(PDF) An efficient 3D NMR technique for correlating the proton and 15 N backbone amide resonances with the ??-carbon of the preceding residue in uniformly 15 N/ 13 C enriched proteins - ResearchGate
(PDF) An efficient 3D NMR technique for correlating the proton and 15 N backbone amide resonances with the ??-carbon of the preceding residue in uniformly 15 N/ 13 C enriched proteins - ResearchGate
(PDF) An efficient 3D NMR technique for correlating the proton and 15 N backbone amide resonances with the ??-carbon of the preceding residue in uniformly 15 N/ 13 C enriched proteins - ResearchGate
Creating a clinical platform for carbon-13 studies using the sodium-23 and proton resonances #DNPNMR
From The DNP-NMR Blog:
Creating a clinical platform for carbon-13 studies using the sodium-23 and proton resonances #DNPNMR
Grist, James T., Esben S.S. Hansen, Juan D. Sánchez-Heredia, Mary A. McLean, Rasmus Tougaard, Frank Riemer, Rolf F. Schulte, et al. “Creating a Clinical Platform for Carbon-13 Studies Using the Sodium-23 and Proton Resonances.” Magnetic Resonance in Medicine, March 13, 2020, mrm.28238.
https://doi.org/10.1002/mrm.28238.
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06-11-2020 06:01 PM
Creating a clinical platform for carbon-13 studies using the sodium-23 and proton resonances #DNPNMR
From The DNP-NMR Blog:
Creating a clinical platform for carbon-13 studies using the sodium-23 and proton resonances #DNPNMR
Grist, James T., Esben S.S. Hansen, Juan D. Sánchez-Heredia, Mary A. McLean, Rasmus Tougaard, Frank Riemer, Rolf F. Schulte, et al. “Creating a Clinical Platform for Carbon-13 Studies Using the Sodium-23 and Proton Resonances.” Magnetic Resonance in Medicine, March 13, 2020, mrm.28238.
https://doi.org/10.1002/mrm.28238.
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06-03-2020 11:09 PM
Sensitivity-enhanced detection of non-labile proton and carbon NMR spectra on water resonances #DNPNMR
From The DNP-NMR Blog:
Sensitivity-enhanced detection of non-labile proton and carbon NMR spectra on water resonances #DNPNMR
Novakovic, M., et al., Sensitivity-enhanced detection of non-labile proton and carbon NMR spectra on water resonances. Phys. Chem. Chem. Phys., 2017. 20(1): p. 56-62.
https://www.ncbi.nlm.nih.gov/pubmed/29171604
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02-19-2018 08:46 PM
[NMR paper] (13)C (?) decoupling during direct observation of carbonyl resonances in solution NMR of isotopically enriched proteins.
(13)C (?) decoupling during direct observation of carbonyl resonances in solution NMR of isotopically enriched proteins.
Related Articles (13)C (?) decoupling during direct observation of carbonyl resonances in solution NMR of isotopically enriched proteins.
J Biomol NMR. 2014 Aug 17;
Authors: Ying J, Li F, Lee JH, Bax A
Abstract
Direct detection of (13)C can be advantageous when studying uniformly enriched proteins, in particular for paramagnetic proteins or when hydrogen exchange with solvent is fast. A scheme recently...
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08-19-2014 11:21 AM
13Cα decoupling during direct observation of carbonyl resonances in solution NMR of isotopically enriched proteins
13Cα decoupling during direct observation of carbonyl resonances in solution NMR of isotopically enriched proteins
Abstract
Direct detection of 13C can be advantageous when studying uniformly enriched proteins, in particular for paramagnetic proteins or when hydrogen exchange with solvent is fast. A scheme recently introduced for long-observation-window band-selective homonuclear decoupling in solid state NMR, LOW-BASHD (Struppe et al. in J Magn Reson 236:89â??94, 2013) is shown to be effective for 13Cα decoupling during direct 13Câ?² observation in...
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08-16-2014 10:26 PM
Restraints on backbone conformations in solid state NMR studies of uniformly labeled proteins from quantitative amide 15N–15N and carbonyl 13C–13C dipolar recoupling data
Restraints on backbone conformations in solid state NMR studies of uniformly labeled proteins from quantitative amide 15N–15N and carbonyl 13C–13C dipolar recoupling data
May 2012
Publication year: 2012
Source:Journal of Magnetic Resonance, Volume 218</br>
</br>
Recent structural studies of uniformly 15N, 13C-labeled proteins by solid state nuclear magnetic resonance (NMR) rely principally on two sources of structural restraints: (i) restraints on backbone conformation from isotropic 15N and 13C chemical shifts, based on empirical correlations between chemical shifts and...
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02-03-2013 10:13 AM
Restraints on backbone conformations in solid state NMR studies of uniformly labeled proteins from quantitative amide 15N-15N and carbonyl 13C-13C dipolar recoupling data
Restraints on backbone conformations in solid state NMR studies of uniformly labeled proteins from quantitative amide 15N-15N and carbonyl 13C-13C dipolar recoupling data
Publication year: 2012
Source:Journal of Magnetic Resonance</br>
Kan-Nian Hu, Wei Qiang, Guillermo A. Bermejo, Charles D. Schwieters, Robert Tycko</br>
Recent structural studies of uniformly 15N,13C-labeled proteins by solid state nuclear magnetic resonance (NMR) rely principally on two sources of structural restraints: (i) restraints on backbone conformation from isotropic 15N and 13C chemical...
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03-10-2012 10:54 AM
[NMR paper] An efficient 3D NMR technique for correlating the proton and 15N backbone amide reson
An efficient 3D NMR technique for correlating the proton and 15N backbone amide resonances with the alpha-carbon of the preceding residue in uniformly 15N/13C enriched proteins.
Related Articles An efficient 3D NMR technique for correlating the proton and 15N backbone amide resonances with the alpha-carbon of the preceding residue in uniformly 15N/13C enriched proteins.
J Biomol NMR. 1991 May;1(1):99-104
Authors: Bax A, Ikura M
A 3D NMR technique is described which correlates the amide proton and nitrogen resonances of an amino acid residue...