Hannibal Luciana, Page Richard C, Haque Mohammad Mahfuzul, Bolisetty Karthik, Yu Zhihao, Misra Saurav, Stuehr Dennis J
*Department of Pathobiology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, U.S.A.
‡Department of Molecular Cardiology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, U.S.A.
Biochem J. 2015 Apr 1;467(1):153-65. doi: 10.1042/BJ20141319.
Nitric oxide synthases (NOSs) are haem-thiolate enzymes that catalyse the conversion of L-arginine (L-Arg) into NO and citrulline. Inducible NOS (iNOS) is responsible for delivery of NO in response to stressors during inflammation. The catalytic performance of iNOS is proposed to rely mainly on the haem midpoint potential and the ability of the substrate L-Arg to provide a hydrogen bond for oxygen activation (O-O scission). We present a study of native iNOS compared with iNOS-mesohaem, and investigate the formation of a low-spin ferric haem-aquo or -hydroxo species (P) in iNOS mutant W188H substituted with mesohaem. iNOS-mesohaem and W188H-mesohaem were stable and dimeric, and presented substrate-binding affinities comparable to those of their native counterparts. Single turnover reactions catalysed by iNOSoxy with L-Arg (first reaction step) or N-hydroxy-L-arginine (second reaction step) showed that mesohaem substitution triggered higher rates of Fe(II)O₂ conversion and altered other key kinetic parameters. We elucidated the first crystal structure of a NOS substituted with mesohaem and found essentially identical features compared with the structure of iNOS carrying native haem. This facilitated the dissection of structural and electronic effects. Mesohaem substitution substantially reduced the build-up of species P in W188H iNOS during catalysis, thus increasing its proficiency towards NO synthesis. The marked structural similarities of iNOSoxy containing native haem or mesohaem indicate that the kinetic behaviour observed in mesohaem-substituted iNOS is most heavily influenced by electronic effects rather than structural alterations.
一氧化氮合酶(NOSs)是血红素硫醇盐酶,可催化L-精氨酸(L-Arg)转化为NO和瓜氨酸。诱导型NOS(iNOS)负责在炎症期间应对应激源时释放NO。iNOS的催化性能主要依赖于血红素中点电位以及底物L-Arg为氧活化(O-O断裂)提供氢键的能力。我们对天然iNOS与中血红素iNOS进行了比较研究,并研究了用中血红素替代的iNOS突变体W188H中低自旋铁血红素-水合或-羟基物种(P)的形成。中血红素iNOS和W188H-中血红素是稳定的二聚体,其底物结合亲和力与其天然对应物相当。由iNOSoxy催化的L-Arg(第一步反应)或N-羟基-L-精氨酸(第二步反应)的单周转反应表明,中血红素替代引发了更高的Fe(II)O₂转化率,并改变了其他关键动力学参数。我们阐明了用中血红素替代的NOS的第一个晶体结构,发现与携带天然血红素的iNOS结构基本相同。这有助于剖析结构和电子效应。中血红素替代在催化过程中大大减少了W188H iNOS中物种P的积累,从而提高了其合成NO的效率。含有天然血红素或中血红素的iNOSoxy的显著结构相似性表明,在中血红素替代的iNOS中观察到的动力学行为受电子效应而非结构改变的影响最大。