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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:蛋白质是活性氧和氮物种(ROS / RNS)的主要靶标,并且已表征了许多翻译后,可逆或不可逆修饰,这可能导致氧化蛋白质的结构和/或功能发生变化。氧化还原蛋白质组学是蛋白质组学的一个新兴分支,旨在鉴定和量化蛋白质组内氧化还原信号传导和氧化应激条件下基于氧化还原的变化。尽管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提供了令人信服的证据,证明在许多病理生理状况和衰老中,摄动参与了氧化还原稳态。迫切需要进行研究以更好地了解疾病的分子机制,并确定特定的氧化损伤靶标。这就是氧化还原蛋白质组学的力量和潜力。在过去的几年中,蛋白质组学,质谱(MS)和基于亲和化学的方法相结合,以重要的方式为人们更好地理解了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提供了条件。因此,这个氧化还原蛋白质组学论坛是及时的。原始和综述文章涉及多个主题,从阿尔茨海默氏病中氧化修饰的脑蛋白的氧化还原蛋白质组学研究,阿尔茨海默氏症和帕金森氏病的动物模型,到人类疾病的潜在新生物标志物发现范例,到慢性肾脏疾病,再到蛋白质硝化。衰老和与年龄相关的神经退行性疾病,与涉及线粒体改变的疾病,心血管生理学和病理学特别相关的亲电反应蛋白。

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