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Solvent independent conformational propensities of [1,2,3]triazolyl‐bridged parathyroid hormone‐related peptide‐derived cyclo‐nonapeptide analogues
Author(s) -
Scrima Mario,
Grimaldi Manuela,
Di Marino Sara,
Testa Chiara,
Rovero Paolo,
Papini Anna Maria,
Chorev Michael,
D'Ursi Anna Maria
Publication year - 2012
Publication title -
peptide science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.556
H-Index - 125
eISSN - 1097-0282
pISSN - 0006-3525
DOI - 10.1002/bip.22139
Subject(s) - chemistry , moiety , stereochemistry , peptide , salt bridge , cycloaddition , click chemistry , methylene bridge , isostere , side chain , cyclic peptide , combinatorial chemistry , organic chemistry , biochemistry , catalysis , polymer , mutant , gene
The recently introduced Cu(I)‐catalyzed azide–alkyne 1,3‐dipolar Huisgen cycloaddition as a prototypic “click chemistry reaction” presented an opportunity for introducing the 1,4‐disubstituted‐[1,2,3]triazolyl moiety as a new isostere for peptide bonds in the backbone. Previous study in our lab focused on the synthesis of a model i‐to‐i+4 side chain‐to‐side chain 1,4‐ and 4,1‐disubstituted‐[1,2,3]triazolyl‐bridged cyclo‐nonapeptide I (Scheme 1) as analogues of its structurally related helical i‐to‐i+4 lactam‐bridged cyclo‐nonapeptide [Lys 13 (& 1 ),Asp 17 (& 2 )]parathyroid hormone related peptide (PTHrP)(11–19)NH 2 1 a truncated version of the α‐helical and potent parathyroid hormone receptor 1 agonist [Lys 13 (& 1 ),Asp 17 (& 2 )]PTHrP(1‐34)NH 2 , 2,3 N α ‐Ac‐Lys‐Gly‐Lys(& 1 )‐Ser‐Ile‐Gln‐Asp(& 2 )‐Leu‐Arg‐NH 2 ]. Systematic [1,2,3]triazolyl‐containing bridge structure–conformation relationship studies in hexafluoroacetone/water mixture included incorporation of bridges varied in size and position and orientation of the triazolyl ring within the bridge. These studies revealed that the size of methylene bridge flanking triazolyl moiety is critical to reproduce in the heterodetic cyclo‐nonapeptides. The conformational features of the analogues cyclo‐nonapeptide in which Lys 13 and Asp 17 are bridged by the isosteric lactam. Here, we extend our conformational analysis to dimethyl sulfoxide/water mixture in an effort to characterize inherent conformational properties of the heterodetic cyclopeptides that are solvent independent. Our present study shows that the physicochemical properties of the structure‐supporting solvent cannot override the effect of the size of methylene bridge to form helical mimetic structures. Moreover, we prove that [1,2,3]triazolyl ring is not a simple bioisostere of lactam bond, but it affects the secondary structure of the peptide, in relation to its positioning orientation. © 2012 Wiley Periodicals, Inc. Biopolymers (Pept Sci) 98: 535–545, 2012.