1H-1H MAS correlation spectroscopy and distance measurements in a deuterated peptide

J Magn Reson. 2001 Aug;151(2):320-7. doi: 10.1006/jmre.2001.2354.

Abstract

In this Communication, we demonstrate the use of deuteration together with back substitution of exchangeable protons as a means of attenuating the strong 1H-1H couplings that broaden 1H magic angle spinning (MAS) spectra of solids. The approach facilitates 15N-1H correlation experiments as well as experiments for the measurement of 1H-1H distances. The distance measurement relies on the excellent resolution in the 1H MAS spectrum and homonuclear double quantum recoupling techniques. The 1H-1H dipolar recoupling can be analyzed in an analytical fashion by fitting the data to a 2- or 3-spin system. The experiments are performed on a sample of the dipeptide N-Ac-Val-Leu-OH, which was synthesized from uniformly [2H, 15N] labeled materials and back-exchanged in H2O.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Deuterium
  • Magnetic Resonance Spectroscopy / methods*
  • Mathematics
  • Molecular Conformation
  • Peptides / chemistry*
  • Signal Processing, Computer-Assisted

Substances

  • Peptides
  • Deuterium