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A protocol for high-throughput screening of histone lysine demethylase 4 inhibitors using TR-FRET assay
被引:2
|作者:
Wu, Qiong
[1
]
Lin, Wenwei
[2
]
Li, Zhen-Mei
[3
]
Rankovic, Zoran
[2
]
White, Stephen W.
[3
,4
]
Chen, Taosheng
[2
]
Yang, Jun
[1
]
机构:
[1] St Jude Childrens Res Hosp, Dept Surg, 262 Danny Thomas Pl, Memphis, TN 38105 USA
[2] St Jude Childrens Res Hosp, Dept Chem Biol & Therapeut, 262 Danny Thomas Pl, Memphis, TN 38105 USA
[3] St Jude Childrens Res Hosp, Dept Struct Biol, 262 Danny Thomas Pl, Memphis, TN 38105 USA
[4] St Jude Childrens Res Hosp, Grad Sch Biomed Sci, 262 Danny Thomas Pl, Memphis, TN 38105 USA
来源:
关键词:
Cancer;
Chemistry;
High Throughput Screening;
Molecular/Chemical Probes;
Protein Biochemistry;
Protein expression and purification;
Structural Biology;
D O I:
10.1016/j.xpro.2021.100702
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Identification of diverse chemotypes of selective KDM4 inhibitors is important for exploring and validating the roles of KDM4s in the pathogenesis of human disease and for developing therapies. Here, we report a protocol for high -throughput screening of KDM4 inhibitors using TR-FRET demethylation func-tional assay. We describe this protocol for screen of KDM4B inhibitors, which can be modified to screen inhibitors of other JmjC-domain-containing KDMs. For complete details on the use and execution of this protocol, please refer to Singh et al. (2021).
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页数:10
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