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Quantitative analysis of highly homologous proteins: the challenge of assaying the CYP-ome by mass spectrometry

期刊

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
卷 392, 期 6, 页码 1123-1134

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-008-2407-z

关键词

Proteomics; Quantification; Protein label; Mass spectrometry; Target compound analysis

资金

  1. German Ministry of Education and Research (BMBF) [0313080J]
  2. Universite de Montreal, Canada
  3. University of Bochum

向作者/读者索取更多资源

Cytochrome P450 enzymes comprise families of highly homologous proteins. These proteins play a pivotal role in oxidative drug metabolism and are important targets in drug discovery research. Proteomics today is a valuable tool for the analysis of proteins. In the past, qualitative analysis of the proteome was the main focus of research, but in the last few years interest in the mathematical modelling of protein networks has been growing and so has the demand on quantitative proteome analysis. As a thorough understanding of cytochrome P450 dependent metabolism is crucial for drug discovery, it is thus not astounding that cytochrome P450 enzymes are a target for quantitative proteomics research. In this article, we review the techniques available for quantitative proteome analysis and to what extent these techniques have been used for the quantification of cytochrome P450 enzymes and give a brief outlook of the techniques that have promising potential for the analysis of these proteins in the future.

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