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Department of Biochemistry, School of Dentistry [C. L. B., N. B.], and the Department of Surgery (Urology), School of Medicine [N. B.], University of Maryland, Baltimore, Maryland 21201
In the presence of 10 mM molybdate ion, we are able to detect the appearance of a [6,7-3H]-17,21-dimethyl-19-nor-4,9-pregnadiene-3,20-dione- ([3H]R5020) binding moiety in human prostatic cytosol which sedimented at approximately 8S in a glycerol density gradient. The specifically bound [3H]-R5020 was displaced by progesterone, tiramcinolone acetonide, and R5020 but not by cortisol, dihydrotestosterone, 17ß-estradiol, or diethylstilbestrol. Specific binding of [3H]R5020 in the presence of molybdate ion was shown to saturate at 7 x 10-10 M (n = 64 fmol/mg of protein). The optimum concentration of molybdate ion for enhancing specific binding of [3H]-R5020 was determined to be between 7 and 20 mM. Molybdate ion was also effective in stabilizing the 8S R5020-binding moiety in a preincubation for 16 hr at 0° in the absence of added steroid.
1 This work was undertaken in partial fulfillment of research requirements for the University-wide Ph.D. program in biochemistry at the University of Maryland.
2 To whom requests for reprints should be addressed.
Received 10/31/79. Accepted 3/20/80.
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