PROBING THE V-1A VASOPRESSIN RECEPTOR-BINDING SITE WITH PYROGLUTAMATE-SUBSTITUTED LINEAR ANTAGONISTS

We have synthesized eight analogues of the linear vasopressin antagoni st (3)-Gln(4)-Asn(5)-Arg(6)-Pro(7)-Arg(8)-Tyr(NH2)(9) substituted with L-, or D-, pyroglutamate at position-1, Asn or Val at position-4 and Arg or Met at position 6. All of these peptides bound to the V-1a vaso pressin receptor with affinities ranging 33.6-5, 470 nM. Of this serie s, only two peptides, [LpGlu(1)Val(4)Arg(6)Tyr(NH2)(9)]AVP K-d = 48.4 nM and [DpGlu(1)Val(4)Arg(6)Tyr(NH2)(9)]AVP K-d = 691 nM, bound to the V-2 vasopressin receptor. All of the neurohypophysial hormone recepto rs studied (V-1a VPR, V-2 VPR and OTR) were found to be stereoselectiv e with respect to the N-terminal pGlu residue. The effect on binding c haracteristics of L-pGlu(1) and D-pGlu(1) analogues was dependent on b oth the sequence of the peptide and on the receptor subtype in questio n. From these data we found that peptide 5, which has the structure Dp Glu-DTyr(Et)-Phe-Val-Asn-Arg-Pro-Arg-Tyr(NH2), exhibited the highest V -1a/OTR selectivity reported to date (V-1a VPR K-d = 82 nM; OTR no bin ding at 10 mu M). As such, peptide 5 will provide useful leads to the development of ligands with enhanced V-1a/OTR selectivity. The binding affinity and hydrophobicity of pyroglutamate-substituted peptides was compared with previously characterized V-1a receptor antagonists whic h contained a range of position-1 substitutions. The hydrophobicity of both cyclic and linear antagonists was markedly increased relative to the agonists AVP and [Phe(2)Om(8)]VT but increased hydrophobicity alo ne did not exclusively lead to high affinity antagonists. Data present ed support the contention that in addition to a general increase in hy drophobicity/lipophilicity, position-1 influences the pharmacophore of vasopressin antagonists by providing molecular determinants for ligan d/receptor interaction.