Discovering the Bioactive Compounds Binding to α<sub>1A</sub>‐Adrenergic Receptor in Guizhi Fuling Formula and Revealing Their Interactions by Immobilizing the Receptor Through Colicin L7 DNase/Immunity Protein 7 Ultra‐Affinity System

In this work, Guizhi Fuling Formula (GFF), as well as α<sub>1A</sub>-adrenergic receptor (α<sub>1A</sub>-AR) were taken as the research objects. By utilizing the ultra-affinity between Colicin L7 DNase (CL7) and its homologous immune protein 7 (Im7), CL7-tagged α<sub>1A</sub>-AR was oriented immobilized to the Im7-coated silica gel surface. With the α<sub>1A</sub>-AR immobilized column in hand, the active compounds in GFF targeted to α<sub>1A</sub>-AR were screened, and the binding procedures were analyzed. The composite characterization demonstrated that the α<sub>1A</sub>-AR can be immobilized to the chromatographic stationary phase with good specificity and stability in 3 weeks. Paeoniflorin, cinnamic acid, and paeonol were identified as the active compounds in GFF targeted to α<sub>1A</sub>-AR. Among them, cinnamic acid and paeonol have the same binding site on α<sub>1A</sub>-AR as the specific drug tamsulosin. The binding parameters obtained by frontal analysis and injection amount-dependent analysis were consistent in the same concentration range. Collectively, these results indicated that the α<sub>1A</sub>-AR chromatographic column synthesized by a novel immobilized method was capable of screening and analyzing the functional compounds from the complex matrix, which provided an alternative for rapid screening and analysis to traditional ethnic drugs.

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Publication Details

Journal
Journal of Separation Science
Published
2024-12-01
DOI
https://doi.org/10.1002/jssc.70053
Citations
2
Primary Topic
Pharmacological Effects of Natural Compounds
Type
article
Field-Weighted Citation Impact
0.93
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article

Discovering the Bioactive Compounds Binding to α1A‐Adrenergic Receptor in Guizhi Fuling Formula and Revealing Their Interactions by Immobilizing the Receptor Through Colicin L7 DNase/Immunity Protein 7 Ultra‐Affinity System

Xinyi Yuan, Kaiyue Zhang, Qin Zhao, Xu Ji et al.
2 citations
Journal of Separation Science
Pharmacological Effects of Natural Compounds
0.93
article

Discovering the Bioactive Compounds Binding to α1A‐Adrenergic Receptor in Guizhi Fuling Formula and Revealing Their Interactions by Immobilizing the Receptor Through Colicin L7 DNase/Immunity Protein 7 Ultra‐Affinity System

Xinyi Yuan, Kaiyue Zhang, Qin Zhao, Xu Ji, Liangxi Li, Xiaoying Zhang, Lu Wang
article en
2 citations

Abstract

In this work, Guizhi Fuling Formula (GFF), as well as α<sub>1A</sub>-adrenergic receptor (α<sub>1A</sub>-AR) were taken as the research objects. By utilizing the ultra-affinity between Colicin L7 DNase (CL7) and its homologous immune protein 7 (Im7), CL7-tagged α<sub>1A</sub>-AR was oriented immobilized to the Im7-coated silica gel surface. With the α<sub>1A</sub>-AR immobilized column in hand, the active compounds in GFF targeted to α<sub>1A</sub>-AR were screened, and the binding procedures were analyzed. The composite characterization demonstrated that the α<sub>1A</sub>-AR can be immobilized to the chromatographic stationary phase with good specificity and stability in 3 weeks. Paeoniflorin, cinnamic acid, and paeonol were identified as the active compounds in GFF targeted to α<sub>1A</sub>-AR. Among them, cinnamic acid and paeonol have the same binding site on α<sub>1A</sub>-AR as the specific drug tamsulosin. The binding parameters obtained by frontal analysis and injection amount-dependent analysis were consistent in the same concentration range. Collectively, these results indicated that the α<sub>1A</sub>-AR chromatographic column synthesized by a novel immobilized method was capable of screening and analyzing the functional compounds from the complex matrix, which provided an alternative for rapid screening and analysis to traditional ethnic drugs.

Journal of Separation ScienceVol. 47(23)
Xizang Minzu University (CN)
Openalex Percentile: Top 23%
Pharmacological Effects of Natural Compounds
0.93
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