Ligand Cross-reactivity within the Protease-activated Receptor Family

• Published in: The Journal of biological chemistry Vol. 271; no. 28; pp. 16466 - 16471
• Main Authors: Blackhart, Brian D., Emilsson, Kjell, Nguyen, Dat, Teng, Willy, Martelli, Arnold J., Nystedt, Sverker, Sundelin, Johan, Scarborough, Robert M.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 12.07.1996; American Society for Biochemistry and Molecular Biology
• Subjects: Amino Acid Sequence; Animals; Humans; Ligands; Mice; Molecular Sequence Data; Oligopeptides - pharmacology; Peptide Fragments - pharmacology; Receptor, PAR-2; Receptors, Cell Surface - agonists; Receptors, Cell Surface - genetics; Receptors, Cell Surface - metabolism; Trypsin - pharmacology; Xenopus laevis
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.271.28.16466

Recently, a second member of the protease-activated receptor (PAR) family, named PAR-2, has been identified. Similar to the thrombin receptor, PAR-2 appears to be activated by proteolytic-mediated exposure of a “tethered ligand” sequence and can also be activated by the corresponding synthetic peptides. Similarities in the amino acid sequence of the receptors' tethered ligand sequences suggest that their respective agonist peptides might not be absolutely specific for their particular receptors. To test this, the receptor specificity of each agonist has been determined by measuring the responses of Xenopus oocytes expressing the thrombin receptor or PAR-2 to agonist peptides or enzymes. Thrombin receptors responded to thrombin, the human thrombin receptor-activating peptide SFLLRNP-NH2 (TRAP) (EC50 = 0.1 µM), and Xenopus TRAP, TFRIFD-NH2 (EC50 = 1 µM), but did not show any increase in calcium efflux over control levels with trypsin (50 nM) or PAR-2 agonist peptides (100 µM). Human and murine PAR-2 receptors responded comparably to human and murine PAR-2 agonist peptides (SLIGKVD and SLIGRL, respectively) (EC50 = 0.5-2.0 µM) and trypsin, but not to thrombin. PAR-2 was also found to be responsive to TRAP (EC50 = 1 µM) but was unresponsive to Xenopus TRAP (50 µM). Responses to additional peptide agonist analogs suggest that an amino-terminal serine is critical for PAR-2 agonist activity.