Tuberoinfundibular peptide 39 binds to the parathyroid hormone (PTH)/PTH-related peptide receptor, but functions as an antagonist

The tuberoinfundibular peptide TIP39 [TIP-(1-39)], which exhibits only limi ted amino acid sequence homology with PTH and PTH-related peptide (PTHrP), stimulates cAMP accumulation in cells expressing the PTH2 receptor (PTH2R), but it is inactive at the PTK/ PTHrP receptor (PTH1R). However, when using either I-125-labeled rat [Nle(8.21),Tyr(34)]pTH-(1-34)amide (rPTH) or I-12 5-labeled human [Tyr36]PTHrP-(1-36)amide [PTHrP-(1-36)] for radioreceptor s tudies, TIP-(1-39) bound to LLCPK1 cells stably expressing the PTH1R (HKrk- B7 cells), albeit with weak apparent affinity (243 +/- 52 and 210 +/- 64 nM , respectively). In comparison to the parent peptide, the apparent binding affinity of TIP-(3-39) was about 3-fold higher, and that of TIP-(9-39) was about 5.5-fold higher. However, despite their improved ICS, values at the P TH1R, both truncated peptides failed to stimulate cAMP accumulation in HKrk -B7 cells. In contrast, the chimeric peptide PTHrP-(1-20)/TLP-(23-39) bound to HKrk-B7 cells with affinities of 31 +/- 8.2 and 11 +/- 4.0 nM when usin g radiolabeled rPTH and PTHrP-(1-36), respectively, and it stimulated cAMP accumulation in HKrk-B7 and SaOS-2 cells with potencies (EC50, 1.40 +/- 0.3 and 0.38 +/- 0.12 nM, respectively) and efficacies (maximum levels, 39 +/- 8 and 31 +/- 3 pmol/well, respectively) similar to those of PTH-(1-34) and PTHrP-(1-36). In both cell lines, TIP(9-39) and, to a lesser extent, TIP-( 1-39) inhibited the actions of the three agonists with efficiencies similar to those of [Leu(11),D-Trp(12),Trp(23),Tyr(36)] PTHrP-(7-36)amide, an esta blished PTH1R antagonist. Taken together, the currently available data sugg est that the carboxyl-terminal portion of TIP-(1-39) interacts efficiently with the PTH1R, at sites identical to or closely overlapping those used by PTH-(1-34) and PTHrP-(1-36). The amino-terminal residues of TIP(1-39), howe ver, are unable to interact productively with the PTH1R, thus enabling TIP- (1-39) and some of its truncated analogs to function as an antagonist at th is receptor.