The Prospect of FKBP51 as a Drug Target

被引:83
作者
Schmidt, Mathias V. [1 ]
Paez-Pereda, Marcelo [1 ]
Holsboer, Florian [1 ]
Hausch, Felix [1 ]
机构
[1] Max Planck Inst Psychiat, D-80804 Munich, Germany
关键词
chaperones; drug discovery; FK506; immunophilin; psychiatric disorders; GROWTH-FACTOR INDEPENDENCE; GLUCOCORTICOID-RECEPTOR; IDIOPATHIC MYELOFIBROSIS; FK506-BINDING PROTEIN; TREATMENT RESPONSE; PERIPHERAL-BLOOD; CHILDHOOD TRAUMA; SQUIRREL-MONKEY; HPA AXIS; NONIMMUNOSUPPRESSIVE IMMUNOPHILIN;
D O I
10.1002/cmdc.201200137
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The FK506 binding protein 51 (FKBP51) is best known as an Hsp90-associated co-chaperone that regulates the responsiveness of steroid hormone receptors. In human genetic association studies, FKBP51 has repeatedly been associated with emotion processing and numerous stress-related affective disorders. It has also been implicated in contributing to the glucocorticoid hyposensitivity observed in New World primates. More recently, several research groups have consistently shown a protective effect of FKBP51 knockout or knockdown on stress endocrinology and stress-coping behavior in animal models of depression and anxiety. The principal druggability of FKBP51 is exemplified by the prototypic FKBP ligands FK506 and rapamycin. Moreover, FKBP51 is highly suited for X-ray co-crystallography, which should facilitate the rational drug design of improved FKBP51 ligands. In summary, FKBP51 has emerged as a promising new drug target for stress-related disorders that should be amenable to drug discovery.
引用
收藏
页码:1351 / 1359
页数:9
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