¹⁵N metabolic labeling: evidence for a stable isotope effect on plasma protein levels and peptide chromatographic retention times

J Proteomics. 2013 Aug 2:88:27-33. doi: 10.1016/j.jprot.2012.12.013. Epub 2012 Dec 30.

Abstract

Many quantitative proteomics methods rely on protein and peptide labeling with stable isotopes. We have recently found that the introduction of ¹⁵N into organisms via in vivo metabolic labeling affects protein expression levels as well as metabolic pathways and behavioral phenotypes. Here, we present further evidence for a stable isotope effect based on the plasma proteome analysis of ¹⁵N-labeled mice. We compared plasma proteomes of ¹⁵N-labeled and unlabeled (¹⁴N) mice by quantitative MS. We found a number of protein level differences, some of which were verified immunochemically. In addition, we observed divergent chromatographic retention time and peak full width at half maximum (FWHM) between ¹⁵N-labeled and ¹⁴N tryptic peptides. Our data point toward a systemic effect of the introduction of heavy isotopes in vivo.

Keywords: (15)N isotope effect; (15)N metabolic labeling; C5; FWHM; HAB; Mup; Plasma; Quantitative proteomics; Serpina6; TPP; TST; XIC; complement 5; corticosteroid-binding globulin; extracted ion chromatogram; full width at half maximum; high anxiety-related behavior; major urinary protein; tail suspension test; trans-proteomic pipeline.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Proteins / chemistry
  • Blood Proteins / metabolism*
  • Chromatography, High Pressure Liquid / methods
  • Gene Expression Regulation*
  • Isotope Labeling / methods*
  • Mice
  • Nitrogen Isotopes / chemistry
  • Nitrogen Isotopes / metabolism
  • Peptides / chemistry
  • Peptides / metabolism*
  • Proteome / chemistry
  • Proteome / metabolism*
  • Proteomics / methods*

Substances

  • Blood Proteins
  • Nitrogen Isotopes
  • Peptides
  • Proteome