权益分类	功能权益	普通用户	{{item.name}}会员
{{category.name}}	{{benefitItem.name}}

Probing the Enzymatic Basis of Canavan Disease

探讨卡纳万病的酶学基础

基本信息

批准号：
7577493
负责人：
RONALD Edward VIOLA
金额：
$ 22.1万
依托单位：
UNIVERSITY OF TOLEDO
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：
2005-02-15 至 2011-01-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7577493
关键词：
Acetyltransferase Active Sites Address Affect Amino Acids Animal Model Aspartate Aspartoacylase Binding Biological Assay Brain Canavan Disease Cell Culture Techniques Cessation of life Classification Clinical Complex Crystallization DNA Data Collection Defect Development Disease Enzyme Inhibitor Drugs Enzyme Inhibitors Enzymes Equilibrium Event Genes Goals Human Individual Ions Knowledge Laboratories Lead Learning Libraries Life Ligands Maps Metabolic Metals Methods Modification Motor Skills Muscle Mutation N-acetylaspartate Neurodegenerative Disorders Patients Phosphorylation Physiological Play Point Mutation Positioning Attribute Post-Translational Protein Processing Property Regulation Relative (related person)Research Personnel Resolution Role Series Site Specificity Structure Substrate Specificity Symptoms System Techniques Testing Variant Viola X ray diffraction analysis X-Ray Diffraction Yeasts analog aspartate N-acetyltransferase base cold temperature cryogenics effective therapy enzyme activity enzyme structure enzyme substrate analog glycosylation improved infancy inhibitor/antagonist interest mutant prevent programs response solid solution

项目摘要

DESCRIPTION (provided by applicant): Canavan disease is a fatal neurodegenerative disorder caused by defects in the acy2 gene that encodes for the enzyme aspartoacylase, thus resulting in abnormally high levels of A/-acetylaspartate (NAA). Symptoms of this disorder, including loss of motor skills and muscle control, appear in early infancy and typically progress very rapidly, with death usually occurring within the first years of life. DNA taken from patients has identified numerous mutations that result in defective aspartoacylase, however, there have been no systematic studies of how and why these alterations affect catalytic activity, and little detailed characterization of aspartoacylase. The goals for this project are to determine the specificity and the detailed mechanism of human aspartoacylase and also the enzyme responsible for the synthesis of NAA in the brain, aspartate A/-acetyltransferase. We will examine how the activities of these enzymes are regulated, identify and define the roles of critical active site amino acids, and synthesize and screen selective inhibitors of aspartate A/-acetyltransferase. The long-range objectives are to use the basic knowledge that we will learn about these enzymes to help overcome the metabolic defects of aspartoacylase in humans. To accomplish these goals we will develop improved expression systems and optimized purification methods for these enzymes. The role of metal ions in aspartoacylase will be examined, and the function of regulatory sites will be assessed by controlled posttranslational modifications and by site-specific covalent modifications. The high-resolution structures of human aspartoacylase and aspartate /V-acetyltransferase will be determined by X-ray diffraction methods, along with the structures of selected active site and regulatory site mutants and enzyme-inhibitor complexes. The coordination application of these techniques in our laboratory will provide a detailed picture of the mechanism and inhibition of aspartate A/-acetyltransferase. We will also learn how aspartoacylase functions, and why it malfunctions in Canavan disease.

描述（由申请人提供）：卡纳万病是一种致命的神经退行性疾病，由编码酶乙酰基酰化酶的acy 2基因缺陷引起，从而导致异常高水平的N-乙酰天冬氨酸（NAA）。这种疾病的症状，包括运动技能和肌肉控制的丧失，出现在婴儿早期，通常进展非常迅速，死亡通常发生在生命的最初几年。从患者身上提取的DNA已经鉴定出许多导致β-酰化酶缺陷的突变，然而，还没有系统的研究这些改变如何以及为什么影响催化活性，并且很少有β-酰化酶的详细表征。该项目的目标是确定人乙酰化酶的特异性和详细机制，以及负责脑中NAA合成的酶，天冬氨酸A/-乙酰转移酶。我们将研究这些酶的活性是如何调节的，确定和定义关键活性位点氨基酸的作用，合成和筛选天冬氨酸A/-乙酰转移酶的选择性抑制剂。长期目标是利用我们将了解的关于这些酶的基本知识来帮助克服人类中的β-酰化酶的代谢缺陷。为了实现这些目标，我们将开发这些酶的改进的表达系统和优化的纯化方法。金属离子的作用，在β-酰化酶将被检查，和监管网站的功能将通过控制翻译后修饰和位点特异性共价修饰进行评估。将通过X-射线衍射方法确定人乙酰化酶和天冬氨酸/V-乙酰转移酶的高分辨率结构，沿着选定的活性位点和调节位点突变体和酶抑制剂复合物的结构。这些技术在本实验室的协同应用将为天冬氨酸A/-乙酰转移酶的作用机制和抑制提供详细的图像。我们还将了解乙酰化酶如何发挥作用，以及为什么它在卡纳万病中出现故障。