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Rapid screening of bioactive compound in Sanzi Yangqin Decoction and investigating of binding mechanism by immobilized β 2 -adrenogic receptor chromatography coupled with molecular docking

Screening bioactive compounds from traditional Chinese medicines plays pivotal role in preventing and curing diseases. Sanzi Yangqin Decoction (SYD) is a commonly used prescription for the treatment of cough, asthma and some other respiratory diseases for hundreds of years in practice. This reminds...

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Published in:Journal of pharmaceutical and biomedical analysis 2021-04, Vol.197, p.113957
Main Authors: Wang, Jing, Zhao, Xue, Yuan, Xinyi, Hao, Jiaxue, Chang, Zhongman, Li, Qian, Zhao, Xinfeng
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container_title Journal of pharmaceutical and biomedical analysis
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creator Wang, Jing
Zhao, Xue
Yuan, Xinyi
Hao, Jiaxue
Chang, Zhongman
Li, Qian
Zhao, Xinfeng
description Screening bioactive compounds from traditional Chinese medicines plays pivotal role in preventing and curing diseases. Sanzi Yangqin Decoction (SYD) is a commonly used prescription for the treatment of cough, asthma and some other respiratory diseases for hundreds of years in practice. This reminds us that there may exist some bioactive compounds strongly binding with the recognized receptors mediating these diseases like β -adrenegic receptor (β -AR). Therefore, this work intends to screen bioactive compounds from SYD and revealed the binding mechanism by immobilized β -AR chromatography and molecular docking. Taking advantages of a 3-high based enzymatic trans-methylation reaction (high speed, high specificity and high activity), the immobilization of β -AR was successfully achieved. Representative chromatographic peaks of SYD on the immobilized β -AR column was collected and recognized as rosmarinic acid and sinapine thiocyanate. Tension changes of the trachea ring showed that the two compounds were in a concentration-dependent manner when exerting their effects and the concentration ranges were 10 -10 mol/L and 10 10 mol/L, respectively. Molecular docking revealed Ser203, Ser204, Ser207, Tyr316 and Asn312 were the main residues for the two compounds to bind with β -AR. We concluded that the proposed method is becoming an alternative in rapid recognizing bioactive compounds from complex matrix.
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Sanzi Yangqin Decoction (SYD) is a commonly used prescription for the treatment of cough, asthma and some other respiratory diseases for hundreds of years in practice. This reminds us that there may exist some bioactive compounds strongly binding with the recognized receptors mediating these diseases like β -adrenegic receptor (β -AR). Therefore, this work intends to screen bioactive compounds from SYD and revealed the binding mechanism by immobilized β -AR chromatography and molecular docking. Taking advantages of a 3-high based enzymatic trans-methylation reaction (high speed, high specificity and high activity), the immobilization of β -AR was successfully achieved. Representative chromatographic peaks of SYD on the immobilized β -AR column was collected and recognized as rosmarinic acid and sinapine thiocyanate. Tension changes of the trachea ring showed that the two compounds were in a concentration-dependent manner when exerting their effects and the concentration ranges were 10 -10 mol/L and 10 10 mol/L, respectively. Molecular docking revealed Ser203, Ser204, Ser207, Tyr316 and Asn312 were the main residues for the two compounds to bind with β -AR. We concluded that the proposed method is becoming an alternative in rapid recognizing bioactive compounds from complex matrix.</description><identifier>EISSN: 1873-264X</identifier><identifier>DOI: 10.1016/j.jpba.2021.113957</identifier><identifier>PMID: 33601158</identifier><language>eng</language><publisher>England</publisher><ispartof>Journal of pharmaceutical and biomedical analysis, 2021-04, Vol.197, p.113957</ispartof><rights>Copyright © 2021 Elsevier B.V. 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title Rapid screening of bioactive compound in Sanzi Yangqin Decoction and investigating of binding mechanism by immobilized β 2 -adrenogic receptor chromatography coupled with molecular docking
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