Enzymic Detoxification for Organophosphate Nerve Agents
有机磷神经毒剂的酶解毒
基本信息
- 批准号:8114985
- 负责人:
- 金额:$ 29.55万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2003
- 资助国家:美国
- 起止时间:2003-07-01 至 2013-06-30
- 项目状态:已结题
- 来源:
- 关键词:Active SitesAgricultureAmino Acid SequenceChemical WeaponsCholinesterasesCollaborationsDecontaminationDetectionDiffusionDrug Metabolic DetoxicationEngineeringEnzymesEscherichia coliEstersHealthHumanHydrolysisInsecticidesLeftLibrariesMeasurementMethodsModificationMutagenesisOrganophosphatesParaoxonPhosphoric Triester HydrolasesPoisonProceduresPropertyProteinsProtocols documentationReportingResearchResolutionSarinScreening procedureSiteSocietiesSomanSpectrum AnalysisStereoisomerStructureSystemTechniquesVariantX ray diffraction analysisX-Ray CrystallographyX-Ray Diffractionanalogbasecatalystcombinatorialcyclosarindesigndesign and constructiondirected evolutionenzyme activityenzyme structurehigh throughput screeninginorganic phosphatemolecular recognitionmutantnerve agentneurotransmissionnoveltabunthree dimensional structure
项目摘要
DESCRIPTION (provided by applicant): Organophosphate and organophosphonate esters are among the most toxic compounds that have ever been synthesized. These compounds are toxic because of their inherent ability to interfere with nerve transmission through the rapid and irreversible inactivation of the enzyme acetyl cholinesterase. The toxic properties of the organophosphates have been exploited as agricultural insecticides and as chemical weapons. A bacterial phosphotriesterase enzyme has been identified that can function as a catalyst for the recognition, hydrolysis, and detoxification of a broad spectrum of organophosphate nerve agents. The primary objective of this application is to design and characterize modified forms of the bacterial phosphotriesterase that are optimized for the selective recognition and destruction of those organophosphates that pose the most serious threats to human health. Rational and combinatorial libraries of mutant enzymes will be constructed and those variants with enhanced catalytic proficiency will be identified through novel screening and selection procedures. The progressive changes in the amino acid sequence of the bacterial phosphotriesterase will be directly correlated with the enhancements in the catalytic constants and the modifications within the active site as determined by X-ray diffraction methods. PUBLIC HEALTH RELEVANCE: The toxic properties of the organophosphate nerve agents represent a serious threat to the health and well being of civilized societies. The primary objective of this project is to create novel catalytic enzymes that are optimized in their ability to detect, destroy and detoxify a broad spectrum of organophosphate nerve agents.
描述(由申请人提供):有机磷酸盐和有机膦酸酯是有史以来合成的毒性最强的化合物之一。这些化合物是有毒的,因为它们固有的能力,通过快速和不可逆的乙酰胆碱酯酶失活干扰神经传递。有机磷的毒性已被用作农业杀虫剂和化学武器。细菌磷酸三酯酶已被确定,可以作为一个催化剂的识别,水解和解毒广泛的有机磷神经毒剂。本应用程序的主要目的是设计和表征细菌磷酸三酯酶的修饰形式,该形式优化为选择性识别和破坏那些对人类健康构成最严重威胁的有机磷酸盐。将构建合理的和组合的突变酶文库,并通过新的筛选和选择程序确定具有增强催化能力的变体。细菌磷酸三酯酶氨基酸序列的进行性变化与催化常数的增强和活性位点内的修饰直接相关。公共卫生相关性:有机磷神经毒剂的毒性对文明社会的健康和福祉构成严重威胁。该项目的主要目标是创造新的催化酶,优化其检测、破坏和解毒广泛的有机磷神经毒剂的能力。
项目成果
期刊论文数量(14)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Detoxification of organophosphate nerve agents by bacterial phosphotriesterase.
- DOI:10.1016/j.taap.2005.02.025
- 发表时间:2005-09-01
- 期刊:
- 影响因子:3.8
- 作者:Ghanem, Eman;Raushel, Frank M
- 通讯作者:Raushel, Frank M
Catalytic mechanisms for phosphotriesterases.
- DOI:10.1016/j.bbapap.2012.04.004
- 发表时间:2013-01
- 期刊:
- 影响因子:3.2
- 作者:Bigley, Andrew N.;Raushel, Frank M.
- 通讯作者:Raushel, Frank M.
Enzymes for the homeland defense: optimizing phosphotriesterase for the hydrolysis of organophosphate nerve agents.
- DOI:10.1021/bi300811t
- 发表时间:2012-08-14
- 期刊:
- 影响因子:2.9
- 作者:Tsai PC;Fox N;Bigley AN;Harvey SP;Barondeau DP;Raushel FM
- 通讯作者:Raushel FM
Control of stereoselectivity in phosphotriesterase.
磷酸三酯酶立体选择性的控制。
- DOI:10.1016/s0076-6879(04)88022-4
- 发表时间:2004
- 期刊:
- 影响因子:0
- 作者:Hong,Suk-Bong;Raushel,FrankM
- 通讯作者:Raushel,FrankM
Enzymatic neutralization of the chemical warfare agent VX: evolution of phosphotriesterase for phosphorothiolate hydrolysis.
- DOI:10.1021/ja402832z
- 发表时间:2013-07-17
- 期刊:
- 影响因子:15
- 作者:Bigley, Andrew N.;Xu, Chengfu;Henderson, Terry J.;Harvey, Steven P.;Raushel, Frank M.
- 通讯作者:Raushel, Frank M.
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Frank M. Raushel其他文献
Catalytic detoxification
催化解毒
- DOI:
10.1038/469310a - 发表时间:
2011-01-19 - 期刊:
- 影响因子:48.500
- 作者:
Frank M. Raushel - 通讯作者:
Frank M. Raushel
The use of phosphotriesterase in the synthesis of enantiomerically pure ProTide prodrugs
磷酸三酯酶在合成对映体纯的前药ProTide中的应用
- DOI:
10.1016/j.cbi.2025.111597 - 发表时间:
2025-09-05 - 期刊:
- 影响因子:5.400
- 作者:
Andrew N. Bigley;Frank M. Raushel - 通讯作者:
Frank M. Raushel
Frank M. Raushel的其他文献
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{{ truncateString('Frank M. Raushel', 18)}}的其他基金
The Discovery of Novel Metabolic Pathways for the Biosynthesis and Degradation of Complex Carbohydrates within the Human Gut Microbiome
人类肠道微生物组内复杂碳水化合物生物合成和降解的新代谢途径的发现
- 批准号:
10323657 - 财政年份:2021
- 资助金额:
$ 29.55万 - 项目类别:
The Discovery of Novel Metabolic Pathways for the Biosynthesis and Degradation of Complex Carbohydrates within the Human Gut Microbiome
人类肠道微生物组内复杂碳水化合物生物合成和降解的新代谢途径的发现
- 批准号:
10557076 - 财政年份:2021
- 资助金额:
$ 29.55万 - 项目类别:
The Discovery of Novel Metabolic Pathways for the Biosynthesis and Degradation of Complex Carbohydrates within the Human Gut Microbiome
人类肠道微生物组内复杂碳水化合物生物合成和降解的新代谢途径的发现
- 批准号:
10084621 - 财政年份:2021
- 资助金额:
$ 29.55万 - 项目类别:
Novel Biochemical Pathways for the Metabolism of Carbohydrates in the Human gut Micriobiome
人类肠道微生物组中碳水化合物代谢的新生化途径
- 批准号:
10063528 - 财政年份:2017
- 资助金额:
$ 29.55万 - 项目类别:
Deciphering Enzyme Specificity: Amidohydrolase Superfamily
破译酶的特异性:酰胺水解酶超家族
- 批准号:
7743893 - 财政年份:2009
- 资助金额:
$ 29.55万 - 项目类别:
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