Selective 1H- 13C NMR spectroscopy of methyl groups in residually protonated samples of large proteins

J Biomol NMR. 2010 Feb;46(2):127-33. doi: 10.1007/s10858-009-9393-0. Epub 2009 Dec 3.

Abstract

Methyl (13)CHD(2) isotopomers of all methyl-containing amino-acids can be observed in residually protonated samples of large proteins obtained from [U-(13)C,(1)H]-glucose/D(2)O-based bacterial media, with sensitivity sufficient for a number of NMR applications. Selective detection of some subsets of methyl groups (Ala(beta), Thr(gamma 2)) is possible using simple 'out-and-back' NMR methodology. Such selective methyl-detected 'out-and-back' NMR experiments allow complete assignments of threonine gamma 2 methyls in residually protonated, [U-(13)C,(1)H]-glucose/D(2)O-derived samples of an 82-kDa enzyme Malate Synthase G. [U-(13)C,(1)H]-glucose/D(2)O-derived protein samples are relatively inexpensive and are usually available at very early stages of any NMR study of high-molecular-weight systems.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Malate Synthase / chemistry*
  • Methylation
  • Nuclear Magnetic Resonance, Biomolecular / methods*
  • Protons*

Substances

  • Protons
  • Malate Synthase