Isozyme-Specific Fluorescent Inhibitor of Glutathione S-Transferase Omega 1

被引:36
|
作者
Son, Junghyun [1 ]
Lee, Jae-Jung [1 ]
Lee, Jun-Seok [2 ]
Schueller, Andreas [3 ]
Chang, Young-Tae [1 ,4 ]
机构
[1] Agcy Sci Technol & Res, Biomed Res Council, Singapore Bioimaging Consortium, Lab Bioimaging Probe Dev, Singapore 138667, Singapore
[2] NYU, Dept Chem, New York, NY 10003 USA
[3] Duke NUS Grad Med Sch, NUS Med Chem Programme, Singapore 269857, Singapore
[4] Natl Univ Singapore, Dept Chem, Singapore 117543, Singapore
关键词
PROTEIN;
D O I
10.1021/cb100007s
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
Recently, the glutathione S-transferase omega 1 (GSTO1) is suspected to be involved in certain cancers and neurodegenerative diseases. However, profound investigation on the pathological roles of GSTO1 has been hampered by the lack of specific methods to determine or modulate its activity in biological systems containing other isoforms with similar catalytic function. Here, we report a fluorescent compound that is able to inhibit and monitor the activity of GSTO1. We screened 43 fluorescent chemicals and found a compound (6) that binds specifically to the active site of GSTO1. We observed that compound 6 inhibits GSTO1 by covalent modification but spares other isoforms in HEK293 cells and demonstrated that compound 6 could report the activity of GSTO1 in NIH/3T3 or HEK293 cells by measuring the fluorescence intensity of the labeled amount of GSTO1 in SDS PAGE. Compound 6 is a useful tool to study GSTO1, applicable as a specific inhibitor and an activity reporter.
引用
收藏
页码:449 / 453
页数:5
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