Lipid Peroxidation and Antioxidant Mechanisms
脂质过氧化和抗氧化机制
基本信息
- 批准号:7682104
- 负责人:
- 金额:$ 142.81万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2005
- 资助国家:美国
- 起止时间:2005-09-12 至 2013-06-30
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
DESCRIPTION (provided by applicant):
Lipid Peroxidation and Antioxidant Mechanisms is a competitive renewal proposal for an NIEHS Program- Project that was funded in September of 2005. Environmental stress and lifestyle play an important role in diseases that contribute significantly to mortality in the U.S. Cigarette smoking, alcohol consumption and poor diet combine with other environmental factors to affect the incidence of several diseases. The formation of oxidants is a hallmark of many of these diseases and lipid peroxidation is a common result of diverse environmental insults. Indeed, oxidative stress has been closely associated with the onset of pathologies as diverse as cancer and cardiovascular disease. The underlying mechanisms linking environmental stresses with disease pathogenesis remain obscure. The studies proposed here will test the hypothesis that the balance of competing oxidation pathways for different lipid substrates governs adaptation to oxidative stress and oxidative injury. The Program Project also directly addresses the hypothesis that protein adduction by lipid peroxidation products alters cellular signaling and modulates diseases linked to oxidative stress. This Program Project includes four research projects and one scientific core facility in a tightly-knit group that will provide important insights into the role that oxidation and antioxidants play in human pathophysiology. Project 1 provides a mechanistic framework for understanding peroxidation profiles and leads the chemistry that provides novel lipid affinity-tags for studying protein-electrophile adducts. Project 2 explores the chemistry and biology of eicosapentaenoic acid (EPA), a fatty acid prominent in fish oil, and explores the hypothesis that EPA oxidation products may contribute significantly to the biological properties of this fatty acid. Project 3 evaluates electrophiles that play critical roles in cell signaling and provides the biological platform for studying lipid affinity tags in whole cells. Project 4 suggests that secondary electrophilic products of lipid peroxidation play critical roles in oxidant-associated molecular pathologies and explores methodologies for identification and analysis of protein adducts of these electrophiles. All of the projects are highly collaborative and are highly dependent on the Lipidomics Analysis scientific core.
BACKGROUND
This is a renewal application of a Program Project Grant by a highly integrated team of investigators, led by Dr. Porter, which was initially funded in 2005. The PPG seeks to continue studies towards the mechanisms of lipid oxidation and the role of lipid-derived electrophiles in biological responses to oxidative stress, using innovative strategies and advanced analytical tools to identify biological targets for lipid-derived electrophiles. Although the original proposal was requested for a 5-year period, and the previous review team unanimously recommended reduction to 3 years, in order to focus on development of tools and analytical strategies and for subsequent use in biological studies. The current application consists of 4 Projects, led by the same investigators as in the original application, and includes 2 Cores, an Administrative Core and a newly added Lipidomics Analytical Core, which replaces the original Mass Spectrometry and Proteomics Core.
PROGRAM AS AN INTEGRATED EFFORT
描述(由申请人提供):
脂质过氧化和抗氧化机制是NIEHS计划的一个有竞争力的更新提案-该项目于2005年9月获得资助。在美国,环境压力和生活方式在导致死亡的疾病中起着重要作用。吸烟、饮酒和不良饮食联合收割机与其他环境因素结合,影响几种疾病的发病率。氧化剂的形成是许多这些疾病的标志,脂质过氧化是各种环境损伤的常见结果。事实上,氧化应激与癌症和心血管疾病等多种病理学的发病密切相关。将环境压力与疾病发病机制联系起来的潜在机制仍然不清楚。这里提出的研究将测试的假设,不同的脂质底物的竞争性氧化途径的平衡控制适应氧化应激和氧化损伤。该计划项目还直接解决了脂质过氧化产物的蛋白质加合改变细胞信号传导和调节与氧化应激相关的疾病的假设。该计划项目包括四个研究项目和一个紧密联系的科学核心设施,将为氧化和抗氧化剂在人类病理生理学中的作用提供重要见解。项目1提供了一个机制的框架,了解过氧化配置文件,并导致化学,提供新的脂质亲和标签研究蛋白质亲电加合物。项目2探讨了二十碳五烯酸(EPA)的化学和生物学,EPA是鱼油中的一种主要脂肪酸,并探讨了EPA氧化产物可能对这种脂肪酸的生物学特性有重要贡献的假设。项目3评估在细胞信号传导中起关键作用的亲电体,并为研究全细胞中的脂质亲和标签提供生物平台。项目4表明,脂质过氧化的次级亲电产物在氧化剂相关的分子病理学中起着关键作用,并探索了鉴定和分析这些亲电体的蛋白质加合物的方法。所有的项目都是高度协作的,并且高度依赖于Lipidomics Analysis的科学核心。
背景
这是一个由波特博士领导的高度一体化的研究团队的计划项目赠款的更新申请,该项目最初于2005年获得资助。PPG旨在继续研究脂质氧化的机制以及脂质衍生的亲电试剂在氧化应激生物反应中的作用,使用创新策略和先进的分析工具来确定脂质衍生的亲电试剂的生物靶点。虽然最初的提案要求为期5年,但前一个审查小组一致建议缩短为3年,以便集中精力开发工具和分析战略,并随后用于生物学研究。目前的申请包括4个项目,由与原始申请相同的研究人员领导,包括2个核心,一个行政核心和一个新增加的脂质组学分析核心,取代了原来的质谱和蛋白质组学核心。
作为一项综合努力,
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Ned Allen Porter其他文献
Ned Allen Porter的其他文献
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{{ truncateString('Ned Allen Porter', 18)}}的其他基金
FREE RADICALS, MEMBRANES AND ENZYME PHOTOACTIVATION
自由基、膜和酶光活化
- 批准号:
7605523 - 财政年份:2006
- 资助金额:
$ 142.81万 - 项目类别:
FREE RADICALS, MEMBRANES AND ENZYME PHOTOACTIVATION
自由基、膜和酶光活化
- 批准号:
7731348 - 财政年份:2006
- 资助金额:
$ 142.81万 - 项目类别: