Pharmaceutical compositions which inhibit FKBP52-mediated regulation of androgen receptor function and methods of using same
Pharmaceutical compositions that bind to a predicted FK506 Binding Protein 52 (FKBP52) interaction surface on the androgen receptor hormone binding domain, otherwise known as FKBP52 Targeting Agents (FTAs) are provided. These compositions of the present invention are found to specifically recognize the FKBP52 regulatory surface on the androgen receptor and inhibit FKBP52 from functionally interacting with the androgen receptor. Compositions comprising the pharmaceutical composition, as well as methods of use, treatment and screening are also provided.
1. A method of identifying a compound in vitro which inhibits FKBP52-enhanced, androgen receptor (AR)-mediated activity, the method comprising:
a) providing an AR tester cell, the tester cell comprising a murine embryonic fibroblast derived from FKBP-52 deficient mice, the tester cell being transfected with a DNA encoding AR, an AR-responsive reporter plasmid, and a vector encoding a FKBP52 protein;
b) providing a control cell, the control cell comprising the murine embryonic fibroblast derived from FKBP-52 deficient mice, the control cell being transfected with the DNA encoding AR, the AR-responsive reporter plasmid, and a vector that does not encode FKBP-52;
c) contacting the cell of a) and b) with a test compound;
d) contacting the cell of a) and b) with an AR agonist;
e) incubating the cell of a) and b) for a period of time;
f) measuring an amount of AR-responsive reporter expression in a) and b); and
g) comparing the amount of AR-responsive reporter expression in the cell of a) and b),
wherein the test compound is identified as inhibiting FKBP-52-enhanced, AR-mediated activity when the amount of AR-responsive reporter expression in the cell of a) is less than the amount of AR-responsive reporter expression in the cell of b).