Structure and Function of the Parkinson's disease associated protein LRRK2

帕金森病相关蛋白 LRRK2 的结构和功能

• 批准号: 9892146
• 负责人: Quyen Quoc Hoang
• 金额: $ 12.5万
• 依托单位: INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS
• 依托单位国家: 美国
• 财政年份: 2015
• 资助国家: 美国
• 起止时间: 2015-04-01 至 2021-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9892146
• 关键词: Active Sites; Address; Affect; Area; Binding; Biochemical; Complex; Disease; Drug Targeting; Guanosine Triphosphate Phosphohydrolases; Impairment; LRRK2 gene; Lead; Location; Maps; Molecular Conformation; Mutation; Parkinson Disease; Parkinson' s Disease Pathway; Pathogenesis; Phosphotransferases; Procedures; Process; Proteins; Regulation; Sampling; Site; Structure; Work; biophysical analysis; effective therapy; insight; magnesium ion; therapy development

Project Summary: Here we seek to understand how structure and interactions between the domains of LRRK2 regulate its activities, and also how Parkinson's disease-associated mutations affect these processes. Those areas of study are significant because LRRK2 holds the strongest promise for developing effective treatments for Parkinson's disease (PD), for which there is currently none. Mutations in LRRK2 leading to disease clearly perturb LRRK2 kinase activity; however, the mechanism in doing so is complex as mutation sites remote from the kinase domain also exert similar effects on kinase activity. The major roadblock in unraveling these mechanisms had been the lack of protein samples amenable for detail biochemical and biophysical studies. We have overcome that by developing procedures that yield highly purified samples amenable for detail studies. Here we use these samples to study the structure and function of LRRK2, to tease out how its activities are regulated, and to define its mechanism in disease pathogenesis. The three areas to be investigated in this project are: 1. To determine the effects of PD-associated mutations on the structure and function of the Roc domain of LRRK2. We have shown that the PD-mutation R1441H impairs GTPase activity of the Roc domain of LRRK2. This impairment occurs through distorting the active-site, altering the conformation of the switch regions, or impeding the binding of magnesium ions. 2. To determine the GTPase activation domain of Roc and to define the structural basis for GTPase regulation. We have shown that the Roc domain of LRRK2 has low intrinsic GTPase activity, and we have seen that it could be activated 30-fold by an unknown domain within LRRK2. We will use a combination of biochemical and structural studies to identify and define this activation mechanism. 3. To define global structural interactions between the domains within LRRK2. Mutations are found in various parts of LRRK2, but they all affect kinase activity which can be several domains away from the mutation sites, thus indicating that these domains interact with one another working in concert to exert a common function. We will map the spatial arrangement of all domains within LRRK2 to gain insight into how they work together.

项目总结:

项目成果

Structural and Biochemical Characterization of AidC, a Quorum-Quenching Lactonase with Atypical Selectivity.

• DOI: 10.1021/acs.biochem.5b00499
• 发表时间: 2015-07-21
• 期刊: Biochemistry
• 影响因子: 2.9
• 作者: Mascarenhas R;Thomas PW;Wu CX;Nocek BP;Hoang QQ;Liu D;Fast W
• 通讯作者: Fast W