Srj. Hoare et Tb. Usdin, Molecular mechanisms of ligand recognition by parathyroid hormone 1 (PTH1)and PTH2 receptors, CUR PHARM D, 7(8), 2001, pp. 689-713
The mammalian parathyroid hormone (PTH) / PTH receptor family includes PTH1
and PTH2 receptors and three related ligands (PTH, PTH-related protein (PT
HrP) and tuberoinfundibular peptide of 39 residues (TIP39)). Here we compar
atively and systematically review the pharmacological properties of PTH rec
eptors and ligands, structure of the ligands, and molecular mechanisms of r
eceptor-ligand interaction. The PTH1 receptor is activated by PTH and PTHrP
but not by TIP39. The PTH2 receptor is activated by TIP39 but not by PTHrP
. PTH strongly activates the human PTH2 receptor but is a weak partial agon
ist for rat and zebrafish PTH2 receptors. Receptor-G-protein interaction in
creases the receptor binding selectivity of PTHrP and TIP39. Despite differ
ent primary structures, the secondary structures of PTH, PTHrP and TIP39 ar
e quite similar. Each ligand contains an N-terminal and a C-terminal a-heli
x in secondary structure-inducing conditions. Receptor-bound ligand structu
re is less well-characterized. The orientation of receptor-ligand interacti
on is highly similar for PTH and PTHrP binding to the PTH1 receptor and TIP
39 interaction with the PTH2 receptor. Ligands bind according to a 'two-sit
e' mechanism, in which the C-terminal portion of the ligand binds the extra
cellular N-terminal domain of the receptor (N-interaction), and the N-termi
nal ligand portion binds to the juxtamembrane receptor domain (J-interactio
n), The N-interaction provides most of the PTH1-receptor binding energy for
PTH and PTHrP but provides less energy for PTH2 receptor-TIP39 interaction
. The J-interaction stimulates G-protein activation. For the PTH-PTH1 recep
tor interaction, the efficacy-generating component of the J-interaction is
independent of the N-domain of the receptor and C-terminal portion of the l
igand. This finding suggests that it might be possible to design low molecu
lar-weight PTH1 receptor agonists, which could be bone anabolic agents and
used for the treatment of osteoporosis.