ArticleJournal of magnetic resonance (San Diego, Calif. : 1997)2011
Cross-correlations between low-γ nuclei in solids via a common dipolar bath.
Article in Journal of magnetic resonance (San Diego, Calif. : 1997), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- Homonuclear Chemical Shift Correlation in Solids Under MAS by Fast Cross-Relaxation Driven Spin Diffusion.bioRxiv : the preprint server for biology · 2025Article
- 3D ¹⁵N/¹⁵N/¹H chemical shift correlation experiment utilizing an RFDR-based ¹H/¹H mixing period at 100 kHz MAS.Journal of magnetic resonance (San Diego, Calif. : 1997) · 2014Article
- Mechanism of dilute-spin-exchange in solid-state NMR.The Journal of chemical physics · 2014Article
- Sensitivity and resolution enhancement of oriented solid-state NMR: application to membrane proteins.Progress in nuclear magnetic resonance spectroscopy · 2013Review
- Experiments optimized for magic angle spinning and oriented sample solid-state NMR of proteins.The journal of physical chemistry. B · 2013Article
- Identifying inter-residue resonances in crowded 2D (13)C- (13)C chemical shift correlation spectra of membrane proteins by solid-state MAS NMR difference spectroscopy.Journal of biomolecular NMR · 2013Article
- The magic of bicelles lights up membrane protein structure.Chemical reviews · 2012Review
- A spectroscopic assignment technique for membrane proteins reconstituted in magnetically aligned bicelles.Journal of biomolecular NMR · 2012Article
Corrections and comments
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Authors and funding
3 authors.
Funding
Abstract
Correlation of chemical shifts of low-γ nuclei (such as 15N) is an important method for assignment of resonances in uniformly-labeled biological solids. Under static experimental conditions, an efficient mixing of low-γ nuclear spin magnetization can be achieved by a thermal contact to the common reservoir of dipole-dipole interactions in order to create 15N-15N, 13C-13C, or 15N-13C cross-peaks in a 2D correlation spectrum. A thermodynamic approach can be used to understand the mechanism of magnetization mixing in various 2D correlation pulse sequences. This mechanism is suppressed under magic-angle spinning, when mixing via direct cross-polarization with protons becomes more efficient. Experimental results are presented for single-crystalline and powder samples of 15N-labeled N-acetyl-L-15N-valyl-L-15N-leucine (NAVL). In addition to the thermodynamic analysis of mixing pulse sequences, two different new mixing sequences utilizing adiabatic pulses are also experimentally demonstrated.
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