Structure and Mechanisms of Styrene Monooxygenase

苯乙烯单加氧酶的结构和机制

基本信息

批准号：
7488409
负责人：
George T. Gassner
金额：
$ 22.96万
依托单位：
SAN FRANCISCO STATE UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2007
资助国家：
美国
起止时间：
2007-09-01 至 2011-08-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7488409
关键词：
Accidents Active Sites Adhesives Alkylating Agents Amino Acids Biochemical Carcinogens Catalysis Coenzymes Cytochromes Drug Formulations Drug Metabolic Detoxication Electronics Electrons Elements Ensure Environment Environmental Exposure Environmental Hazards Environmental Pollution Enzymes Evaluation Exposure to Fatty Acids Flavins Flavoproteins Generations Goals Health Human Hydroxylation Individual Iron Irritants Isomerase Kinetics Laboratories Lung Maps Metabolic Metabolic Pathway Metabolism Mixed Function Oxygenases Modeling Nucleotides Oxidoreductase Oxygen Pathway interactions Personal Satisfaction Phenols Plant Resins Plastics Preparation Production Property Range Rate Reaction Refuse Disposal Research Resources Risk Roentgen Rays Role Rubber Series Shipping Ships Societies Staging Structural Protein Structure System Testing Toxin Transportation Universities Work Workplace X ray diffraction analysis X-Ray Crystallography X-Ray Diffraction activation product base chemical synthesis directed evolution electron density enzyme mechanism enzyme structure epoxidase instrumentation microbial microorganism phenylacetic acid protein protein interaction reaction rate styrene oxide

项目摘要

DESCRIPTION (provided by applicant): Styrene is an important component of a wide array of plastic, rubber, and over the counter adhesive products. Over the past century, large-scale industrial and shipping accidents and inappropriate waste disposal practices have caused aquatic and terrestrial environments to become heavily contaminated with monomeric styrene. In the work place, individuals involved in both the formulation and application of styrene-based materials are at the greatest risk of high levels exposure. As a biochemical toxin, styrene induces the activity of iron and flavin-dependent monooxygenases, which catalyze epoxidation and hydroxylation reactions to yield strong alkylating agents and pulmonary irritants such as styrene oxide and vinyl phenols. The long-term objective of our research is to elucidate the structures and mechanisms of the enzymes engaged in the styrene metabolic pathway and to establish a model that allows a more accurate evaluation of the human health risk associated with exposure. Our work will also provide a framework for studies of other metabolic and detoxification pathways, which include the synthesis of toxic or unstable pathway intermediates. The enzymes of the styrene metabolic pathway, styrene monooxygenase, styrene oxide isomerase, and phenacetaldehyde dehydrogenase, have been cloned and will be investigated through mechanistic and structural studies. Styrene monooxygenase will be functionally characterized in our laboratory and structurally characterized through X-ray crystallography by Dr. Amy Rosenzweig's group at Northwestern University. Single-turnover and steady-state kinetic studies will be used to characterize the intermediates involved in the styrene epoxidation reaction and to establish the role of protein-protein interactions in the modulation of reaction rates. A combination of stopped-flow and rapid quench studies will be conducted to establish the mechanisms and efficiency of reactive substrate and coenzyme transport in styrene metabolism. Diffraction quality crystals of styrene monooxygenase will be solved and used to identify active site structures engaged catalysis. This work will result in the first complete structural and mechanistic evaluation of a flavoprotein epoxidase. Elucidation of the enzyme structures and mechanisms engaged in the generation and shuttling of the toxic intermediates during styrene metabolism is an essential step in identifying the health risks associated with human and environmental exposure to monomeric styrene.

描述（由申请人提供）：苯乙烯是多种塑料、橡胶和非处方粘合剂产品的重要成分。在过去的一个世纪里，大规模的工业和航运事故以及不适当的废物处理做法导致水生和陆地环境受到单体苯乙烯的严重污染。在工作场所，参与苯乙烯基材料的配制和应用的个人面临高浓度接触的风险最大。作为一种生化毒素，苯乙烯会诱导铁和黄素依赖性单加氧酶的活性，催化环氧化和羟基化反应，产生强烷化剂和肺部刺激物，例如氧化苯乙烯和乙烯基苯酚。我们研究的长期目标是阐明参与苯乙烯代谢途径的酶的结构和机制，并建立一个模型，以便更准确地评估与接触相关的人类健康风险。我们的工作还将为其他代谢和解毒途径的研究提供一个框架，其中包括有毒或不稳定途径中间体的合成。苯乙烯代谢途径的酶、苯乙烯单加氧酶、苯乙烯氧化物异构酶和苯乙醛脱氢酶已被克隆，并将通过机制和结构研究进行研究。苯乙烯单加氧酶将在我们的实验室进行功能表征，并由西北大学 Amy Rosenzweig 博士的小组通过 X 射线晶体学进行结构表征。单周转和稳态动力学研究将用于表征苯乙烯环氧化反应中涉及的中间体，并确定蛋白质-蛋白质相互作用在反应速率调节中的作用。将进行停流和快速猝灭研究相结合，以确定苯乙烯代谢中反应底物和辅酶转运的机制和效率。苯乙烯单加氧酶的衍射质量晶体将被解析并用于识别参与催化的活性位点结构。这项工作将首次对黄素蛋白环氧酶进行完整的结构和机制评估。阐明苯乙烯代谢过程中有毒中间体的产生和穿梭的酶结构和机制，是确定与人类和环境接触单体苯乙烯相关的健康风险的重要一步。