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A time-resolved fluorescence resonance energy transfer screening assay for discovery of protein-protein interaction modulators
被引:3
|作者:
Tang, Cong
[1
,2
,6
]
Niu, Qiankun
[1
]
Cicka, Danielle
[1
]
Du, Yuhong
[1
,3
]
Mo, Xiulei
[1
]
Fu, Haian
[1
,3
,4
,5
]
机构:
[1] Emory Univ, Sch Med, Dept Pharmacol & Chem Biol, Atlanta, GA 30322 USA
[2] Xi An Jiao Tong Univ, Affiliated Hosp 1, Med Sch, Xian 710061, Peoples R China
[3] Emory Univ, Sch Med, Emory Chem Biol Discovery Ctr, Atlanta, GA 30322 USA
[4] Emory Univ, Winship Canc Inst, Dept Hematol & Med Oncol, Atlanta, GA 30322 USA
[5] Emory Univ, Winship Canc Inst, Atlanta, GA 30322 USA
[6] Univ Lisbon, Fac Med, Inst Med Mol, Ave Prof Egas Moniz, P-1649028 Lisbon, Portugal
来源:
关键词:
Cancer;
High Throughput Screening;
Molecular/Chemical Probes;
D O I:
10.1016/j.xpro.2021.100804
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Protein-protein interactions (PPIs) have emerged as promising yet challenging therapeutic targets. A robust bioassay is required for rapid PPI modulator discovery. Here, we present a time-resolved Forster's (fluorescence) resonance energy transfer assay protocol for PPI modulator screening in a 1536-well plate format. We use hypomorph SMAD4R361H-SMAD3 PPI as an example to illustrate the application of the protocol for screening of variant-directed PPI inducers. This platform can be readily adapted for the discovery of both small-molecule PPI inducers and inhibitors.For complete details on the use and execution of this protocol, please refer to Tang et al. (2020).
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页数:15
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