Development of Neh2-Luciferase Reporter and Its Application for High Throughput Screening and Real-Time Monitoring of Nrf2 Activators

被引:94
作者
Smirnova, Natalya A. [1 ]
Haskew-Layton, Renee E. [1 ]
Basso, Manuela [1 ]
Hushpulian, Dmitry M. [2 ]
Payappilly, Jimmy B. [1 ]
Speer, Rachel E. [1 ]
Ahn, Young-Hoon [3 ]
Rakhman, Ilay [1 ]
Cole, Philip A. [3 ]
Pinto, John T. [4 ]
Ratan, Rajiv R. [1 ]
Gazaryan, Irina G. [1 ]
机构
[1] Cornell Univ, Weill Med Coll, Burke Med Res Inst, Dept Neurol & Neurosci, White Plains, NY 10605 USA
[2] Moscow MV Lomonosov State Univ, Sch Chem, Dept Enzymol, Moscow 119992, Russia
[3] Johns Hopkins Univ, Sch Med, Dept Pharmacol & Mol Sci, Baltimore, MD 21205 USA
[4] New York Med Coll, Dept Biochem & Mol Biol, Valhalla, NY 10595 USA
来源
CHEMISTRY & BIOLOGY | 2011年 / 18卷 / 06期
关键词
TRANSCRIPTION FACTOR NRF2; NRF2-MEDIATED ANTIOXIDANT RESPONSE; OXIDATIVE-STRESS-RESPONSE; CUL3-BASED E3 LIGASE; IN-VIVO; CEREBRAL-ISCHEMIA; SIGNALING PATHWAY; RECOGNITION MODEL; PROTECTS NEURONS; HSP90; INHIBITOR;
D O I
10.1016/j.chembiol.2011.03.013
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
The NF-E2-related factor 2 (Nrf2) is a key transcriptional regulator of antioxidant defense and detoxification. To directly monitor stabilization of Nrf2, we fused its Neh2 domain, responsible for the interaction with its nucleocytoplasmic regulator, Keap1, to firefly luciferase (Neh2-luciferase). We show that Neh2 domain is sufficient for recognition, ubiquitination, and proteasomal degradation of Neh2-luciferase fusion protein. The Neh2-luc reporter system allows direct monitoring of the adaptive response to redox stress and classification of drugs based on the time course of reporter activation. The reporter was used to screen the Spectrum library of 2000 biologically active compounds to identify activators of Nrf2. The most robust and yet nontoxic Nrf2 activators found-nordihydroguaiaretic acid, fisetin, and gedunin-induced astrocyte-dependent neuroprotection from oxidative stress via an Nrf2-dependent mechanism.
引用
收藏
页码:752 / 765
页数:14
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