Abstract

To quantify proteins on a global level from mammalian tissue, a method was developed to metabolically introduce 15N stable isotopes into the proteins of Rattus norvegicus for use as internal standards. The long-term metabolic labeling of rats with a diet enriched in 15N did not result in adverse health consequences. The average 15N amino acid enrichments reflected the relative turnover rates in the different tissues and ranged from 74.3 mpe in brain to 92.2 mpe in plasma. Using the 15N-enriched liver as a quantitative internal standard, changes in individual protein levels in response to cycloheximide treatment were measured for 310 proteins. These measurements revealed 127 proteins with altered protein level (p < 0.05). Most proteins with altered level have previously reported functions involving xenobiotic metabolism and protein-folding machinery of the endoplasmic reticulum. This approach is a powerful tool for the global quantitation of proteins, is capable of measuring proteome-wide changes in response to a drug, and will be useful for studying animal models of disease.

Keywords

ChemistryProteomeEndoplasmic reticulumBiochemistryXenobioticDrug metabolismCycloheximideMetabolismBlood proteinsProtein turnoverProtein biosynthesisEnzyme

Affiliated Institutions

Related Publications

Publication Info

Year
2004
Type
article
Volume
76
Issue
17
Pages
4951-4959
Citations
377
Access
Closed

External Links

Social Impact

Social media, news, blog, policy document mentions

Citation Metrics

377
OpenAlex

Cite This

Kathryn E. Howell, Dwight E. Matthews, John R. Yates et al. (2004). Metabolic Labeling of Mammalian Organisms with Stable Isotopes for Quantitative Proteomic Analysis. Analytical Chemistry , 76 (17) , 4951-4959. https://doi.org/10.1021/ac049208j

Identifiers

DOI
10.1021/ac049208j