Dennis J Stuehr, Chin-Chuan Wei, Jerome Santolini, Zhi- Qiang Wang, Mika Aoyagi, Elizabeth D Getzoff
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引用次数: 19
Abstract
NOSs (nitric oxide synthases) are flavohaem enzymes that function broadly in human health and disease. We are combining mutagenesis, crystallographic and rapid kinetic methods to understand their mechanism and regulation. The NOSs create a transient tetrahydrobiopterin radical within the enzyme to generate their free radical product (NO). Recent work is revealing how critically important this process is at all levels of catalysis. This article will synthesize four seemingly disparate but related aspects of NOS tetrahydrobiopterin radical formation: (i) how it enables productive O2 activation by providing an electron to the enzyme haem, (ii) what structural features help to regulate this electron transfer, (iii) how it enables NOS to synthesize NO from its diamagnetic substrate and (iv) how it allows NOS to release NO after each catalytic cycle instead of other nitorgen oxide-containing products.
NOS(一氧化氮合酶)是一种黄酮酶,在人类健康和疾病中发挥着广泛的作用。我们正结合诱变、晶体学和快速动力学方法来了解它们的机制和调控。NOS 在酶内产生瞬时四氢生物蝶呤自由基,从而生成自由基产物(NO)。最近的研究揭示了这一过程在各级催化作用中的极端重要性。本文将综述 NOS 四氢生物蝶呤自由基形成的四个看似不同但又相关的方面:(i) 它如何通过向酶血红蛋白提供电子来实现富有成效的氧气活化;(ii) 有哪些结构特征有助于调节这种电子转移;(iii) 它如何使 NOS 从其二磁性底物中合成 NO;(iv) 它如何使 NOS 在每个催化循环后释放 NO 而不是其他含氧化萘的产物。