Translational Psychiatry Program, Department of Psychiatry and Behavioral Sciences, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX 77054, USA.
Department of Translational Science in Psychiatry, Max Planck Institute of Psychiatry, 80804 Munich, Germany.
Int J Mol Sci. 2017 Dec 5;18(12):2614. doi: 10.3390/ijms18122614.
Among the chaperones and co-chaperones regulating the glucocorticoid receptor (GR), FK506 binding protein (FKBP) 51 is the most intensely investigated across different disciplines. This review provides an update on the role of the different co-chaperones of Hsp70 and Hsp90 in the regulation of GR function. The development leading to the focus on FKBP51 is outlined. Further, a survey of the vast literature on the mechanism and function of FKBP51 is provided. This includes its structure and biochemical function, its regulation on different levels-transcription, post-transcription, and post-translation-and its function in signaling pathways. The evidence portraying FKBP51 as a scaffolding protein organizing protein complexes rather than a chaperone contributing to the folding of individual proteins is collated. Finally, FKBP51's involvement in physiology and disease is outlined, and the promising efforts in developing drugs targeting FKBP51 are discussed.
在调节糖皮质激素受体 (GR) 的伴侣蛋白和共伴侣蛋白中,FK506 结合蛋白 (FKBP) 51 是不同学科研究最多的蛋白。本文综述了不同 HSP70 和 HSP90 共伴侣在调节 GR 功能中的作用。概述了导致关注 FKBP51 的发展。此外,还对 FKBP51 的机制和功能的大量文献进行了综述。这包括其结构和生化功能、在转录、转录后和翻译后水平的调节及其在信号通路中的功能。还整理了将 FKBP51 作为一种支架蛋白组织蛋白复合物而不是作为折叠单个蛋白的伴侣的证据。最后,概述了 FKBP51 在生理学和疾病中的作用,并讨论了针对 FKBP51 开发药物的有希望的努力。