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Phosphoproteomics for the Masses

期刊

ACS CHEMICAL BIOLOGY
卷 5, 期 1, 页码 105-119

出版社

AMER CHEMICAL SOC
DOI: 10.1021/cb900277e

关键词

Protein phosphorylation; Phosphoproteomics; Shotgun proteomics; Collisional dissociation; Electron-based dissociation; Phosphopeptide enrichment; Isotope labeling; False discovery rate

资金

  1. National Science Foundation [0701846]
  2. National Institutes of Health [R01GM080148, P01GM081629]
  3. American Society of Mass Spectrometry
  4. Beckman Foundation
  5. Eli Lilly and Company
  6. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM080148, P01GM081629] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Protein phosphorylation serves as a primary mechanism of signal transduction in the cells of biological organisms. Technical advancements over the last several years in mass spectrometry now allow for the large-scale identification and quantitation of in vivo phosphorylation at unprecedented levels. These developments have occurred in the areas of sample preparation, instrumentation, quantitative methodology, and informatics so that today, 10 000-20 000 phosphorylation sites can be identified and quantified within a few weeks. With the rapid development and widespread availability of such data, its translation into biological insight and knowledge is a current obstacle. Here we present an overview of how this technology came to be and is currently applied, as well as future challenges for the field.

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