A solid state NMR method is presented for determination of a backbone dihedral angle phi in peptides, being based on the previously reported method, relayed anisotropy correlation (RACO) NMR [Y. Ishii et al., Chem. Phys. Lett. 256 (1996) 133]. In the present method, the 15N-1H and the 13C-1H dipolar
Relayed anisotropy correlation NMR: determination of dihedral angles in solids
β Scribed by Yoshitaka Ishii; Takehiko Terao; Masatsune Kainosho
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 558 KB
- Volume
- 256
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
A two-dimensional solid-state NMR method is proposed for determining the mutual orientation of the two interaction tensors in each of which a different chemical group participates, from which information on the dihedral angle can be extracted. The two-dimensional powder pattern was observed for 1,2-13C-labeled DL-alanine as a demonstration, correlating the L3C 1 chemical shift anisotropy and the L3C 2-I H dipolar coupling via polarization transfer. The O-C 1-C2-H dihedral angle as well as the orientation of the t3C 1 chemical shift tensor were determined from the spectrum.
π SIMILAR VOLUMES
A solid state NMR technique for the determination of peptide backbone conformations at specific sites in unoriented samples under magic angle spinning (MAS) is described and demonstrated on a doubly labeled polycrystalline sample of the tripeptide AlaGlyGly and a sextuply labeled lyophilized sample
## Abstract The principal components and orientations of the chemical shift anisotropy (CSA) tensors of nearly all ^13^C carbonyl nuclei in a small protein have been determined in isotropic solution by a combination of three complementary crossβcorrelation measurements.
Several existing methods permit measurement of the torsion angles Ο, Ο and Ο in peptides and proteins with solid-state MAS NMR experiments. Currently, however, there is not an approach that is applicable to measurement of Ο in the angular range -20 β’ to -70 β’ , commonly found in Ξ±-helical structures
## Abstract Powder patterns and sideband patterns have different strengths when it comes to using them to determine chemical shift parameters. Here, we show that chemical shift parameters can be determined with high accuracy by analysing the correlation pattern from a 2D experiment which correlates