The structural preferences of peptides (and depsipeptides) from the achiral MeAib and Hib residues, and the chiral Iva, (alphaMe)Val, (alphaMe)Leu, and (alphaMe)Phe residues, as determined by conformational energy computations, x-ray diffraction analyses, and H-1-nmr and spectroscopic studies, are reviewed and compared with literature data on Aib-containing peptides. The results obtained indicate that helical structures are preferentially adopted by peptides rich in these alpha-amino acids methylated at the alpha-carbon. Intriguing experimental findings on the impact of the chirality of Iva, (alphaMe) Val, and (alphaMe) Phe residues on helix screw sense are illustrated.
Linear Oligopeptide .279. Structures of Peptides From Alpha-amino-acids Methylated At the Alpha-carbon
TONIOLO, CLAUDIO;FORMAGGIO, FERNANDO;
1993
Abstract
The structural preferences of peptides (and depsipeptides) from the achiral MeAib and Hib residues, and the chiral Iva, (alphaMe)Val, (alphaMe)Leu, and (alphaMe)Phe residues, as determined by conformational energy computations, x-ray diffraction analyses, and H-1-nmr and spectroscopic studies, are reviewed and compared with literature data on Aib-containing peptides. The results obtained indicate that helical structures are preferentially adopted by peptides rich in these alpha-amino acids methylated at the alpha-carbon. Intriguing experimental findings on the impact of the chirality of Iva, (alphaMe) Val, and (alphaMe) Phe residues on helix screw sense are illustrated.Pubblicazioni consigliate
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