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Copper-Catalyzed Tyrosine Nitration

机译:铜催化酪氨酸硝化

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摘要

Tyrosine nitration, often observed during neurodegenerative disorders under nitrative stress, is usually considered to be induced chemically either by nitric oxide and oxygen forming nitrogen dioxide or by the decomposition of peroxynitrite. It can also be induced enzymatically byperoxidases or superoxide dismutases in the presence of both hydrogen peroxide and nitrite forming nitrogen dioxide and/or peroxynitrite. In this study, the role of cupric ions for catalyzing tyrosine nitration in the presence of hydrogen peroxide and nitrite, by a chemical mechanism rather similar to enzymatic pathways where nitrite is oxidized to form nitrogen dioxide, was investigated by development of a microreactor also capable of acting as an emitter for electrospray ionization mass spectrometry analysis. Indeed, cupric ions and peptide-cupric ion complexes are found to be excellent Fenton catalysts, even better than Fe(III) or heme, for the formation of *OH radicals and/or copper(II)-bound *OH radicals from hydrogen peroxide. These radicals are efficiently scavenged by nitrite anions to form *NO_2 and by tyrosine to form tyrosine radicals, leading to tyrosine nitration in polypeptides. We also show that cupric ions can catalyze tyrosine nitration from nitric oxide, oxygen, and hydrogen peroxide as the formation of tyrosine radicals is increased in the presence of diffusible and/or copper(II) bound hydroxyl radicals. This study shows that copper has a polyvalent role in the processes of tyrosine nitration.
机译:酪氨酸硝化通常在硝化应激下神经退行性疾病期间观察到,通常被认为是由一氧化氮和氧形成二氧化氮或过氧亚硝酸盐的分解化学诱导的。在过氧化氢和亚硝酸盐形成二氧化氮和/或过亚硝酸盐的情况下,过氧化物酶或超氧化物歧化酶也可通过酶促诱导它。在这项研究中,研究了铜离子在过氧化氢和亚硝酸盐存在下催化酪氨酸硝化的作用,其化学机理与酶促途径(其中亚硝酸盐被氧化形成二氧化氮的途径)相似,是通过开发一种微反应器来研究的。用作电喷雾电离质谱分析的发射器。实际上,发现铜离子和肽-铜离子络合物是出色的Fenton催化剂,甚至比Fe(III)或血红素更好,它们可以由过氧化氢形成* OH自由基和/或与铜(II)结合的* OH自由基。 。这些自由基被亚硝酸根阴离子有效清除形成* NO_2,并被酪氨酸清除形成酪氨酸自由基,从而导致多肽中的酪氨酸硝化。我们还表明,铜铜离子可以催化一氧化氮,氧气和过氧化氢中的酪氨酸硝化,因为在存在可扩散和/或铜(II)结合的羟基自由基时,酪氨酸自由基的形成增加了。这项研究表明,铜在酪氨酸硝化过程中具有多价作用。

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  • 来源
    《Journal of the American Chemical Society》 |2011年第49期|p.19823-19831|共9页
  • 作者单位

    Laboratoire d'Electrochimie Physique et Analytique, Ecole Polytechnique Federate de Lausanne, Station 6, CH-1015 Lausanne, Switzerland;

    Laboratoire d'Electrochimie Physique et Analytique, Ecole Polytechnique Federate de Lausanne, Station 6, CH-1015 Lausanne, Switzerland;

    Department of Chemistry, Institute of Biomedical Sciences, Fudan University, Shanghai 200433, People's Republic of China;

    Laboratoire d'Electrochimie Physique et Analytique, Ecole Polytechnique Federate de Lausanne, Station 6, CH-1015 Lausanne, Switzerland;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-18 03:14:35

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