We have a case of a molecule that has two slowly exchanging conformations. In the NOESY experiment we see cross-relaxing cross-peaks (negative or the opposite sign to the diagonal) for interproton distances as well as exchanging cross-peaks (positive or the same sign as the diagonal). This is the classical expected behavior in such a sample. But...
In this molecule there is a pair of geminal protons for which the phenomenon is exactly reversed: The interproton cross-peak is POSITIVE and the exchange peaks are NEGATIVE. There is no doubt which peak is which (from the COSY, for instance).
I suspect a scrambling effect due to the combined mechanisms, but I hope to be reassured by a clear explanation or comments saying that this has been seen and described before.
Check if somebody has answered this question on NMRWiki QA forum
Did you find this post helpful? |
Similar Threads
Thread
Thread Starter
Forum
Replies
Last Post
Dynamic UltraFast 2D EXchange SpectroscopY (UF-EXSY) of hyperpolarized substrates
From The DNP-NMR Blog:
Dynamic UltraFast 2D EXchange SpectroscopY (UF-EXSY) of hyperpolarized substrates
Leon Swisher, C., et al., Dynamic UltraFast 2D EXchange SpectroscopY (UF-EXSY) of hyperpolarized substrates. J Magn Reson, 2015. 257: p. 102-9.
http://www.ncbi.nlm.nih.gov/pubmed/26117655
nmrlearner
News from NMR blogs
0
09-10-2015 01:10 AM
[Question from NMRWiki Q&A forum] Splitting of amide peaks in indirect proton dimension of a 3D 15N Noesy spectra
Splitting of amide peaks in indirect proton dimension of a 3D 15N Noesy spectra
Hello, I am trying to record 3D 15N Noesy-hsqc experiment on 15N labelled protein (50 a.a). The mixing time is 120 ms and the decoupler for 15N dimension is garp. Only the peaks in the amide region on the indirect proton dimension splitted into doublet with splitting ranging from 76-95 Hz. The 15N_HSQC spectra looks fine. What could be the possible reason for this? Please let me know your thoughts and inputs.
Check if somebody has answered this question on NMRWiki QA forum
nmrlearner
News from other NMR forums
0
08-31-2015 09:39 PM
Reversed-Phase LC Isolates Potent Insecticidal Protein From Tarantula - LCGC Chromatography Online
Reversed-Phase LC Isolates Potent Insecticidal Protein From Tarantula - LCGC Chromatography Online
http://www.bionmr.com//t3.gstatic.com/images?q=tbn:ANd9GcQPvzVNyrq21tcZWrk-F8daI_eTIZQf2JRjrGMp_N-ih8CFKL5y4R-wnmulIW0Ic3xWjeUk_Lq5
LCGC Chromatography Online
<img alt="" height="1" width="1" />
Reversed-Phase LC Isolates Potent Insecticidal Protein From Tarantula
LCGC Chromatography Online
The structure of the peptide, was determined by nuclear magnetic resonance (NMR) spectroscopy and indicated high thermal and chemical stability. According to the paper, this suggests the potential to...
nmrlearner
Online News
0
10-03-2013 03:31 PM
[NMR Sparky Yahoo group] Re: 2d noesy peaks integartion error linefit faileld to converge
Re: 2d noesy peaks integartion error linefit faileld to converge
Hi Srinivas ... this is normally ok, unless you use an exponential window. ... this should be YES in almost all cases I can think of. if it fails to converge
More...
nmrlearner
News from other NMR forums
0
02-07-2012 05:09 PM
[NMR Sparky Yahoo group] 2d noesy peaks integartion error linefit faileld to converge
2d noesy peaks integartion error linefit faileld to converge
Hello sparky users , I am using 2D noesy spectrum (H,H) to do structure calculation , while doing peak integration it is showing errors as follows . Linefit
More...
nmrlearner
News from other NMR forums
0
02-07-2012 04:14 AM
[NMR paper] Suppression of diagonal peaks in TROSY-type 1H NMR NOESY spectra of 15N-labeled prote
Suppression of diagonal peaks in TROSY-type 1H NMR NOESY spectra of 15N-labeled proteins.
Related Articles Suppression of diagonal peaks in TROSY-type 1H NMR NOESY spectra of 15N-labeled proteins.
J Magn Reson. 1999 Oct;140(2):499-503
Authors: Meissner A, Sørensen OW
A novel method for suppression of diagonal peaks in the amide region of NOESY NMR spectra of 15N-labeled proteins is presented. The method is particularly useful for larger proteins at high magnetic fields where interference between dipolar and chemical shift anisotropy relaxation...