A conformation-activity study of the [L-(alpha Me)Phe]3 analog of the formyl methionyl tripeptide chemoattractant

C. Toniolo, M. Crisma, S. Pegoraro, G. Valle, G.M. Bonora, E.L. Becker, S. Polinelli, W.H.J. Boesten, H.E. Schoemaker, E.M. Meijer

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35 Citations (Scopus)

Abstract

CHO-L-Met-L-Leu-L-(alpha Me)Phe-OMe, an analog of the formyl methionyl tripeptide chemoattractant CHO-L-Met-L-Leu-L-Phe-OH, was synthesized by solution methods and fully characterized. This compound was prepared to determine the effect of the incorporation of a conformationally restricted C alpha,alpha-disubstituted alpha-amino acid residue at position 3 on the relation of three-dimensional structure to biological activity. The peptide was tested for its ability to induce granule enzyme secretion from rabbit peritoneal polymorphonuclear leukocytes. In parallel, a conformational analysis was performed in the crystal state by x-ray diffraction and in organic solution by infrared absorption and 1H nuclear magnetic resonance. These biological and conformational data are discussed in relation to those of the prototype tripeptide and its methyl ester.
Original languageEnglish
Pages (from-to)66-71
JournalPeptide research
Volume4
Issue number2
Publication statusPublished - 1991

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