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Updated: Jul 8, 2026

Structure and Coordination Determination of Peptide-metal Complexes Using 1D and 2D 1H NMR
Published on: December 16, 2013
Determining dihedral angles and local structure in silk peptide by 13C-2H REDOR
Terry Gullion1, Raghuvansh Kishore, Tetsuo Asakura
1Department of Chemistry, West Virginia University, Morgantown, WV 26506, USA. terry.gullion@mail.wvu.edu
Abstract:
13C-2H REDOR NMR experiments were performed on 30-residue (AlaGly)15 silk I mimics of Bombyx mori silk fibroin to gain structural details about the elusive structure of the silk I conformation. 13C,2H-labeling strategies are illustrated for measuring individual dihedral angles in peptides and for determining local structure by REDOR. A major turn of type II character is found in the region Gly(14)-Ala(17).
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