Analysis of oxygen-18 labeled phosphate to study positional isotope experiments using LC-QTOF-MS

Anal Biochem. 2019 Feb 1:566:62-66. doi: 10.1016/j.ab.2018.11.001. Epub 2018 Nov 9.

Abstract

A method is proposed in this paper for the determination of oxygen-18 labeled phosphate so that positional isotope experiments using sensitive and rapid liquid chromatography-QTOF-mass spectrometry (LC-QTOF-MS) experiments can be carried out. The positional isotope exchange technique is a useful tool in understanding the mechanisms and kinetics of many enzyme-catalyzed reactions. Detection of the positions and concentration of these exchanged isotopes is the key. Gas chromatography-mass spectrometry (GC-MS) and nuclear magnetic resonance imaging are commonly used analytical techniques for measurement of 18O/16O, 31P and 15N isotope enrichment. Since these techniques either require a time-consuming derivatization step or have a limited sensitivity, an LC and accurate mass-based method for monitoring 18O/16O exchange was developed and compared with a standard GC-MS method. Our results showed that the LC-QTOF-MS method developed was not only as accurate as the standard GC-MS method, but also a sensitive and robust analytical platform for the simultaneous determination of isotope enrichment and the analysis of positional isotopes without chemical derivation. The LC-QTOF-MS method developed was successfully applied to the measurement of 18O/16O in the reversibility study of ATP hydrolysis by Lon proteases.

Keywords: (18)O/(16)O ratio; ATP hydrolysis; LC-QTOF-MS; O-18 labeled phosphate; Positional isotope exchange.

Publication types

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

MeSH terms

  • Adenosine Triphosphate / chemistry
  • Chromatography, Liquid / methods*
  • Enzyme Assays / methods
  • Mass Spectrometry / methods*
  • Oxygen Isotopes / chemistry
  • Phosphates / chemistry*
  • Protease La / chemistry*
  • Tandem Mass Spectrometry / methods*

Substances

  • Oxygen Isotopes
  • Oxygen-18
  • Phosphates
  • Adenosine Triphosphate
  • Protease La