A set of terminally protected tripeptoids containing a residue of either N-methylglycine or N-isobutylglycine in position i+l/i+2 were synthesized and tested for intramolecularly H-bonded beta-turn formation. By exploiting FT-IR absorption and 1H-NMR techniques, their folding tendencies were compared with those of a variety of reference peptides. The amount of beta-turn induction and the relative extent of the various types of intramolecularly H-bonded beta-turn conformers were determined in chloroform solution.
Peptoid residues and beta-turn formation.
CAVICCHIONI, Giorgio
2002
Abstract
A set of terminally protected tripeptoids containing a residue of either N-methylglycine or N-isobutylglycine in position i+l/i+2 were synthesized and tested for intramolecularly H-bonded beta-turn formation. By exploiting FT-IR absorption and 1H-NMR techniques, their folding tendencies were compared with those of a variety of reference peptides. The amount of beta-turn induction and the relative extent of the various types of intramolecularly H-bonded beta-turn conformers were determined in chloroform solution.File in questo prodotto:
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