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Identification of novel selective TRPV3 antagonists based on virtual screening, molecular docking and bioassay
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Yan-jun SHEN, Xin-ran ZHANG, Yang WU, Ke-wei WANG, Zhen-ming LIU, Hong-wei JIN*, Liang-ren ZHANG*, Li-he ZHANG
Acta Pharmaceutica Sinica | 2018, 53(6) : 966 - 975
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Acta Pharmaceutica Sinica | 2018, 53(6): 966-975
Medicinal Chemistry Medicinal Chemistry
Identification of novel selective TRPV3 antagonists based on virtual screening, molecular docking and bioassay
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Yan-jun SHEN, Xin-ran ZHANG, Yang WU, Ke-wei WANG, Zhen-ming LIU, Hong-wei JIN*, Liang-ren ZHANG*, Li-he ZHANG
Affiliations
  • State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing 100191, China
Published: 2018-06-12 doi: 10.16438/j.0513-4870.2018-0047
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Transient receptor potential vanilloid member 3 (TRPV3) is a temperature-sensitive cation channel protein, which contributes to nociception, itch, hair growth, emotional control and the pathophysiology of migraine. However, research progress on TRPV3 fundamental molecular biology is rather slow, compared to other TRP channels due to the lack of its selective antagonists. It's necessary to identify TRPV3 selective antagonists for the study on TRPV3 physiological functions. In this study, several selective TRPV3 antagonists were identified by ligand-based virtual screening of shape-based similarity and electrostatic matching. The most potent one (V-39) blocked 2-APB-activated currents in a stable human TRPV3 expressed HEK293T cell line with IC50=18.0 ±1.1 μmol·L-1 (n=4). Besides, the interaction pattern between TRPV3 and its antagonists were studied through docking the antagonists into a homology model (TRPV3_HM4) generated from the crystal structure of TPRV1. The docking results show that the binding site of TRPV3 locates between linker domain (of N-terminus and TM1) and TRP Box. There are a π-π stacking interaction and hydrogen bonding interactions between compound V-39 and residues His-310, His-314 and Arg-577 of the pocket. Identification of these antagonists provides new probes for understanding the pharmacological function of TRPV3 channel.

virtual screening  /  TRPV3  /  antagonist  /  selectivity  /  docking
Yan-jun SHEN, Xin-ran ZHANG, Yang WU, Ke-wei WANG, Zhen-ming LIU, Hong-wei JIN, Liang-ren ZHANG, Li-he ZHANG. Identification of novel selective TRPV3 antagonists based on virtual screening, molecular docking and bioassay[J]. Acta Pharmaceutica Sinica, 2018 , 53 (6) : 966 -975 . DOI: 10.16438/j.0513-4870.2018-0047
Year 2018 volume 53 Issue 6
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doi: 10.16438/j.0513-4870.2018-0047
  • Receive Date:2018-01-12
  • Online Date:2026-01-15
  • Published:2018-06-12
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  • Received:2018-01-12
  • Revised:2018-02-21
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    State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing 100191, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
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Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
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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