J-modulated TROSY experiment extends the limits of homonuclear coupling measurements for larger proteins

J Magn Reson. 2001 Jul;151(1):60-4. doi: 10.1006/jmre.2001.2344.

Abstract

This paper describes the use of a TROSY experimental scheme and its variant extended with a scaled J-modulation spin-echo sequence for accurate and sensitive measurement of homonuclear 3J(H(N)H(alpha)) coupling constants in larger proteins with uniform 15N labeling. Exclusive selection of the most slowly relaxing component of a 15N-1H multiplet by the TROSY approach leads to substantial improvement in resolution; this is a prerequisite for accurate measurement of couplings from the 1H multiplets directly along the 1H frequency dimension or from the J-scaled doublets along the 15N frequency dimension.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Algorithms
  • Magnetic Resonance Spectroscopy
  • Nitrogen Isotopes
  • Proteins / chemistry*
  • Ribonucleases / chemistry
  • Ubiquitins / chemistry

Substances

  • Nitrogen Isotopes
  • Proteins
  • Ubiquitins
  • Ribonucleases