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使用铼(咪唑 - 烷基 - 硝基精氨酸)敏化剂 - 导线探究诱导型一氧化氮合酶的血红素配位状态。

Probing heme coordination states of inducible nitric oxide synthase with a ReI(imidazole-alkyl-nitroarginine) sensitizer-wire.

作者信息

Le Nguyen Yen Hoang, Winkler Jay R, Gray Harry B

机构信息

Beckman Institute, California Institute of Technology, Pasadena, California 91125, USA.

出版信息

J Phys Chem B. 2007 Jun 21;111(24):6628-33. doi: 10.1021/jp071405+. Epub 2007 May 31.

Abstract

Mammalian inducible nitric oxide synthase (iNOS) catalyzes the production of l-citrulline and nitric oxide (NO) from L-arginine and O2. The Soret peak in the spectrum of the iNOS heme domain (iNOSoxy) shifts from 423 to 390 nm upon addition of a sensitizer-wire, [ReI-imidazole-(CH2)8-nitroarginine]+, or [ReC8argNO2]+, owing to partial displacement of the water ligand in the active site. From analysis of competitive binding experiments with imidazole, the dissociation constant (Kd) for [ReC8argNO2]+-iNOSoxy was determined to be 3.0+/-0.1 microM, confirming that the sensitizer-wire binds with higher affinity than both L-arginine (Kd=22+/-5 microM) and imidazole (Kd=14+/-3 microM). Laser excitation (355 nm) of [ReC8argNO2]+-iNOSoxy triggers electron transfer to the active site of the enzyme, producing a ferroheme in less than approximately 1 micros.

摘要

哺乳动物诱导型一氧化氮合酶(iNOS)催化由L-精氨酸和O2生成L-瓜氨酸和一氧化氮(NO)。在添加敏化剂导线[ReI-咪唑-(CH2)8-硝基精氨酸]+或[ReC8argNO2]+后,iNOS血红素结构域(iNOSoxy)光谱中的索雷特峰从423 nm移至390 nm,这是由于活性位点中的水配体部分被取代。通过对咪唑竞争性结合实验的分析,确定[ReC8argNO2]+-iNOSoxy的解离常数(Kd)为3.0±0.1 μM,证实敏化剂导线的结合亲和力高于L-精氨酸(Kd = 22±5 μM)和咪唑(Kd = 14±3 μM)。[ReC8argNO2]+-iNOSoxy的激光激发(355 nm)触发电子转移至酶的活性位点,在不到约1微秒的时间内产生亚铁血红素。

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