Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5407263 | Journal of Magnetic Resonance | 2008 | 6 Pages |
Abstract
17O chemical shifts of Ala-Ala-Ala, with parallel and anti-parallel β-sheet structures, are observed using a 930-MHz high-resolution solid-state NMR spectrometer. Ala-Ala-Ala serves as a model sheet-forming peptide because it can be easily prepared as either a parallel or an anti-parallel β-sheet structure. Spectral differences between the two samples are observed which arise from molecular packing differences between the two sheet structures. DFT chemical shift calculations are performed for the two samples, and the calculated spectra are in good agreement with the experimental spectra. The DFT calculations provide insight into the nature of the chemical shift differences observed between the two sheet structures.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Physical and Theoretical Chemistry
Authors
Kazuo Yamauchi, Michi Okonogi, Hiromichi Kurosu, Masataka Tansho, Tadashi Shimizu, Terry Gullion, Tetsuo Asakura,