Publication | Closed Access
High Resolution <sup>1</sup>H Detected <sup>1</sup>H,<sup>13</sup>C Correlation Spectra in MAS Solid-State NMR using Deuterated Proteins with Selective <sup>1</sup>H,<sup>2</sup>H Isotopic Labeling of Methyl Groups
116
Citations
13
References
2006
Year
Magnetic ResonanceMolecular BiologyBiological SolidsMethyl GroupsSolution-state Nmr ExperimentsMas Solid-state NmrDeuterated ProteinsDeuteration SchemeBiophysicsBiochemistrySolution Nmr SpectroscopyStructural BiologyMagnetic Resonance SpectroscopyNatural SciencesSpectroscopyResonanceMass SpectrometryDynamic Nuclear PolarizationProtein NmrMedicineNuclear Magnetic Resonance Spectroscopy
MAS solid-state NMR experiments applied to biological solids are still hampered by low sensitivity and resolution. In this work, we employ a deuteration scheme in which individual methyl groups are selectively protonated. This labeling scheme allows the acquisition of proton carbon correlation spectra with a resolution comparable to that in solution-state NMR experiments. We observe an increase in resolution by a factor of 10-15 compared to standard heteronuclear correlation experiments using PMLG for 1H,1H dipolar decoupling in the indirect dimension. At the same time, the full sensitivity of the proton-based experiment is retained. In comparison to the heteronuclear detected version of the experiment, a gain in sensitivity of a factor of approximately 4.7 is achieved.
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