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Redox proteomics

机译:氧化还原蛋白质组学

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摘要

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.
机译:蛋白质是反应性氧和氮物质(ROS / RNS)的主要靶标,表征了许多翻译后,可逆或不可逆的修饰,这可能导致氧化蛋白的结构和/或功能的变化。氧化还原蛋白质组学是蛋白质组学的越来越新的蛋白质组学分支,旨在鉴定和定量蛋白质组内的氧化还原的变化,氧化还原信号传导和氧化应激条件下。蛋白质氧化与人类疾病之间的相关性被广泛接受,尽管阐明的原因和效果仍然是一个挑战。增加的生物医学数据已经为在大量病理生理病症和老龄化中涉及雷诺稳态扰动的涉及令人信服的证据。迫切需要研究更好地了解疾病的分子机制,迫切需要鉴定鉴定氧化损伤的特定氧化损伤靶标。这是氧化还原蛋白质组学的力量和潜力。在过去几年中,组合蛋白质组学,质谱(MS)和亲和力化学的方法有助于提供在不同生理和病理条件下各种生物标本中发生的蛋白质氧化修饰的更好理解。因此,这个关于氧化还原蛋白质组学论坛的论坛是及时的。原始和复习文章介绍了氧化铈改性脑蛋白在阿尔茨海默病和帕金森病的动物模型中的氧化还原蛋白质组学研究的各种科目,以潜在的人类疾病的新生物标志物发现范式,慢性肾病,蛋白质硝化衰老和年龄相关的神经退行性疾病,电泳响应蛋白质与涉及线粒体改变的疾病的特殊相关性,以心血管生理学和病理学。

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