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Functional site profiling and electrostatic analysis of cysteines modifiable to cysteine sulfenic acid.可修饰为半胱氨酸亚磺酸的半胱氨酸的功能位点分析及静电分析
Protein Sci. 2008 Feb;17(2):299-312. doi: 10.1110/ps.073096508.
2
Structure of the sulphiredoxin-peroxiredoxin complex reveals an essential repair embrace.硫氧还蛋白-过氧化物酶复合体的结构揭示了一种关键的修复环抱机制。
Nature. 2008 Jan 3;451(7174):98-101. doi: 10.1038/nature06415.
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Substrate specificity and redox potential of AhpC, a bacterial peroxiredoxin.细菌过氧化物还原酶AhpC的底物特异性和氧化还原电位
Proc Natl Acad Sci U S A. 2008 Jun 17;105(24):8209-14. doi: 10.1073/pnas.0708308105. Epub 2007 Dec 28.
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The catalytic mechanism of peroxiredoxins.过氧化物氧化还原酶的催化机制。
Subcell Biochem. 2007;44:61-81. doi: 10.1007/978-1-4020-6051-9_4.
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Structural survey of the peroxiredoxins.过氧化物酶的结构研究
Subcell Biochem. 2007;44:41-60. doi: 10.1007/978-1-4020-6051-9_3.
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Reactivity of sulfenic acid in human serum albumin.人血清白蛋白中次磺酸的反应活性。
Biochemistry. 2008 Jan 8;47(1):358-67. doi: 10.1021/bi701520y. Epub 2007 Dec 14.
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Fluorescent and affinity-based tools to detect cysteine sulfenic acid formation in proteins.用于检测蛋白质中半胱氨酸亚磺酸形成的基于荧光和亲和力的工具。
Bioconjug Chem. 2007 Nov-Dec;18(6):2004-17. doi: 10.1021/bc700257a. Epub 2007 Nov 21.
8
A genetically encoded probe for cysteine sulfenic acid protein modification in vivo.一种用于体内半胱氨酸亚磺酸蛋白质修饰的基因编码探针。
Biochemistry. 2007 Dec 18;46(50):14725-32. doi: 10.1021/bi701625s. Epub 2007 Nov 20.
9
S-nitrosylation of peroxiredoxin 2 promotes oxidative stress-induced neuronal cell death in Parkinson's disease.过氧化物氧化还原酶2的S-亚硝基化促进帕金森病中氧化应激诱导的神经元细胞死亡。
Proc Natl Acad Sci U S A. 2007 Nov 20;104(47):18742-7. doi: 10.1073/pnas.0705904104. Epub 2007 Nov 14.
10
The requirement of reversible cysteine sulfenic acid formation for T cell activation and function.T细胞活化和功能对可逆性半胱氨酸亚磺酸形成的需求。
J Immunol. 2007 Nov 15;179(10):6456-67. doi: 10.4049/jimmunol.179.10.6456.

发现信号介导的半胱氨酸氧化机制。

Discovering mechanisms of signaling-mediated cysteine oxidation.

作者信息

Poole Leslie B, Nelson Kimberly J

机构信息

Department of Biochemistry, Center for Structural Biology, Wake Forest University School of Medicine, Winston-Salem, NC 27157, United States.

出版信息

Curr Opin Chem Biol. 2008 Feb;12(1):18-24. doi: 10.1016/j.cbpa.2008.01.021. Epub 2008 Mar 7.

DOI:10.1016/j.cbpa.2008.01.021
PMID:18282483
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2408887/
Abstract

Accumulating evidence reveals hydrogen peroxide as a key player both as a damaging agent and, from emerging evidence over the past decade, as a second messenger in intracellular signaling. This rather mild oxidant acts upon downstream targets within signaling cascades to modulate the activity of a host of enzymes (e.g. phosphatases and kinases) and transcriptional regulators through chemoselective oxidation of cysteine residues. With the recent development of specific detection reagents for hydrogen peroxide and new chemical tools to detect the generation of the initial oxidation product, sulfenic acid, on reactive cysteines within target proteins, the scene is set to gain a better understanding of the mechanisms through which hydrogen peroxide acts as a second messenger in cell signaling.

摘要

越来越多的证据表明,过氧化氢既是一种破坏剂,也是一种细胞内信号传导的第二信使(基于过去十年新出现的证据)。这种相对温和的氧化剂作用于信号级联反应中的下游靶点,通过对半胱氨酸残基进行化学选择性氧化来调节许多酶(如磷酸酶和激酶)和转录调节因子的活性。随着过氧化氢特异性检测试剂以及用于检测目标蛋白中反应性半胱氨酸上初始氧化产物亚磺酸生成的新化学工具的最新发展,我们有望更好地理解过氧化氢在细胞信号传导中作为第二信使的作用机制。