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.
机构:
Univ Toronto, Dept Med Biophys, Toronto, ON, Canada
Ontario Canc Inst, Div Canc Genom & Proteom, Toronto, ON M4X 1K9, CanadaUniv Toronto, Dept Physiol, Toronto, ON, Canada