,所有这些化合物依次氧化亚硝酸盐生成NO。化合物III氧化亚硝酸盐的速率常数至少比化合物II高10倍,化合物II也可被NO还原,其中亚硝酸盐对其还原是催化循环的速率决定步骤。HRP的Soret峰损失程度低于其过氧化活性损失,这意味着导致铁释放的血红素部分降解仅部分导致血红素失活。微摩尔浓度的环状稳定氮氧自由基,如2,2,6,6 - 四甲基哌啶 - N - 氧基(TPO)、4 - OH - TPO和4 - NH - TPO可使NO解毒,从而保护HRP免受该自由基介导的失活。因此,HRP失活最可能是通过卟啉环的硝化作用,这可能是通过化合物I与NO反应实现的,这部分导致了血红素部分的降解。氮氧自由基起催化作用,因为它被NO氧化生成相应的氧鎓铵阳离子,该阳离子很容易被HO、超氧离子自由基和亚硝酸盐还原回氮氧自由基。此外,氮氧自由基催化抑制由HRP/HO/亚硝酸盐反应系统介导的酪氨酸硝化,因为它能有效地与酪氨酸自由基竞争NO。在微过氧化物酶(MP - 11)和细胞色素c的情况下也证明了氮氧自由基对酪氨酸硝化的抑制作用,这揭示了氮氧自由基抗氧化剂的额外作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验