Spectral density mapping at multiple magnetic fields suitable for (13)C NMR relaxation studies
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
27003380
DOI
10.1016/j.jmr.2016.02.016
PII: S1090-7807(16)00119-1
Knihovny.cz E-zdroje
- Klíčová slova
- Carbohydrates, Magnetic field, Nuclear magnetic resonance, Nucleic acids, Relaxation, Spectral density function,
- MeSH
- algoritmy * MeSH
- interpretace statistických dat * MeSH
- magnetická rezonanční spektroskopie s uhlíkem 13C metody MeSH
- magnetické pole MeSH
- malá interferující RNA analýza chemie MeSH
- počítačové zpracování signálu * MeSH
- reprodukovatelnost výsledků MeSH
- senzitivita a specificita MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- malá interferující RNA MeSH
Standard spectral density mapping protocols, well suited for the analysis of (15)N relaxation rates, introduce significant systematic errors when applied to (13)C relaxation data, especially if the dynamics is dominated by motions with short correlation times (small molecules, dynamic residues of macromolecules). A possibility to improve the accuracy by employing cross-correlated relaxation rates and on measurements taken at several magnetic fields has been examined. A suite of protocols for analyzing such data has been developed and their performance tested. Applicability of the proposed protocols is documented in two case studies, spectral density mapping of a uniformly labeled RNA hairpin and of a selectively labeled disaccharide exhibiting highly anisotropic tumbling. Combination of auto- and cross-correlated relaxation data acquired at three magnetic fields was applied in the former case in order to separate effects of fast motions and conformational or chemical exchange. An approach using auto-correlated relaxation rates acquired at five magnetic fields, applicable to anisotropically moving molecules, was used in the latter case. The results were compared with a more advanced analysis of data obtained by interpolation of auto-correlated relaxation rates measured at seven magnetic fields, and with the spectral density mapping of cross-correlated relaxation rates. The results showed that sufficiently accurate values of auto- and cross-correlated spectral density functions at zero and (13)C frequencies can be obtained from data acquired at three magnetic fields for uniformly (13)C-labeled molecules with a moderate anisotropy of the rotational diffusion tensor. Analysis of auto-correlated relaxation rates at five magnetic fields represents an alternative for molecules undergoing highly anisotropic motions.
Central European Institute of Technology Masaryk University Kamenice 5 CZ 625 00 Brno Czech Republic
Department of Organic Chemistry Arrhenius Laboratory Stockholm University S 106 91 Stockholm Sweden
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