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Title: Structure-activity relationship for ETB agonism in truncated endothelin-1 analogs. Author: Saeki T, Ihara M, Fukuroda T, Yano M. Journal: Biochem Int; 1992 Oct; 28(2):305-12. PubMed ID: 1456952. Abstract: The essential part of the ETB-selective agonist N-acetyl-GluAlaValTyrPheAlaHisLeuAspIleIleTrp (N-Ac-4AlaET-1(10-21)) for ETB agonism was studied by single amino acid replacement. Single L-alanine substitutions at positions 14, 17, 20 and 21 and the corresponding D-amino acid substitutions at positions 14 and 16-21 resulted in remarkable decreases in ETB binding activity. Furthermore, these analogs elicited endothelium-dependent vasorelaxation in parallel with ETB binding activity. These data indicate that the amino acid residues of Phe14, Leu17, Ile20 and Trp21 and the backbone structure at Phe14 and His16-Trp21 in ET-1 are important for ETB agonism.[Abstract] [Full Text] [Related] [New Search]