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Pharmacological characterization of linear analogues of vasopressin generated by the systematic substitution of positions 1 and 6 by L-amino acids.

Abstract：

:Eighteen linear analogues of [Arg8]vasopressin (AVP) were synthesized by systematically substituting the cysteine residues at positions 1 and 6 with a range of L-amino acids. Screening by competition ligand binding revealed that the combinations of amino acid residues tolerated at these positions was very restricted with respect to retention of vasopressin receptor (VPR) binding. Consequently, only three of the eighteen analogues investigated, [Pro1,Met6]AVP, [Gly1,Met6]AVP and [Phe1,Lys6]AVP, bound to the V1a receptor. Furthermore, these three peptides were all selective for the V1a receptor rather than the V1b, V2 and vasotocin receptors. In addition, although very homologous to the natural agonist, these analogues were in fact antagonists at V1a receptors. These data provide insights into the biophysical requirements at positions 1 and 6 of linear ligands for binding to V1a receptors and furthermore, supply clues to the nature of the receptor:ligand interaction.

journal_name

Biochem Pharmacol

journal_title

Biochemical pharmacology

authors

Howl J,Filer AD,Parslow RA,Kirk CJ,Jurzak M,Smith AI,Wheatley M

doi

10.1016/0006-2952(94)90523-1

subject

Has Abstract

pub_date

1994-04-29 00:00:00

pages

1497-501

issue

9

eissn

0006-2952

issn

1873-2968

pii

0006-2952(94)90523-1

journal_volume

47

pub_type

杂志文章

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