Prasad, Sudhanand and Balaji, Rao R and Bergstrand, Hakan and Lundquist, Britta and Becker, Elmer L and Balaram, P (1996) Conformation-activity correlations for chemotactic tripeptide analogs incorporating dialkyl residues with linear and cyclic alkyl sidechains at position 2. In: International Journal Of Peptide And Protein Research, 48 (04). pp. 312-318.
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Abstract
Five stereochemically constrained analogs of the chemotactic tripeptide incorporating 1-aminocycloalkane-1-carboxylic acid (Ac(n)c) and alpha,alpha-dialkylglycines (Deg, diethylglycine; Dpg, n,n-dipropylglycine and Dbg, n,n-dibutylglycine) at position 2 have been synthesized. NMR studies of peptides For-Met-Xxx-Phe-OMe (Xxx = Ac(7)c, I; Ac(8)c, II; Deg, III; Dpg, IV and Dbg, V; For, formyl) establish that peptides with cycloalkyl residues, I and II, adopt folded beta-turn conformations in CDCl3 and (CD3)(2)SO. In contrast, analogs with linear alkyl sidechains, III-V, favour fully extended (C-5) conformations in solution. Peptides I-V exhibit high activity in inducing beta-glucosaminidase release from rabbit neutrophils, with ED(50) values ranging from 1.4-8.0 x 10(-11)M. In human neutrophils the Dxg peptides III-V have ED(50) values ranging from 2.3 x 10(-8) to 5.9 x 10(-10) M, with the activity order being V > IV > III. While peptides I-IV are less active than the parent. For-Met-Leu-Phe-OH, in stimulating histamine release from human basophils, the Dbg peptide V is appreciably more potent, suggesting its potential utility as a probe for formyl peptide receptors.
Item Type: | Journal Article |
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Publication: | International Journal Of Peptide And Protein Research |
Publisher: | Munksgaard |
Additional Information: | Copyright of this article belongs to Munksgaard. |
Keywords: | chemotactic peptides;alpha,alpha-dialkylated residues; peptide conformation;beta-turns. |
Department/Centre: | Division of Biological Sciences > Molecular Biophysics Unit |
Date Deposited: | 05 Mar 2009 09:02 |
Last Modified: | 25 Feb 2019 08:42 |
URI: | http://eprints.iisc.ac.in/id/eprint/19249 |
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