Autor(es): Carvalho, Carina Martins ; Castro, Vânia I. B. ; Costa, Susana P. G. ; Pereira-Lima, Sílvia M. M. A.
Data: 2013
Identificador Persistente: http://hdl.handle.net/1822/37373
Origem: RepositóriUM - Universidade do Minho
Projeto/bolsa: info:eu-repo/grantAgreement/FCT/5876-PPCDTI/118389/PT ; info:eu-repo/grantAgreement/FCT/COMPETE/118389/PT;
Assunto(s): Peptaibolin; Conformational studies; Ciências Naturais::Ciências Químicas
Comunicação em painel PC139.
We report the conformational studies on a model peptide, Peptaibolin (Ac-Leu-Aib-Leu-Aib-Phol) and its mimetics incorporating unnatural α,α-dialkylglycines bearing longer and bulkier side chains in order to gain insight about the conformational preferences resulting from substitution of the native Aib residues. An Ala analogue was studied as a control in the conformational study. The influence imposed by the bulkier and more hydrophobic amino acids in the peptide chain was evaluated through IR spectroscopy and 1D and 2D NMR techniques, revealing certain conformational preferences.
