Molecular Dynamics Section, National Institute on Aging, NIH, Baltimore, Maryland 21224, USA.
J Am Chem Soc. 2011 Aug 24;133(33):13010-22. doi: 10.1021/ja1115088. Epub 2011 Aug 2.
The reduction of nitrite by deoxygenated hemoglobin chains has been implicated in red cell-induced vasodilation, although the mechanism for this process has not been established. We have previously demonstrated that the reaction of nitrite with deoxyhemoglobin produces a hybrid intermediate with properties of Hb(II)NO(+) and Hb(III)NO that builds up during the reaction retaining potential NO bioactivity. To explain the unexpected stability of this intermediate, which prevents NO release from the Hb(III)NO component, we had implicated the transfer of an electron from the β-93 thiol to NO(+) producing ·SHb(II)NO. To determine if this species is formed and to characterize its properties, we have investigated the electron paramagnetic resonance (EPR) changes taking place during the nitrite reaction. The EPR effects of blocking the thiol group with N-ethyl-maleimide and using carboxypeptidase-A to stabilize the R-quaternary conformation have demonstrated that ·SHb(II)NO is formed and that it has the EPR spectrum expected for NO bound to the heme in the β-chain plus that of a thiyl radical. This new NO-related paramagnetic species is in equilibrium with the hybrid intermediate "Hb(II)NO(+) ↔ Hb(III)NO", thereby further inhibiting the release of NO from Hb(III)NO. The formation of an NO-related paramagnetic species other than the tightly bound NO in Hb(II)NO was also confirmed by a decrease in the EPR signal by -20 °C incubation, which shifts the equilibrium back to the "Hb(II)NO(+) ↔ Hb(III)NO" intermediate. This previously unrecognized NO hemoglobin species explains the stability of the intermediates and the buildup of a pool of potentially bioactive NO during nitrite reduction. It also provides a pathway for the formation of β-93 cysteine S-nitrosylated hemoglobin [SNOHb:S-nitrosohemoglobin], which has been shown to induce vasodilation, by a rapid radical-radical reaction of any free NO with the thiyl radical of this new paramagnetic intermediate.
去氧血红蛋白链还原亚硝酸盐与红细胞诱导的血管舒张有关,尽管这一过程的机制尚未确定。我们之前已经证明,亚硝酸盐与脱氧血红蛋白的反应产生一种具有 Hb(II)NO(+)和 Hb(III)NO 特性的混合中间体,在反应过程中积累,保持潜在的 NO 生物活性。为了解释这个中间体出人意料的稳定性,阻止了从 Hb(III)NO 部分释放 NO,我们推测电子从β-93 巯基转移到 NO(+),产生·SHb(II)NO。为了确定是否形成了这种物质并表征其性质,我们研究了亚硝酸盐反应过程中发生的电子顺磁共振(EPR)变化。用 N-乙基马来酰亚胺阻断巯基基团和使用羧肽酶 A 稳定 R-四元构象的 EPR 效应表明,·SHb(II)NO 已形成,并且它具有 EPR 光谱预期的 NO 结合在β链中的血红素加上硫自由基。这种新的与 NO 相关的顺磁物质与混合中间体“Hb(II)NO(+)↔Hb(III)NO”处于平衡状态,从而进一步抑制从 Hb(III)NO 释放 NO。通过在-20°C 孵育,EPR 信号降低了 20°C,从而使平衡回到“Hb(II)NO(+)↔Hb(III)NO”中间物,也证实了除了 Hb(II)NO 中紧密结合的 NO 之外,还形成了一种与 NO 相关的顺磁物质。这种以前未被认识到的 NO 血红蛋白物质解释了中间体的稳定性和亚硝酸盐还原过程中潜在生物活性的 NO 池的积累。它还提供了一种形成β-93 半胱氨酸 S-亚硝酰化血红蛋白[SNOHb:S-亚硝基血红蛋白]的途径,通过任何自由 NO 与这个新的顺磁中间体的硫自由基的快速自由基-自由基反应,已经证明它可以诱导血管舒张。