Schlossmacher Michael G, Shimura Hideki
Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Methods Mol Biol. 2005;301:351-69. doi: 10.1385/1-59259-895-1:351.
The identification of monogenic variants of Parkinson's disease (PD) has provided novel insights into its unknown pathogenesis. As the first protein linked to autosomal-recessive forms of PD, Parkin became a welcome tool to explain biochemical and neuropathological observations that had suggested involvement of the ubiquitin-proteasome system (UPS) in PD. Based on cellular expression studies and biochemical in vitro experiments, several researchers ascribed an E3-type, E2-dependent ubiquitin protein ligase activity to wild-type (but not mutant) Parkin proteins. Although the individual components of the proposed Parkin ubiquitin ligase complex in the normal human brain remain to be identified and the E3 ligase effect of Parkin function has not yet been confirmed in an animal model, the scientific exploration of a protein with several links to the UPS has provided many leads in PD research. This chapter describes assays that the authors have used to examine the cellular and in vitro effects of neural Parkin.
帕金森病(PD)单基因变异的鉴定为其未知的发病机制提供了新的见解。作为首个与常染色体隐性遗传形式的PD相关的蛋白质,Parkin成为了解释泛素-蛋白酶体系统(UPS)参与PD的生化和神经病理学观察结果的有用工具。基于细胞表达研究和体外生化实验,一些研究人员将E3型、E2依赖性泛素蛋白连接酶活性归因于野生型(而非突变型)Parkin蛋白。尽管正常人类大脑中拟议的Parkin泛素连接酶复合物的各个成分仍有待确定,且Parkin功能的E3连接酶效应尚未在动物模型中得到证实,但对一种与UPS有多种联系的蛋白质的科学探索为PD研究提供了许多线索。本章描述了作者用于检测神经Parkin的细胞和体外效应的实验方法。