Two water-soluble 3(10)-helical peptides are synthesized and fully characterized for the first time. The sequence of these terminally blocked heptamers comprises two residues of the C-alpha-trisubstituted alpha -amino acid 2-amino-3-[1-(1,4,7-triazacyclononyl)]propanoic acid and five residues of a C-alpha-tetrasubstituted alpha -amino acid (either alpha -aminoisobutyric acid or isovaline). Using CD and NMR techniques we were able to show that both heptapeptides are well structured in water, and that the type of conformation adopted is indeed the ternary 3(10)-helix.

The First Water-Soluble 310-Helical Peptides

FORMAGGIO, FERNANDO;SCRIMIN, PAOLO MARIA;TONIOLO, CLAUDIO
2000

Abstract

Two water-soluble 3(10)-helical peptides are synthesized and fully characterized for the first time. The sequence of these terminally blocked heptamers comprises two residues of the C-alpha-trisubstituted alpha -amino acid 2-amino-3-[1-(1,4,7-triazacyclononyl)]propanoic acid and five residues of a C-alpha-tetrasubstituted alpha -amino acid (either alpha -aminoisobutyric acid or isovaline). Using CD and NMR techniques we were able to show that both heptapeptides are well structured in water, and that the type of conformation adopted is indeed the ternary 3(10)-helix.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11577/2472469
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