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Development of a fluorescence polarization-based high-throughput screening assay to identify antagonists targeting β-catenin/TCF4 interaction
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Yun-yu CHEN1, Ke HU1, Zheng-hao FU1, Xia-yi NIU1, Jing ZHANG2, *, Xiao-ping LIU1, *
Acta Pharmaceutica Sinica | 2020, 55(5) : 884 - 891
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Acta Pharmaceutica Sinica | 2020, 55(5): 884-891
Original Articles
Development of a fluorescence polarization-based high-throughput screening assay to identify antagonists targeting β-catenin/TCF4 interaction
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Yun-yu CHEN1, Ke HU1, Zheng-hao FU1, Xia-yi NIU1, Jing ZHANG2, *, Xiao-ping LIU1, *
Affiliations
  • 1. Institute for Drug Screening and Evaluation, Wannan Medical College, Wuhu 241002, China
  • 2. Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China
Published: 2020-05-12 doi: 10.16438/j.0513-4870.2019-0998
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To develop a fluorescence polarization (FP)-based high-throughput screening (HTS) assay to identify novel small-molecule antagonists targeting β-catenin/TCF4 (T-cell factor 4) interaction, recombinant human β-catenin was expressed in Escherichia coli Rosetta (DE3) cells and purified by HisTrapTM column. The bioactivity of purified β-catenin was further analyzed by enzyme-linked immunosorbent assay (ELISA). According to FP principle, the β-catenin/TCF4 binding model was performed, and fluorescence isothiocyanate (FITC) labeled TCF4 peptide (FITC-TCF4) served as the molecular probe of adaptor for binding to β-catenin. The FITC-TCF4 and β-catenin working concentration were optimized, and the binding conditions (complex stability and dimethylsulfoxide (DMSO) tolerance) have been investigated yet for further hits screening. The results showed that recombinant human β-catenin was successfully expressed and purified β-catenin exhibited favorable bioactivity in ELISA binding assay. Subsequently, the FP-based HTS assay was performed using 20 nmol·L-1 FITC-TCF4 and 100 nmol·L-1 β-catenin. Under these optimized conditions, a high Zxfactor of 0.88 was achieved in a 384-well format and this FP-based HTS assay was very stable with regard to DMSO. Through screening of a natural-based product library (NBPL) using the established FP-based HTS assay, three hits (sanguinarine, chelerythrine, and compound S720) were identified as potential β-catenin/TCF4 interaction antagonists. Taken together, we have successfully developed a simple, robust and reliable FP-based HTS assay for screening of novel antagonists targeting β-catenin/TCF4 interaction.

Wnt inhibitor  /  β-catenin/TCF4 interaction  /  fluorescence polarization  /  high-throughput screening  /  sanguinarine  /  chelerythrine
Yun-yu CHEN, Ke HU, Zheng-hao FU, Xia-yi NIU, Jing ZHANG, Xiao-ping LIU. Development of a fluorescence polarization-based high-throughput screening assay to identify antagonists targeting β-catenin/TCF4 interaction[J]. Acta Pharmaceutica Sinica, 2020 , 55 (5) : 884 -891 . DOI: 10.16438/j.0513-4870.2019-0998
Year 2020 volume 55 Issue 5
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Article Info
doi: 10.16438/j.0513-4870.2019-0998
  • Receive Date:2019-12-06
  • Online Date:2026-01-21
  • Published:2020-05-12
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  • Received:2019-12-06
  • Revised:2020-01-16
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    1. Institute for Drug Screening and Evaluation, Wannan Medical College, Wuhu 241002, China
    2. Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China
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表12种不同金属材料的力学参数

Family
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Number of
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Number of
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鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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