| Literature DB >> 23279933 |
Christian Webhofer1, Yaoyang Zhang, Jan Brusis, Stefan Reckow, Rainer Landgraf, Giuseppina Maccarrone, Christoph W Turck, Michaela D Filiou.
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.Entities:
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
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Year: 2012 PMID: 23279933 DOI: 10.1016/j.jprot.2012.12.013
Source DB: PubMed Journal: J Proteomics ISSN: 1874-3919 Impact factor: 4.044