Metabolic labeling of mammalian organisms with stable isotopes for quantitative proteomic analysis

被引:287
作者
Wu, CC
MacCoss, MJ
Howell, KE
Matthews, DE
Yates, JR [1 ]
机构
[1] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
[2] Univ Colorado, Hlth Sci Ctr, Dept Cellular & Struct Biol, Denver, CO 80262 USA
[3] Univ Vermont, Dept Chem, Burlington, VT 05405 USA
关键词
D O I
10.1021/ac049208j
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
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.
引用
收藏
页码:4951 / 4959
页数:9
相关论文
共 47 条
  • [1] Alberts B., 2002, Molecular Biology of The Cell, V4th
  • [2] Organization of multiple cytochrome P450s with NADPH-cytochrome P450 reductase in membranes
    Backes, WL
    Kelley, RW
    [J]. PHARMACOLOGY & THERAPEUTICS, 2003, 98 (02) : 221 - 233
  • [3] UNIFORMLY C-13-LABELED ALGAL PROTEIN USED TO DETERMINE AMINO-ACID ESSENTIALITY INVIVO
    BERTHOLD, HK
    HACHEY, DL
    REEDS, PJ
    THOMAS, OP
    HOEKSEMA, S
    KLEIN, PD
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (18) : 8091 - 8095
  • [4] A proteomics strategy to elucidate functional protein-protein interactions applied to EGF signaling
    Blagoev, B
    Kratchmarova, I
    Ong, SE
    Nielsen, M
    Foster, LJ
    Mann, M
    [J]. NATURE BIOTECHNOLOGY, 2003, 21 (03) : 315 - 318
  • [5] LEAST SQUARES ANALYSIS AND SIMPLIFICATION OF MULTI-ISOTOPE MASS SPECTRA
    BRAUMAN, JI
    [J]. ANALYTICAL CHEMISTRY, 1966, 38 (04) : 607 - &
  • [6] Intracellular signaling from the endoplasmic reticulum to the nucleus
    Chapman, R
    Sidrauski, C
    Walter, P
    [J]. ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1998, 14 : 459 - 485
  • [7] Biology and function of the reversible sulfation pathway catalysed by human sulfotransferases and sulfatases
    Coughtrie, MWH
    Sharp, S
    Maxwell, K
    Innes, NP
    [J]. CHEMICO-BIOLOGICAL INTERACTIONS, 1998, 109 (1-3) : 3 - 27
  • [8] SIMPLIFIED STATISTICS FOR SMALL NUMBERS OF OBSERVATIONS
    DEAN, RB
    DIXON, WJ
    [J]. ANALYTICAL CHEMISTRY, 1951, 23 (04) : 636 - 638
  • [9] Quality control in the endoplasmic reticulum
    Ellgaard, L
    Helenius, A
    [J]. NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2003, 4 (03) : 181 - 191
  • [10] Differential stable isotope labeling of peptides for quantitation and de novo sequence derivation
    Goodlett, DR
    Keller, A
    Watts, JD
    Newitt, R
    Yi, EC
    Purvine, S
    Eng, JK
    von Haller, P
    Aebersold, R
    Kolker, E
    [J]. RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2001, 15 (14) : 1214 - 1221