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本文引用的文献

1
Redox proteomics: from protein modifications to cellular dysfunction and disease.氧化还原蛋白质组学:从蛋白质修饰到细胞功能障碍与疾病
Mass Spectrom Rev. 2014 Jan-Feb;33(1):1-6. doi: 10.1002/mas.21404.
2
Redox proteomics in selected neurodegenerative disorders: from its infancy to future applications.氧化还原蛋白质组学在一些神经退行性疾病中的应用:从起步到未来展望。
Antioxid Redox Signal. 2012 Dec 1;17(11):1610-55. doi: 10.1089/ars.2011.4109. Epub 2012 Jan 18.
3
Identification of the oxidative stress proteome in the brain.脑内氧化应激蛋白质组的鉴定。
Free Radic Biol Med. 2011 Feb 15;50(4):487-94. doi: 10.1016/j.freeradbiomed.2010.11.021. Epub 2010 Nov 25.
4
Oxidative stress and human diseases: Origin, link, measurement, mechanisms, and biomarkers.氧化应激与人类疾病:起源、关联、检测、机制与生物标志物。
Crit Rev Clin Lab Sci. 2009;46(5-6):241-81. doi: 10.3109/10408360903142326.
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Protein S-glutathionylation: a regulatory device from bacteria to humans.蛋白质S-谷胱甘肽化:从细菌到人类的一种调控机制
Trends Biochem Sci. 2009 Feb;34(2):85-96. doi: 10.1016/j.tibs.2008.11.002. Epub 2009 Jan 8.
6
Redox proteomics identification of oxidatively modified brain proteins in Alzheimer's disease and mild cognitive impairment: insights into the progression of this dementing disorder.氧化还原蛋白质组学鉴定阿尔茨海默病和轻度认知障碍中氧化修饰的脑蛋白:对这种痴呆症进展的见解
J Alzheimers Dis. 2007 Aug;12(1):61-72. doi: 10.3233/jad-2007-12107.
7
Roles of amyloid beta-peptide-associated oxidative stress and brain protein modifications in the pathogenesis of Alzheimer's disease and mild cognitive impairment.淀粉样β肽相关氧化应激和脑蛋白修饰在阿尔茨海默病和轻度认知障碍发病机制中的作用。
Free Radic Biol Med. 2007 Sep 1;43(5):658-77. doi: 10.1016/j.freeradbiomed.2007.05.037. Epub 2007 Jun 13.
8
Redox proteomics identification of oxidatively modified hippocampal proteins in mild cognitive impairment: insights into the development of Alzheimer's disease.氧化还原蛋白质组学鉴定轻度认知障碍中氧化修饰的海马体蛋白质:对阿尔茨海默病发展的见解
Neurobiol Dis. 2006 May;22(2):223-32. doi: 10.1016/j.nbd.2005.11.002. Epub 2006 Feb 8.
9
Proteins as biomarkers of oxidative/nitrosative stress in diseases: the contribution of redox proteomics.蛋白质作为疾病中氧化/亚硝化应激的生物标志物:氧化还原蛋白质组学的贡献
Mass Spectrom Rev. 2005 Jan-Feb;24(1):55-99. doi: 10.1002/mas.20006.

氧化还原蛋白质组学。

Redox proteomics.

出版信息

Antioxid Redox Signal. 2012 Dec 1;17(11):1487-9. doi: 10.1089/ars.2012.4742. Epub 2012 Jul 9.

DOI:10.1089/ars.2012.4742
PMID:22671972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3448936/
Abstract

Proteins are major targets of reactive oxygen and nitrogen species (ROS/RNS) and numerous post-translational, reversible or irreversible modifications have been characterized, which may lead to a change in the structure and/or function of the oxidized protein. Redox proteomics is an increasingly emerging branch of proteomics aimed at identifying and quantifying redox-based changes within the proteome both in redox signaling and under oxidative stress conditions. Correlation between protein oxidation and human disease is widely accepted, although elucidating cause and effect remains a challenge. Increasing biomedical data have provided compelling evidences for the involvement of perturbations in redox homeostasis in a large number of pathophysiological conditions and aging. Research toward a better understanding of the molecular mechanisms of a disease together with identification of specific targets of oxidative damage is urgently required. This is the power and potential of redox proteomics. In the last few years, combined proteomics, mass spectrometry (MS), and affinity chemistry-based methodologies have contributed in a significant way to provide a better understanding of protein oxidative modifications occurring in various biological specimens under different physiological and pathological conditions. Hence, this Forum on Redox Proteomics is timely. Original and review articles are presented on various subjects ranging from redox proteomics studies of oxidatively modified brain proteins in Alzheimer disease and animal models of Alzheimer and Parkinson disease, to potential new biomarker discovery paradigm for human disease, to chronic kidney disease, to protein nitration in aging and age-related neurodegenerative disorders, electrophile-responsive proteomes of special relevance to diseases involving mitochondrial alterations, to cardiovascular physiology and pathology.

摘要

蛋白质是活性氧和活性氮物种(ROS/RNS)的主要靶标,已经有许多翻译后、可逆或不可逆的修饰被描述,这些修饰可能导致氧化蛋白的结构和/或功能发生变化。氧化还原蛋白质组学是蛋白质组学中一个新兴的分支,旨在鉴定和定量蛋白质组中氧化还原相关的变化,包括氧化还原信号和氧化应激条件下。虽然阐明因果关系仍然是一个挑战,但蛋白质氧化与人类疾病之间的相关性已被广泛接受。越来越多的生物医学数据为氧化还原稳态失调在大量病理生理条件和衰老中的参与提供了令人信服的证据。为了更好地理解疾病的分子机制并确定氧化损伤的特定靶点,急需开展研究。这就是氧化还原蛋白质组学的力量和潜力。在过去几年中,结合蛋白质组学、质谱(MS)和基于亲和化学的方法学在很大程度上有助于更好地理解在不同生理和病理条件下各种生物样本中发生的蛋白质氧化修饰。因此,这个氧化还原蛋白质组学论坛是及时的。本文论坛涵盖了各种主题的原始和综述文章,范围从阿尔茨海默病氧化修饰脑蛋白的氧化还原蛋白质组学研究和阿尔茨海默病和帕金森病的动物模型,到人类疾病潜在的新生物标志物发现范式,再到慢性肾病、衰老和与年龄相关的神经退行性疾病中的蛋白质硝化、与涉及线粒体改变的疾病特别相关的亲电物响应蛋白质组学,再到心血管生理学和病理学。