Hartson Steven D, Matts Robert L
Department of Biochemistry and Molecular Biology, Oklahoma State University, Stillwater, OK, USA.
Biochim Biophys Acta. 2012 Mar;1823(3):656-67. doi: 10.1016/j.bbamcr.2011.08.013. Epub 2011 Aug 27.
Hsp90 is the target of ongoing drug discovery studies seeking new compounds to treat cancer, neurodegenerative diseases, and protein folding disorders. To better understand Hsp90's roles in cellular pathologies and in normal cells, numerous studies have utilized proteomics assays and related high-throughput tools to characterize its physical and functional protein partnerships. This review surveys these studies, and summarizes the strengths and limitations of the individual attacks. We also include downloadable spreadsheets compiling all of the Hsp90-interacting proteins identified in more than 23 studies. These tools include cross-references among gene aliases, human homologues of yeast Hsp90-interacting proteins, hyperlinks to database entries, summaries of canonical pathways that are enriched in the Hsp90 interactome, and additional bioinformatic annotations. In addition to summarizing Hsp90 proteomics studies performed to date and the insights they have provided, we identify gaps in our current understanding of Hsp90-mediated proteostasis. This article is part of a Special Issue entitled: Heat Shock Protein 90 (HSP90).
热休克蛋白90(Hsp90)是当前药物研发研究的靶点,这些研究旨在寻找治疗癌症、神经退行性疾病和蛋白质折叠紊乱的新化合物。为了更好地理解Hsp90在细胞病变和正常细胞中的作用,众多研究利用蛋白质组学分析及相关高通量工具来表征其物理和功能上的蛋白质伙伴关系。本综述对这些研究进行了概述,并总结了各项研究的优缺点。我们还提供了可下载的电子表格,汇总了23项以上研究中鉴定出的所有与Hsp90相互作用的蛋白质。这些工具包括基因别名之间的交叉引用、酵母Hsp90相互作用蛋白的人类同源物、指向数据库条目的超链接、Hsp90相互作用组中富集的经典信号通路总结以及其他生物信息学注释。除了总结迄今为止进行的Hsp90蛋白质组学研究及其提供的见解之外,我们还指出了目前对Hsp90介导的蛋白质稳态理解中的空白。本文是名为“热休克蛋白90(HSP90)”的特刊的一部分。