Mechanistic Studies of Alkyl Hydroperoxide Reductase and Related Redox Proteins

烷基过氧化氢还原酶及相关氧化还原蛋白的机理研究

• 批准号: 8470170
• 负责人: LESLIE B POOLE
• 金额: $ 38.12万
• 依托单位: WAKE FOREST UNIVERSITY HEALTH SCIENCES
• 依托单位国家: 美国
• 财政年份: 1993
• 资助国家: 美国
• 起止时间: 1993-12-01 至 2016-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8470170
• 关键词: Accounting; Active Sites; Aging; Antibiotics; Antioxidants; Apoptosis; Area; Bacteria; Basic Science; Binding; Biological Assay; Biology; C-terminal; Catalysis; Cell Signaling Process; Cells; Communicable Diseases; Complex; Confocal Microscopy; Cysteine; Data; Degenerative Disorder; Development; Diffusion; Disease; Embryo; Environment; Enzymatic Biochemistry; Enzymes; Eukaryota; Eukaryotic Cell; Event; Family; Fibroblasts; Floods; Fluorescent Probes; Generations; Goals; Grant; Growth Factor; Hour; Human; Hydrogen Peroxide; Immune system; Immunofluorescence Microscopy; Impairment; Infectious Agent; Knockout Mice; Laboratories; Left; Ligand Binding; Ligands; Malignant Neoplasms; Measures; Mediating; Modeling; Modification; Mutagenesis; Oral cavity; Organism; Output; Oxidants; Oxidation-Reduction; Oxidative Regulation; Oxidative Stress; Pathway interactions; Peroxidases; Peroxides; Phenotype; Physiological; Platelet-Derived Growth Factor; Play; Point Mutation; Post-Translational Protein Processing; Prevention; Property; Protein Isoforms; Proteins; Reactive Oxygen Species; Reagent; Relative (related person); Research; Resistance; Role; Salmonella typhimurium; Science; Second Messenger Systems; Signal Transduction; Signaling Molecule; Site; Specificity; Staging; Structure; Substrate Specificity; Sulfinic Acids; TNF gene; Testing; Therapeutic Agents; Therapeutic Human Experimentation; Toll-like receptors; Toxin; Treponema pallidum; Tumor Necrosis Factor-alpha; Variant; Vertebrates; Zebrafish; alkyl hydroperoxide reductase; analog; base; catalase; cell growth regulation; combat; cysteine sulfinic acid; cysteinesulfenic acid; cytokine; design; disulfide bond; follow-up; glutathione peroxidase; human disease; in vivo; inhibitor/antagonist; interest; killings; knock-down; mathematical model; migration; mutant; novel therapeutics; oxidation; oxidative damage; pathogen; pathogenic bacteria; prevent; public health relevance; research study; second messenger; vector

DESCRIPTION (provided by applicant): Hydrogen peroxide is a toxin used by the human immune system to kill infectious organisms, and increasing evidence shows that it is also a common second messenger in eukaryotic signaling. In humans, cytokines, growth factors and toll-like receptors of the innate immune system are thought to signal via hydrogen peroxide. Catalase and glutathione peroxidase have long been viewed as the major enzymes degrading peroxide in cells, however, over the past few years, a distinct, highly abundant family of peroxide- reducing enzymes, peroxiredoxins (Prxs), have moved from relative obscurity to become a major focus of redox biology research. The peroxidase activity of eukaryotic Prxs was overlooked for many years, because those Prxs that are highly expressed in eukaryotes are easily inactivated by peroxide. We have developed expertise in Prx enzymology over more than 15 years of characterizing of Prxs from pathogenic bacteria (e.g. Salmonella typhimurium AhpC). These Prxs are targets for antibiotic development because of the role they play in protecting the bacteria from the human immune system. In 2003, our structural and functional studies on S. typhimurium AhpC led us to discover the structural basis for the sensitivity toward peroxides that is conserved for a subset of Prxs that are highly expressed across all eukarya (this is the basis for the structural hypothesis that underlies the present grant, which dictates that the mobility of proximal secondary structures packing near the active site is a key determinant of the sensitivity of Prxs to overoxidation by peroxides and of the ability of Prxs to act as antioxidants). We further proposed the "floodgate hypothesis" for how this sensitivity to inactivation would actually be beneficial in organisms where hydrogen peroxide is being used as a signaling molecule, so that the antioxidant properties of the Prxs could be switched off under appropriate conditions to allow for a controlled burst in peroxide levels. Given the importance of Prxs both in pathogen defense and in human cells for combating oxidative stress and for cellular regulation, we propose here to identify the key determinants of sensitivity toward overoxidation and of efficient antioxidant function by investigating the conformational "mobility" of a few carefully chosen proteins and mutants; relevant rates constants within the catalytic cycle and inactivation pathways for these proteins will also be examined (Aim 1). In Aim 2, we will identify structural features around the highly conserved active site of Prxs which are important for binding and reduction of distinct hydroperoxide substrates. In Aim 3, we will determine whether or not the sensitivity of Prxs toward inactivation by peroxides during turnover (the "floodgate") is critical to modulating the levels of H2O2 generated during cell signaling events through cell-based studies of Prx functions.

描述（由申请人提供）：过氧化氢是一种由人体免疫系统用于杀死感染性生物的毒素，越来越多的证据表明，它也是真核生物信号传导中常见的第二信使。在人类中，先天免疫系统的细胞因子、生长因子和toll样受体被认为通过过氧化氢发出信号。过氧化氢酶和谷胱甘肽过氧化物酶一直被认为是降解细胞中过氧化物的主要酶，然而，在过去的几年中，一个独特的，高度丰富的过氧化物还原酶家族，过氧化物还原酶（Prxs），已经从相对默默无闻的发展成为氧化还原生物学研究的主要焦点。真核生物中高表达的Prxs很容易被过氧化物酶灭活，因此其过氧化物酶活性多年来一直被忽视。我们在Prx酶学方面拥有超过15年的专业知识，用于表征来自病原菌（例如鼠伤寒沙门氏菌AhpC）的Prx。这些Prx是抗生素开发的目标，因为它们在保护细菌免受人类免疫系统侵害方面发挥着作用。2003年，我们对S.鼠伤寒杆菌AhpC使我们发现了对过氧化物敏感的结构基础，这种敏感性在所有真核细胞中高度表达的Prx亚群中是保守的（这是构成本补助金的结构性假设的基础，这表明，活性位点附近的近端二级结构的流动性是Prxs对过氧化物过氧化的敏感性以及Prxs在过氧化物过氧化反应中的能力的关键决定因素。作为抗氧化剂）。我们进一步提出了“闸门假说”，即这种对失活的敏感性实际上在过氧化氢被用作信号分子的生物体中是如何有益的，这样Prxs的抗氧化特性就可以在适当的条件下被关闭，以允许过氧化物水平的受控爆发。考虑到Prxs在病原体防御和人类细胞中对抗氧化应激和细胞调节的重要性，我们在这里提出通过研究一些精心选择的蛋白质和突变体的构象“移动性”来确定对过氧化敏感性和有效抗氧化功能的关键决定因素;还将检查这些蛋白质的催化循环和失活途径中的相关速率常数（目标1）。在目标2中，我们将确定Prxs的高度保守的活性位点周围的结构特征，这对于不同的氢过氧化物底物的结合和还原是重要的。在目标3中，我们将通过基于细胞的Prx功能研究，确定Prx对周转期间过氧化物失活（“闸门”）的敏感性是否对调节细胞信号传导事件期间产生的H2 O2水平至关重要。

项目成果

Backbone chemical shift assignments for Xanthomonas campestris peroxiredoxin Q in the reduced and oxidized states: a dramatic change in backbone dynamics.

• DOI: 10.1007/s12104-015-9637-8
• 发表时间: 2016-04
• 期刊: Biomolecular NMR assignments
• 影响因子: 0.9
• 作者: Buchko GW;Perkins A;Parsonage D;Poole LB;Karplus PA
• 通讯作者: Karplus PA

Peroxiredoxins as molecular triage agents, sacrificing themselves to enhance cell survival during a peroxide attack.

• DOI: 10.1016/j.molcel.2012.01.012
• 发表时间: 2012-02-10
• 期刊: MOLECULAR CELL
• 影响因子: 16
• 作者: Karplus, P. Andrew;Poole, Leslie B.
• 通讯作者: Poole, Leslie B.

Measurement of peroxiredoxin activity.

• DOI: 10.1002/0471140856.tx0710s49
• 发表时间: 2011-08
• 期刊: Current protocols in toxicology
• 作者: Nelson, Kimberly J;Parsonage, Derek
• 通讯作者: Parsonage, Derek

Strained cycloalkynes as new protein sulfenic acid traps.

• DOI: 10.1021/ja500364r
• 发表时间: 2014-04-30
• 期刊: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
• 影响因子: 15
• 作者: Poole, Thomas H.;Reisz, Julie A.;Zhao, Weiling;Poole, Leslie B.;Furdui, Cristina M.;King, S. Bruce
• 通讯作者: King, S. Bruce

Identification of a new gene responsible for the oxygen tolerance in aerobic life of Streptococcus mutans.

鉴定负责变形链球菌有氧生活中氧耐受性的新基因。

• DOI: 10.1271/bbb.64.1106
• 发表时间: 2000
• 期刊: Bioscience, biotechnology, and biochemistry
• 作者: Yamamoto,Y;Higuchi,M;Poole,LB;Kamio,Y
• 通讯作者: Kamio,Y