Simultaneous cross polarization to (13)C and (15)N with (1)H detection at 60kHz MAS solid-state NMR

J Magn Reson. 2016 Jan:262:20-26. doi: 10.1016/j.jmr.2015.12.004. Epub 2015 Dec 12.

Abstract

We describe high resolution MAS solid-state NMR experiments that utilize (1)H detection with 60kHz magic angle spinning; simultaneous cross-polarization from (1)H to (15)N and (13)C nuclei; bidirectional cross-polarization between (13)C and (15)N nuclei; detection of both amide nitrogen and aliphatic carbon (1)H; and measurement of both (13)C and (15)N chemical shifts through multi-dimensional correlation experiments. Three-dimensional experiments correlate amide (1)H and alpha (1)H selectively with (13)C or (15)N nuclei in a polypeptide chain. Two separate three-dimensional spectra correlating (1)Hα/(13)Cα/(1)H(N) and (1)H(N)/(15)N/(1)Hα are recorded simultaneously in a single experiment, demonstrating that a twofold savings in experimental time is potentially achievable. Spectral editing using bidirectional coherence transfer pathways enables simultaneous magnetization transfers between (15)N, (13)Cα(()(i)()) and (13)C'(()(i)(-1)), facilitating intra- and inter-residue correlations for sequential resonance assignment. Non-uniform sampling is integrated into the experiments, further reducing the length of experimental time.

Keywords: Dual observation; Magic angle spinning; Peptides; Proteins; Triple-resonance.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Amides / chemistry
  • Bacteriophage M13 / chemistry
  • Capsid Proteins / chemistry
  • Carbon Isotopes
  • Nitrogen Isotopes
  • Nuclear Magnetic Resonance, Biomolecular / methods*
  • Oligopeptides / chemistry
  • Peptides / chemistry
  • Proteins / chemistry
  • Protons

Substances

  • Amides
  • Capsid Proteins
  • Carbon Isotopes
  • Nitrogen Isotopes
  • Oligopeptides
  • Peptides
  • Proteins
  • Protons