Miller R T, Martásek P, Roman L J, Nishimura J S, Masters B S
Department of Biochemistry, The University of Texas Health Science Center at San Antonio, San Antonio, Texas 78284-7760, USA.
Biochemistry. 1997 Dec 9;36(49):15277-84. doi: 10.1021/bi972022c.
Neuronal nitric oxide synthase (nNOS) is a modular enzyme which consists of a flavin-containing reductase domain and a heme-containing oxygenase domain, linked by a stretch of amino acids which contains a calmodulin (CaM) binding site. CaM binding to nNOS facilitates the transfer of NADPH-derived electrons from the reductase domain to the oxygenase domain, resulting in the conversion of L-arginine to L-citrulline with the concomitant formation of a guanylate cyclase activating factor, putatively nitric oxide. Numerous studies have established that peroxynitrite-derived nitrogen oxides are present following nNOS turnover. Since peroxynitrite is formed by the diffusion-limited reaction between the two radical species, nitric oxide and O2.-, we employed the adrenochrome assay to examine whether nNOS was capable of producing O2.- during catalytic turnover in the presence of L-arginine. To differentiate between the role played by the reductase domain and that of the oxygenase domain in O2.- production, we compared its production by nNOS against that of a nNOS mutant (CYS-331), which was unable to transfer NADPH-derived electrons efficiently to the heme iron under special conditions, and against that of a flavoprotein module construct of nNOS. We report that O2.- production by nNOS and the CYS-331 mutant is CaM-dependent and that O2.- production can be modulated by substrates and inhibitors of nNOS. O2.- was also produced by the reductase domain of nNOS; however, it did not display the same CaM dependency. We conclude that both the reductase and oxygenase domains of nNOS produce O2.-, but that the reductase domain is both necessary and sufficient for O2.- production.
神经元型一氧化氮合酶(nNOS)是一种模块化酶,由一个含黄素的还原酶结构域和一个含血红素的加氧酶结构域组成,二者通过一段含有钙调蛋白(CaM)结合位点的氨基酸相连。CaM与nNOS结合促进了来自还原酶结构域的NADPH衍生电子向加氧酶结构域的转移,导致L - 精氨酸转化为L - 瓜氨酸,并伴随形成一种鸟苷酸环化酶激活因子,推测为一氧化氮。大量研究表明,nNOS周转后会产生过氧亚硝酸盐衍生的氮氧化物。由于过氧亚硝酸盐是由两种自由基一氧化氮和超氧阴离子(O2.-)之间的扩散限制反应形成的,我们采用肾上腺色素测定法来检测nNOS在L - 精氨酸存在下催化周转过程中是否能够产生O2.-。为了区分还原酶结构域和加氧酶结构域在O2.-产生中所起的作用,我们将nNOS产生O2.-的情况与一种nNOS突变体(CYS - 331)进行了比较,该突变体在特殊条件下无法有效地将NADPH衍生的电子转移至血红素铁,同时还与nNOS的黄素蛋白模块构建体进行了比较。我们报告称,nNOS和CYS - 331突变体产生O2.-是依赖CaM的,并且O2.-的产生可被nNOS的底物和抑制剂调节。nNOS的还原酶结构域也能产生O2.-;然而,它并不表现出相同的CaM依赖性。我们得出结论,nNOS的还原酶结构域和加氧酶结构域都能产生O2.-,但还原酶结构域对于O2.-的产生既是必要的也是充分的。