Proteomic modification by nitric oxide

被引:38
作者
Bian, Ka [1 ]
Ke, Yan
Kamisaki, Yoshinori
Murad, Ferid
机构
[1] Univ Texas, Sch Med, Inst Mol Med, 6431 Fannin, Houston, TX 77030 USA
[2] Univ Texas, Houston Med Sch, Dept Integrat Biol Physiol & Pharmacol, Houston, TX 77030 USA
[3] Murad Res Inst Modernized Chinese Med, Shanghai 201203, Peoples R China
[4] Shanghai Univ Trad Chinese Med, Shanghai 201203, Peoples R China
[5] Shanghai Univ E Res Inst, Nitr Oxide & Inflammatory Med, Shanghai 201203, Peoples R China
[6] Osaka Univ, Grad Sch Dent, Dept Pharmacol, Suita, Osaka 5650871, Japan
关键词
nitric oxide; inducible nitric oxide synthase (iNOS; NOS-2); nitrotyrosine; peroxidase; hemin;
D O I
10.1254/jphs.CRJ06009X
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The role of nitric oxide (NO) in cellular signaling has become one of the most rapidly growing areas in biology during the past two decades. As a gas and free radical with an unshared electron, nitric oxide participates in various biological processes. The interaction between NO and proteins may be roughly divided into two categories. In many instances, NO mediates its biological effects by activating guanylyl cyclase and elevates intracellular cyclic GMP synthesis from GTP. However, the list of cGMP-independent effects of NO is also growing at a rapid rate. In this review, the importance and relevance of nitrotyrosine formation are stressed. The utilization of intact cell cultures, tissues, and cell-free preparations along with the use of pharmacological, biochemical, and molecular biological approaches to characterize, purify, and reconstitute these NO regulatory pathways could lead to the development of new therapies for various pathological conditions that are characterized by unbalanced production of NO.
引用
收藏
页码:271 / 279
页数:9
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