Accurate determination of order parameters fromH,N dipolar couplings in MAS solid-state NMR experiments
Journal of the American Chemical Society, ISSN: 0002-7863, Vol: 131, Issue: 39, Page: 14018-14022
2009
- 89Citations
- 80Captures
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Metrics Details
- Citations89
- Citation Indexes89
- 89
- CrossRef86
- Captures80
- Readers80
- 80
Article Description
A reliable site-specific estimate of the individual N-H bond lengths in the protein backbone is the fundamental basis of any relaxation experiment in solution and in the solid-state NMR. The N-H bond length can in principle be influenced by hydrogen bonding, which would result in an increased N-H distance. At the same time, dynamics in the backbone induces a reduction of the experimental dipolar coupling due to motional averaging. We present a 3D dipolar recoupling experiment in which the H,N dipolar coupling is reintroduced in the indirect dimension using phase-inverted CP to eliminate effects from rf inhomogeneity. We find no variation of the N-H dipolar coupling as a function of hydrogen bonding. Instead, variations in the H,N dipolar coupling seem to be due to dynamics of the protein backbone. This is supported by the observed correlation between the H-N dipolar coupling and the amide proton chemical shift. The experiment is demonstrated for a perdeuterated sample of the α-spectrin SH3 domain. Perdeuteration is a prerequisite to achieve high accuracy. The average error in the analysis of the H-N dipolar couplings is on the order of ±370 Hz (±0.012 Å) and can be as small as 150 Hz, corresponding to a variation of the bond length of ±0.005 Å. © 2009 American Chemical Society.
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