Publication date: Available online 4 December 2014 Source:Journal of Magnetic Resonance
Author(s): Kang Chen , Darón I. Freedberg , David A. Keire
2D NMR 1H-X (X=15N or 13C) HSQC spectra contain cross-peaks for all XHn moieties. Multiplicity-edited 1H-13C HSQC pulse sequences generate opposite signs between peaks of CH2 and CH/CH3 at a cost of lower signal-to-noise due to the 13C T2 relaxation during an additional 1/1 J CH period. Such CHn-editing experiments are useful in assignment of chemical shifts and have been successfully applied to small molecules and small proteins (e.g. ubiquitin) dissolved in deuterated solvents where, generally, peak overlap is minimal. By contrast, for larger biomolecules, peak overlap in 2D HSQC spectra is unavoidable and peaks with opposite phases cancel each other in the edited spectra. However, there is an increasing need for using NMR to profile biomolecules at natural abundance dissolved in water (e.g., protein therapeutics) where NMR experiments beyond 2D are impractical. Therefore, the existing 2D multiplicity-edited HSQC methods must be improved to acquire data on nuclei other than 13C (i.e. 15N), to resolve more peaks, to reduce T2 losses and to accommodate water suppression approaches. To meet these needs, a multiplicity-separated 1H-X HSQC (MS-HSQC) experiment was developed and tested on 500 and 700 MHz NMR spectrometers equipped with a room temperature probe using RNase A (14 kDa) and retroviral capsid (26 kDa) proteins dissolved in 95%H2O/5%D2O. In this pulse sequence, the 1/1 J XH editing-period is incorporated into the semi-constant time (semi-CT) X resonance chemical shift evolution period, which increases sensitivity, and importantly, the sum and the difference of the interleaved 1 J XH-active and the 1 J XH-inactive HSQC experiments yield two separate spectra for XH2 and XH/XH3. Furthermore we demonstrate improved water suppression using triple xyz-gradients instead of the more widely used z-gradient only water-suppression approach. Graphical abstract
Measuring long-lived (13)C2 state lifetimes at natural abundance
From The DNP-NMR Blog:
Measuring long-lived (13)C2 state lifetimes at natural abundance
Claytor, K., et al., Measuring long-lived (13)C2 state lifetimes at natural abundance. J Magn Reson, 2014. 239(0): p. 81-6.
http://www.ncbi.nlm.nih.gov/pubmed/24457544
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Rapid Heteronuclear Single Quantum Correlation NMR Spectra at Natural Abundance
Rapid Heteronuclear Single Quantum Correlation NMR Spectra at Natural Abundance
David Schulze-Su?nninghausen, Johanna Becker and Burkhard Luy
http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/jacsat/0/jacsat.ahead-of-print/ja411588d/aop/images/medium/ja-2013-11588d_0005.gif
Journal of the American Chemical Society
DOI: 10.1021/ja411588d
http://feeds.feedburner.com/~ff/acs/jacsat?d=yIl2AUoC8zA
http://feeds.feedburner.com/~r/acs/jacsat/~4/TExWpxpxjak
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Dynamic Nuclear Polarization Enhanced Natural Abundance 17O Spectroscopy
From the The DNP-NMR Blog:
Dynamic Nuclear Polarization Enhanced Natural Abundance 17O Spectroscopy
Blanc, F., et al., Dynamic Nuclear Polarization Enhanced Natural Abundance 17O Spectroscopy. J. Am. Chem. Soc., 2013. 135(8): p. 2975-2978.
http://dx.doi.org/10.1021/ja4004377
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More AccurateJCHCoupling Measurement in the Presence ofJHHStrong Coupling in Natural Abundance
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Publication year: 2011
Source: Journal of Magnetic Resonance, Available online 22 September 2011</br>
Bingwu*Yu, Hugo*van Ingen, Subramanian*Vivekanandan, Christoph*Rademacher, Scott E.*Norris, ...</br>
Jcouplings are essential for measuring RDCs (residual dipolar couplings), now routinely used to deduce molecular structure and dynamics of glycans and proteins. Accurate measurement ofJCHis critical for RDCs to reflect the true structure and dynamics in the molecule of interest. We report...
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