Mass Spectrometry-Based Proteomics in Preclinical Drug Discovery

被引:125
|
作者
Schirle, Markus [1 ]
Bantscheff, Marcus [2 ]
Kuster, Bernhard [3 ,4 ]
机构
[1] Novartis Inst BioMed Res Inc, Cambridge, MA 02139 USA
[2] Cellzome AG, D-69117 Heidelberg, Germany
[3] Tech Univ Munich, Chair Prote & Bioanalyt, D-85354 Freising Weihenstephan, Germany
[4] Ctr Integrated Prot Sci Munich, D-85354 Freising Weihenstephan, Germany
来源
CHEMISTRY & BIOLOGY | 2012年 / 19卷 / 01期
关键词
QUANTITATIVE CHEMICAL PROTEOMICS; ACTIVITY-BASED PROBES; TARGET IDENTIFICATION; PROTEIN COMPLEXES; IN-VIVO; AFFINITY PURIFICATION; BIOMARKER DISCOVERY; CELLULAR TARGETS; SMALL MOLECULES; POWERFUL TOOLS;
D O I
10.1016/j.chembiol.2012.01.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Preclinical stages in the drug discovery process require a multitude of biochemical and genetic assays in order to characterize the effects of drug candidates on cellular systems and model organisms. Early attempts to apply unbiased proteomic techniques to the identification of protein targets and off-targets as well as to elucidate the mode of action of candidate drug molecules suffered from a striking discrepancy between scientific expectations and what the technology was able to deliver at the time. Dramatic technological improvements in mass spectrometry-based proteomic and chemoproteomic strategies have radically changed this situation. This review, therefore, highlights proteomic approaches suitable for preclinical drug discovery illustrated by recent success stories.
引用
收藏
页码:72 / 84
页数:13
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