In-gel activity-based protein profiling of a clickable covalent ERK1/2 inhibitor

被引:16
|
作者
Lebraud, Honorine [1 ]
Wright, David J. [1 ]
East, Charlotte E. [1 ]
Holding, Finn P. [1 ]
O'Reilly, Marc [1 ]
Heightman, Tom D. [1 ]
机构
[1] Astex Pharmaceut, 436 Cambridge Sci Pk, Cambridge CB4 0QA, England
关键词
CHEMICAL PROBES; LIVING CELLS; LIVE CELLS; DISCOVERY; KINASE; TETRAZINE; SELECTIVITY; CHEMISTRY; MECHANISM; LIGATION;
D O I
10.1039/c6mb00367b
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
In-gel activity-based protein profiling (ABPP) offers rapid assessment of the proteome-wide selectivity and target engagement of a chemical tool. Here we demonstrate the use of the inverse electron demand Diels Alder (IEDDA) click reaction for in-gel ABPP by evaluating the selectivity profile and target engagement of a covalent ERK1/2 probe tagged with a trans-cyclooctene group. The chemical probe was shown to bind covalently to Cys166 of ERK2 using protein MS and X-ray crystallography, and displayed submicromolar GI(50)s in A375 and HCT116 cells. In both cell lines, the probe demonstrated target engagement and a good selectivity profile at low concentrations, which was lost at higher concentrations. The IEDDA cycloaddition enabled fast and quantitative fluorescent tagging for readout with a high background-to-noise ratio and thereby provides a promising alternative to the commonly used copper catalysed alkyne-azide cycloaddition.
引用
收藏
页码:2867 / 2874
页数:8
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