蛋白质组学
蛋白质组
计算生物学
质谱法
定量蛋白质组学
选择性反应监测
生物
化学
生物化学
串联质谱法
色谱法
基因
作者
Masaki Matsumoto,Fumiko Matsuzaki,Kiyotaka Oshikawa,Naoki Goshima,Masatoshi Mori,Yoshifumi Kawamura,Koji Ogawa,Eriko Fukuda,Hirokazu Nakatsumi,Tohru Natsume,Kazuhiko Fukui,Katsuhisa Horimoto,Takeshi Nagashima,Ryo Funayama,Keiko Nakayama,Keiichi I. Nakayama
出处
期刊:Nature Methods
[Springer Nature]
日期:2016-12-26
卷期号:14 (3): 251-258
被引量:83
摘要
Targeted proteomics approaches are of value for deep and accurate quantification of protein abundance. Extending such methods to quantify large numbers of proteins requires the construction of predefined targeted assays. We developed a targeted proteomics platform-in vitro proteome-assisted multiple reaction monitoring (MRM) for protein absolute quantification (iMPAQT)-by using >18,000 human recombinant proteins, thus enabling protein absolute quantification on a genome-wide scale. Our platform comprises experimentally confirmed MRM assays of mass tag (mTRAQ)-labeled peptides to allow for rapid and straightforward measurement of the absolute abundance of predefined sets of proteins by mass spectrometry. We applied iMPAQT to delineate the quantitative metabolic landscape of normal and transformed human fibroblasts. Oncogenic transformation gave rise to relatively small but global changes in metabolic pathways resulting in aerobic glycolysis (Warburg effect) and increased rates of macromolecule synthesis. iMPAQT should facilitate quantitative biology studies based on protein abundance measurements.
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