13C CP/MAS and direct single pulse 13C MAS NMR with high power decoupling can give very different results for a wide variety of materials. 13C CP/MAS NMR relies on the transfer of magnetization from protons to 13C via the dipolar coupling mechanism whereas the direct single pulse method does not. An interesting material to demonstrate this principle is the shell of a chicken egg. Chicken eggshell is a complex bio-mineral consisting largely (~ 95%) of the calcite polymorph of calcium carbonate as well as proteins and lipids. The 13C CP/MAS and 13C single pulse MAS NMR spectra of a sample of dry ground eggshell, from which the membranes had been removed, are shown in the lower and upper traces in the figure below, respectively.
The 13C CP/MAS spectrum in the lower trace has very broad resonances in the aliphatic region of the spectrum due to the proteins and lipids. The carbonyl region of the spectrum consists of two resonances; one at ~173 ppm due to the carbonyl carbons of the amino acid residues of the proteins and a resonance at ~169 ppm which has been shown1,2 to originate from bicarbonate ions (HCO3)-. Although ~95% the eggshell consists of CaCO3, the carbonate resonance is not present in the 13C CP/MAS spectrum as there are no proximate protons for cross polarization. In contrast, the single pulse 13C MAS spectrum in the top trace shows only the 13C resonance from the carbonate ions which has a coincident chemical shift with that of the bicarbonate ions. All of the other 13C resonances are buried in the noise as they are in much lower concentration. These spectra are an excellent example of how one can obtain different information from 13C CP/MAS and single pulse 13C MAS spectra.
1. D.M. Pisklak, L. Szcleszczuk, I. Wawer, Journal of Agricultural and Food Chemistry, 60, 12254 (2012).
2. J. Feng, Y.J. Lee, R.J. Reeder, B.L. Phillips, American Mineralogist, 91, 957 (2006).
Thermal stability of chicken brain α-spectrin repeat 17: a spectroscopic study
Thermal stability of chicken brain α-spectrin repeat 17: a spectroscopic study
Abstract Spectrin is a rod-like multi-modular protein that is mainly composed of triple-helical repeats. These repeats show very similar 3D-structures but variable conformational and thermodynamical stabilities, which may be of great importance for the flexibility and dynamic behaviour of spectrin in the cell. For instance, repeat 17 (R17) of the chicken brain spectrin α-chain is four times less stable than neighbouring repeat 16 (R16) in terms of ∆G. The structure of spectrin repeats has mainly been...
Temperature dependence of fast carbonyl backbone dynamics in chicken villin headpiece subdomain
Temperature dependence of fast carbonyl backbone dynamics in chicken villin headpiece subdomain
Abstract Temperature-dependence of protein dynamics can provide information on details of the free energy landscape by probing the characteristics of the potential responsible for the fluctuations. We have investigated the temperature-dependence of picosecond to nanosecond backbone dynamics at carbonyl carbon sites in chicken villin headpiece subdomain protein using a combination of three NMR relaxation rates: 13Câ?² longitudinal rate, and two cross-correlated rates involving dipolar and...
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[NMR paper] Letters to the Editor: NMR assignment of the chicken prion protein fragments chPrP(12
Letters to the Editor: NMR assignment of the chicken prion protein fragments chPrP(128-242) and chPrP(25-242) / NMR assignment of the turtle prion protein fragment tPrP(121-225).
Letters to the Editor: NMR assignment of the chicken prion protein fragments chPrP(128-242) and chPrP(25-242) / NMR assignment of the turtle prion protein fragment tPrP(121-225).
J Biomol NMR. 2004 Sep;30(1):97
Authors:
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[NMR paper] Thallium-205 and carbon-13 NMR studies of human sero- and chicken ovotransferrin.
Thallium-205 and carbon-13 NMR studies of human sero- and chicken ovotransferrin.
Related Articles Thallium-205 and carbon-13 NMR studies of human sero- and chicken ovotransferrin.
Biochemistry. 1994 Mar 22;33(11):3304-11
Authors: Aramini JM, Krygsman PH, Vogel HJ
We have examined the binding of Tl3+ to human serotransferrin and chicken ovotransferrin in the presence of carbonate and oxalate by 205Tl and 13C NMR spectroscopy. With carbonate as the synergistic anion, one observes two 205Tl NMR signals due to the bound metal ion in the two...
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08-22-2010 03:33 AM
[NMR paper] Thallium-205 and carbon-13 NMR studies of human sero- and chicken ovotransferrin.
Thallium-205 and carbon-13 NMR studies of human sero- and chicken ovotransferrin.
Related Articles Thallium-205 and carbon-13 NMR studies of human sero- and chicken ovotransferrin.
Biochemistry. 1994 Mar 22;33(11):3304-11
Authors: Aramini JM, Krygsman PH, Vogel HJ
We have examined the binding of Tl3+ to human serotransferrin and chicken ovotransferrin in the presence of carbonate and oxalate by 205Tl and 13C NMR spectroscopy. With carbonate as the synergistic anion, one observes two 205Tl NMR signals due to the bound metal ion in the two...
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08-22-2010 03:33 AM
[NMR paper] 13C NMR studies of protein motional dynamics in bovine, human, rat, and chicken ocula
13C NMR studies of protein motional dynamics in bovine, human, rat, and chicken ocular lenses.
http://www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--linkinghub.elsevier.com-ihub-images-PubMedLink.gif Related Articles 13C NMR studies of protein motional dynamics in bovine, human, rat, and chicken ocular lenses.
Exp Eye Res. 1993 Mar;56(3):305-16
Authors: Rydzewski JM, Wang SX, Stevens A, Serdahl C, Schleich T
The motional dynamics of lens proteins were studied by two 13C nuclear magnetic resonance (NMR) techniques sensitive to molecular...
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08-21-2010 11:53 PM
[NMR paper] Determination of the secondary structural elements of chicken liver fatty acid bindin
Determination of the secondary structural elements of chicken liver fatty acid binding protein by two-dimensional homonuclear NMR.
http://www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--www3.interscience.wiley.com-aboutus-images-wiley_interscience_pubmed_logo_120x27.gif Related Articles Determination of the secondary structural elements of chicken liver fatty acid binding protein by two-dimensional homonuclear NMR.
Biopolymers. 1999 Jul;50(1):1-11
Authors: Schievano E, Mammi S, Peggion E
A conformational study in solution of the fatty acid...