A fluorescent probe for monitoring PTP-PEST enzymatic activity

被引:4
作者
Casey, Garrett R. [1 ,2 ]
Stains, Cliff, I [1 ,3 ,4 ,5 ,6 ]
机构
[1] Univ Nebraska, Dept Chem, Lincoln, NE 68588 USA
[2] Southeast Missouri State Univ, Dept Chem & Phys, Cape Girardeau, MO 63701 USA
[3] Univ Virginia, Dept Chem, Charlottesville, VA 22904 USA
[4] Univ Nebraska, Nebraska Ctr Integrated Biomol Commun, Lincoln, NE 68588 USA
[5] Univ Nebraska Med Ctr, Canc Genes & Mol Regulat Program, Fred & Pamela Buffet & Canc Ctr, Omaha, NE 68198 USA
[6] Univ Virginia, Canc Ctr, Charlottesville, VA 22904 USA
关键词
PROTEIN-KINASE ACTIVITY; PHOSPHATASE-ACTIVITY; TYROSINE PHOSPHATASES; CELL-MIGRATION; CANCER; DEPHOSPHORYLATION; PHOSPHORYLATION; QUANTIFICATION; MOTILITY; ADHESION;
D O I
10.1039/d0an00993h
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Phosphatase non-receptor type 12 (PTPN12 or PTP-PEST) is a critical regulator of cell migration, acting as a tumor suppressor in cancer. Decreases in PTP-PEST expression correlate with aggressive phenotypes in hepatocellular carcinoma (HCC). Despite the importance of PTP-PEST in cellular signaling, methods to directly monitor its enzymatic activity are lacking. Herein, we report the design, synthesis, and optimization of a probe to directly monitor PTP-PEST enzymatic activityviaa fluorescent readout. This activity sensor, termed pPEST1tide, is capable of detecting as little as 0.2 nM recombinant PTP-PEST. In addition, we demonstrate that this probe can selectively report on PTP-PEST activity using a panel of potential off-target enzymes. In the long-term, this activity probe could be utilized to identify small molecule modulators of PTP-PEST activity as well as provide a prognostic readout for HCC.
引用
收藏
页码:6713 / 6718
页数:6
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