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J. Biol. Chem., Vol. 265, Issue 11, 6048-6054, 04, 1990
DJ Hryb, MS Khan, NA Romas and W Rosner
Sex hormone-binding globulins (SHBG) is a plasma glycoprotein that binds
certain steroids. It, in turn, binds to a specific receptor on cell
membranes. This work was undertaken to investigate the role of steroids in
the interaction of SHBG with its receptor. Because the probe for the
interaction of SHBG with its receptor is 125I-SHBG, we first showed that
125I-SHBG binds [3H]dihydrotestosterone (DHT) at 4 degrees C and 37 degrees
C with KD values similar to those published previously for pure radioinert
SHBG. 125I-SHBG could be prevented from binding to its receptor by a
variety of steroids whose relative inhibitory activity (dihydrotestosterone
much greater than 2- methoxyestradiol greater than testosterone greater
than estradiol much greater than methyltrienolone greater than cortisol)
was almost identical to their relative ability to bind to SHBG. Because
significant binding of [3H]DHT to the SHBG receptor could not be
demonstrated, steroid inhibition of SHBG binding must be noncompetitive. If
steroids bound to SHBG prevent binding to the SHBG receptor, then liganded
SHBG should have a higher apparent KD for its receptor than unliganded
SHBG. This is the case. The KD was 0.86 +/- 0.25 nM for the high affinity
receptor site using liganded SHBG and 0.19 +/- 0.024 nM for unliganded
SHBG. Thus, only liganded SHBG assumes a conformation that prohibits
interaction with the SHBG receptor. However, when unliganded SHBG was
prebound to its receptor, it retained its ability to bind [3H] DHT. The
model that emerges from these observations is as follows. Unliganded SHBG
can bind either steroids or receptor in a reversible reaction; SHBG bound
to a steroid cannot bind to the receptor, but unliganded SHBG that first
binds to the receptor can subsequently bind steroids.
The control of the interaction of sex hormone-binding globulin with its receptor by steroid hormones
Department of Medicine, St. Luke's/Roosevelt Hospital Center, College of Physicians and Surgeons, Columbia University, New York, New York 10019.
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