Determination of internal dynamics of deoxyriboses in the DNA hexamer d(CGTACG)2 by 1H NMR

1989 ◽  
Vol 17 (4) ◽  
Author(s):  
A.N. Lane ◽  
M.J. Forster
Keyword(s):  
1H Nmr ◽  
1978 ◽  
Vol 43 (10) ◽  
pp. 2609-2618 ◽  
Author(s):  
Bruno Schönecker ◽  
Dieter Tresselt ◽  
Gerd Schubert ◽  
Ladislav Kohout ◽  
Jan Fajkoš

2021 ◽  
Vol 75 (2-3) ◽  
pp. 119-131
Author(s):  
Albert A. Smith ◽  
Nicolas Bolik-Coulon ◽  
Matthias Ernst ◽  
Beat H. Meier ◽  
Fabien Ferrage

AbstractThe dynamics of molecules in solution is usually quantified by the determination of timescale-specific amplitudes of motions. High-resolution nuclear magnetic resonance (NMR) relaxometry experiments—where the sample is transferred to low fields for longitudinal (T1) relaxation, and back to high field for detection with residue-specific resolution—seeks to increase the ability to distinguish the contributions from motion on timescales slower than a few nanoseconds. However, tumbling of a molecule in solution masks some of these motions. Therefore, we investigate to what extent relaxometry improves timescale resolution, using the “detector” analysis of dynamics. Here, we demonstrate improvements in the characterization of internal dynamics of methyl-bearing side chains by carbon-13 relaxometry in the small protein ubiquitin. We show that relaxometry data leads to better information about nanosecond motions as compared to high-field relaxation data only. Our calculations show that gains from relaxometry are greater with increasing correlation time of rotational diffusion.


2005 ◽  
Vol 61 (2) ◽  
pp. 155-161 ◽  
Author(s):  
Eduardo Fernandez-Megia ◽  
Ramón Novoa-Carballal ◽  
Emilio Quiñoá ◽  
Ricardo Riguera
Keyword(s):  
1H Nmr ◽  

ChemInform ◽  
2010 ◽  
Vol 23 (40) ◽  
pp. no-no
Author(s):  
D. R. BOYD ◽  
N. D. SHARMA ◽  
R. BOYLE ◽  
R. A. S. MCMORDIE ◽  
J. CHIMA ◽  
...  

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