Parallel acquisition NMR spectroscopy (PANSY) is used to detect simultaneously signals from up to four nuclear species, such as H-1, H-2, C-13, N-15, F-19 and P-31. The conventional COSY, TOCSY, HSQC, HMQC and HMBC pulse sequences have been adapted for such applications. Routine availability of NMR systems that incorporate multiple receivers has led to development of new types of NMR experiments. One such scheme named PANACEA allows unambiguous structure determination of small organic molecules from a single measurement and includes an internal field/frequency correction routine. It does not require the conventional NMR lock system and can be recorded in pure liquids. Furthermore, long-range spin-spin couplings can be extracted from the PANACEA spectra and used for three-dimensional structure refinement. In bio-molecular NMR, multi-receiver NMR systems are used for simultaneous recording of H-1 and C-13 detected multi-dimensional spectra. For instance, the 2D (HA)CACO and 3D (HA)CA(CO)NNH experiments can be recorded simultaneously in proteins of moderate size (up to 30*kDa). The multi-receiver experiments can also be used in combination with the fast acquisition schemes such as Hadamard spectroscopy, computer optimized aliasing and projection-reconstruction techniques. In general, experiments that utilize multiple receivers provide significantly more information from a single NMR measurement as compared to the conventional single receiver techniques.
PMID: 21837554 [PubMed - as supplied by publisher]
Simultaneous acquisition of 13Cαâ??15N and 1Hâ??15Nâ??15N sequential correlations in proteins: application of dual receivers in 3D HNN
Simultaneous acquisition of 13Cαâ??15N and 1Hâ??15Nâ??15N sequential correlations in proteins: application of dual receivers in 3D HNN
Abstract We describe here, adaptation of the HNN pulse sequence for multiple nuclei detection using two independent receivers by utilizing the detectable 13Cα transverse magnetization which was otherwise dephased out in the conventional HNN experiment. It enables acquisition of 2D 13Cαâ??15N sequential correlations along with the standard 3D 15Nâ??15Nâ??1H correlations, which provides directionality to sequential walk in HNN, on one hand, and enhances...
[NMRpipe Yahoo group] Re: Propagating resonance positions to multiple spectra
Re: Propagating resonance positions to multiple spectra
If you are building individual peak tables for each plane of a 2D relaxation series, there's probably a better way to do the analysis. Have a look at the
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08-23-2011 05:31 PM
[NMRpipe Yahoo group] Propagating resonance positions to multiple spectra
Propagating resonance positions to multiple spectra
Hello, Is it possible in NMRPipe to: 1. Generate a peak table for a new spectrum using the resonance positions in an existing peak table? 2. Update the peak
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08-22-2011 05:26 PM
Detecting the "Afterglow" of (13)C NMR in Proteins Using Multiple Receivers.
Detecting the "Afterglow" of (13)C NMR in Proteins Using Multiple Receivers.
Related Articles Detecting the "Afterglow" of (13)C NMR in Proteins Using Multiple Receivers.
J Am Chem Soc. 2010 Dec 2;
Authors: Kupc?e E, Kay LE, Freeman R
We show that the weak signal that remains after (13)C-detected experiments (the (13)C "afterglow") can still be measured with high sensitivity by proton detection. This is illustrated by the incorporation of two experiments, 2D (HA)CACO and 3D (HA)CA(CO)NNH, into a single pulse sequence that makes use of two receivers...
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12-04-2010 07:24 PM
Detecting the “Afterglow” of 13C NMR in Proteins Using Multiple Receivers
Detecting the “Afterglow” of 13C NMR in Proteins Using Multiple Receivers
E?riks Kupc?e, Lewis E. Kay and Ray Freeman
http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/jacsat/0/jacsat.ahead-of-print/ja1080025/aop/images/medium/ja-2010-080025_0002.gif
Journal of the American Chemical Society
DOI: 10.1021/ja1080025
http://feeds.feedburner.com/~ff/acs/jacsat?d=yIl2AUoC8zA
http://feeds.feedburner.com/~r/acs/jacsat/~4/YNH74d-9ntc