Cell permeable affinity- and activity-based probes

被引:23
作者
Jones, Lyn H. [1 ]
机构
[1] Pfizer, WorldWide Med Chem, Cambridge, MA 02139 USA
关键词
QUANTITATIVE CHEMICAL PROTEOMICS; KINASE INHIBITORS; CLICK CHEMISTRY; TERMINAL ALKYNES; IMAGING PROBES; CATHEPSIN-S; IN-VIVO; PROTEIN; TARGETS; IDENTIFICATION;
D O I
10.4155/fmc.15.100
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
Chemical biology has a significant role to play in the discovery and validation of new therapeutic targets. Activity- and affinity-based probes have demonstrated considerable promise in the drug discovery setting as they provide a chemoproteomic means to confirm and quantify target engagement and selectivity of small molecule drug candidates. Many of these technologies have been developed using cell lysate (through the use of resin-immobilized enzyme inhibitors for example), but this does not represent the biology of an intact cell. This review highlights recent advances made in the design and application of cell-permeable probes that report on target activity and drug-target occupancy in living cells, thus providing a means to decipher molecular pharmacology and pathology in a more physiologically relevant manner.
引用
收藏
页码:2131 / 2141
页数:11
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