Abstract
Urea at ~12 M in concentrated gelatin gel, that was stretched, gave (1)H and (2)H NMR spectral splitting patterns that varied in a predictable way with changes in the relative proportions of (1)H2O and (2)H2O in the medium. This required consideration of the combinatorics of the two amide groups in urea that have a total of four protonation/deuteration sites giving rise to 16 different isotopologues, if all the atoms were separately identifiable. The rate constant that characterized the exchange of the protons with water was estimated by back-transformation analysis of 2D-EXSY spectra. There was no (1)H NMR spectral evidence that the chiral gelatin medium had caused in-equivalence in the protons bonded to each amide nitrogen atom. The spectral splitting patterns in (1)H and (2)H NMR spectra were accounted for by intra-molecular scalar and dipolar interactions, and quadrupolar interactions with the electric field gradients of the gelatin matrix, respectively.
[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.
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nmrlearner
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08-31-2015 09:39 PM
G4-Quartet·M+ Borate Hydrogels
G4-Quartet·M+ Borate Hydrogels
Gretchen Marie Peters, Luke P. Skala, Taylor N. Plank, Hyuntaek Oh, G. N. Manjunatha Reddy, Andrew Marsh, Steven P. Brown, Srinivasa R. Raghavan and Jeffery T. Davis
http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/jacsat/0/jacsat.ahead-of-print/jacs.5b02753/20150421/images/medium/ja-2015-027536_0012.gif
Journal of the American Chemical Society
DOI: 10.1021/jacs.5b02753
http://feeds.feedburner.com/~ff/acs/jacsat?d=yIl2AUoC8zA
http://feeds.feedburner.com/~r/acs/jacsat/~4/Uq1NMrHor9A
nmrlearner
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04-22-2015 12:40 AM
Long-lived spin state of a tripeptide in stretched hydrogel
Long-lived spin state of a tripeptide in stretched hydrogel
Abstract
The longitudinal (T 1), transverse (T 2), and singlet state (T s) relaxation times of the geminal backbone protons (CH2) of l-Leu-Gly-Gly were studied by NMR spectroscopy at 9.4 T in a bovine hide gelatin gel composed in D2O at 25Â*°C. Gelatin granules were dissolved in a hot solution of the tripeptide and then the solution was allowed to gel inside a flexible silicone tubing. With increases in gelatin content, the T...
NMR Detection of pH-Dependent Histidine–Water Proton Exchange Reveals the Conduction Mechanism of a Transmembrane Proton Channel
NMR Detection of pH-Dependent Histidine–Water Proton Exchange Reveals the Conduction Mechanism of a Transmembrane Proton Channel
Fanghao Hu, Klaus Schmidt-Rohr and Mei Hong
http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/jacsat/0/jacsat.ahead-of-print/ja2081185/aop/images/medium/ja-2011-081185_0008.gif
Journal of the American Chemical Society
DOI: 10.1021/ja2081185
http://feeds.feedburner.com/~ff/acs/jacsat?d=yIl2AUoC8zA
http://feeds.feedburner.com/~r/acs/jacsat/~4/C3pPoB5_PR8