Xu Ji, Liangxi Li, Kaiyue Zhang, Xinyi Yuan, Xiaoying Zhang, Lu Wang, Qin Zhao
{"title":"通过Colicin L7 dna酶/免疫蛋白7超亲和系统,发现桂枝茯苓方α - 1a -肾上腺素能受体结合的活性化合物并揭示其相互作用","authors":"Xu Ji, Liangxi Li, Kaiyue Zhang, Xinyi Yuan, Xiaoying Zhang, Lu Wang, Qin Zhao","doi":"10.1002/jssc.70053","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>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.</p>\n </div>","PeriodicalId":17098,"journal":{"name":"Journal of separation science","volume":"47 23","pages":""},"PeriodicalIF":2.8000,"publicationDate":"2024-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"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\",\"authors\":\"Xu Ji, Liangxi Li, Kaiyue Zhang, Xinyi Yuan, Xiaoying Zhang, Lu Wang, Qin Zhao\",\"doi\":\"10.1002/jssc.70053\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n <p>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.</p>\\n </div>\",\"PeriodicalId\":17098,\"journal\":{\"name\":\"Journal of separation science\",\"volume\":\"47 23\",\"pages\":\"\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2024-12-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of separation science\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/jssc.70053\",\"RegionNum\":3,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of separation science","FirstCategoryId":"5","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jssc.70053","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
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
In this work, Guizhi Fuling Formula (GFF), as well as α1A-adrenergic receptor (α1A-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 α1A-AR was oriented immobilized to the Im7-coated silica gel surface. With the α1A-AR immobilized column in hand, the active compounds in GFF targeted to α1A-AR were screened, and the binding procedures were analyzed. The composite characterization demonstrated that the α1A-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 α1A-AR. Among them, cinnamic acid and paeonol have the same binding site on α1A-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 α1A-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.
期刊介绍:
The Journal of Separation Science (JSS) is the most comprehensive source in separation science, since it covers all areas of chromatographic and electrophoretic separation methods in theory and practice, both in the analytical and in the preparative mode, solid phase extraction, sample preparation, and related techniques. Manuscripts on methodological or instrumental developments, including detection aspects, in particular mass spectrometry, as well as on innovative applications will also be published. Manuscripts on hyphenation, automation, and miniaturization are particularly welcome. Pre- and post-separation facets of a total analysis may be covered as well as the underlying logic of the development or application of a method.