Biological and conformational evaluation of angiotensin II lactam bridge containing analogues

• Autor(a) principal: Oliveira Junior, Vani Xavier
• Data de Publicação: 2011
• Outros Autores: Fázio, Marcos Antonio [UNIFESP], Silva, Adriana Farias, Campana, Patricia Targon, Pesquero, João Bosco [UNIFESP], Santos, Edson Lucas, Costa-Neto, Cláudio Miguel, Miranda, Antonio [UNIFESP]
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Institucional da UNIFESP
• dARK ID: ark:/48912/0013000003s0k
• Texto Completo: http://dx.doi.org/10.1016/j.regpep.2011.05.015; http://repositorio.unifesp.br/handle/11600/34328
• topic: Angiotensin II; Lactam bridge; SAR; Microphysiometer; SPPS; Circular dichroism

Angiotensin II (All) is the active octapeptide product of the renin enzymatic cascade, which is responsible for sustaining blood pressure. in an attempt to establish the All-receptor-bound conformation of this octapeptide, we designed conformationally constrained analogues by scanning the entire All sequence with an i-(i+2) and i-(i + 3) lactam bridge consisting of an Asp-(Xaa)(n)-Lys scaffold. Most analogues presented low agonistic activity when compared to All in the different bioassays tested. the exceptions are cyclo(0-1a) [Asp(0), endo-(Lys(1a))]-All (1) and [Asp(0), endo-(Lys(1a))]-All (2), both of which showed activity similar to All. Based on peptide 1 and the analogue cyclo(3-5)[Sar(1), Asp(3), Lys(5)]-All characterized by Matsoukas et al., we analyzed the agonistic and antagonistic activities, respectively, through a new monocyclic peptide series synthesized by using the following combinations of residues as bridgehead elements for the lactam bond formation: D- or L-Asp combined with D- or L-Lys or L-Glu combined with L-Orn. Six analogues showed an approximately 20% increase in biological activity when compared with peptide (1) and were equipotent to All. in contrast, six analogues presented antagonistic activity. These results suggest that the position of the lactam bridge is more important than the bridge length or chirality for recognition of and binding to the angiotensin 11 AT1-receptor. (C) 2011 Elsevier B.V. All rights reserved.