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In situ synthesis and unidirectional insertion of membrane proteins in liposome-immobilized silica stationary phase for rapid preparation of microaffinity chromatography

Cell membrane affinity chromatography has been widely applied in membrane protein (MP)-targeted drug screening and interaction analysis. However, in current methods, the MP sources are derived from cell lines or recombinant protein expression, which are time-consuming for cell culture or purificatio...

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Autores principales: Gu, Yanqiu, Wang, Rong, Chen, Panpan, Li, Shengnan, Chai, Xinyi, Chen, Chun, Liu, Yue, Cao, Yan, Lv, Diya, Hong, Zhanying, Zhu, Zhenyu, Chai, Yifeng, Yuan, Yongfang, Chen, Xiaofei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9513493/
https://www.ncbi.nlm.nih.gov/pubmed/36176904
http://dx.doi.org/10.1016/j.apsb.2022.04.010
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author Gu, Yanqiu
Wang, Rong
Chen, Panpan
Li, Shengnan
Chai, Xinyi
Chen, Chun
Liu, Yue
Cao, Yan
Lv, Diya
Hong, Zhanying
Zhu, Zhenyu
Chai, Yifeng
Yuan, Yongfang
Chen, Xiaofei
author_facet Gu, Yanqiu
Wang, Rong
Chen, Panpan
Li, Shengnan
Chai, Xinyi
Chen, Chun
Liu, Yue
Cao, Yan
Lv, Diya
Hong, Zhanying
Zhu, Zhenyu
Chai, Yifeng
Yuan, Yongfang
Chen, Xiaofei
author_sort Gu, Yanqiu
collection PubMed
description Cell membrane affinity chromatography has been widely applied in membrane protein (MP)-targeted drug screening and interaction analysis. However, in current methods, the MP sources are derived from cell lines or recombinant protein expression, which are time-consuming for cell culture or purification, and also difficult to ensure the purity and consistent orientation of MPs in the chromatographic stationary phase. In this study, a novel in situ synthesis membrane protein affinity chromatography (iSMAC) method was developed utilizing cell-free protein expression (CFE) and covalent immobilized affinity chromatography, which achieved efficient in situ synthesis and unidirectional insertion of MPs into liposomes in the stationary phase. The advantages of iSMAC are: 1) There is no need to culture cells or prepare recombinant proteins; 2) Specific and purified MPs with stable and controllable content can be obtained within 2 h; 3) MPs maintain the transmembrane structure and a consistent orientation in the chromatographic stationary phase; 4) The flexible and personalized construction of cDNAs makes it possible to analyze drug binding sites. iSMAC was successfully applied to screen PDGFRβ inhibitors from Salvia miltiorrhiza and Schisandra chinensis. Micro columns prepared by in-situ synthesis maintain satisfactory analysis activity within 72 h. Two new PDGFRβ inhibitors, salvianolic acid B and gomisin D, were screened out with K(D) values of 13.44 and 7.39 μmol/L, respectively. In vitro experiments confirmed that the two compounds decreased α-SMA and collagen Ӏ mRNA levels raised by TGF-β in HSC-T6 cells through regulating the phosphorylation of p38, AKT and ERK. In vivo, Sal B could also attenuate CCl(4)-induced liver fibrosis by downregulating PDGFRβ downstream related protein levels. The iSMAC method can be applied to other general MPs, and provides a practical approach for the rapid preparation of MP-immobilized or other biological solid-phase materials.
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spelling pubmed-95134932022-09-28 In situ synthesis and unidirectional insertion of membrane proteins in liposome-immobilized silica stationary phase for rapid preparation of microaffinity chromatography Gu, Yanqiu Wang, Rong Chen, Panpan Li, Shengnan Chai, Xinyi Chen, Chun Liu, Yue Cao, Yan Lv, Diya Hong, Zhanying Zhu, Zhenyu Chai, Yifeng Yuan, Yongfang Chen, Xiaofei Acta Pharm Sin B Original Article Cell membrane affinity chromatography has been widely applied in membrane protein (MP)-targeted drug screening and interaction analysis. However, in current methods, the MP sources are derived from cell lines or recombinant protein expression, which are time-consuming for cell culture or purification, and also difficult to ensure the purity and consistent orientation of MPs in the chromatographic stationary phase. In this study, a novel in situ synthesis membrane protein affinity chromatography (iSMAC) method was developed utilizing cell-free protein expression (CFE) and covalent immobilized affinity chromatography, which achieved efficient in situ synthesis and unidirectional insertion of MPs into liposomes in the stationary phase. The advantages of iSMAC are: 1) There is no need to culture cells or prepare recombinant proteins; 2) Specific and purified MPs with stable and controllable content can be obtained within 2 h; 3) MPs maintain the transmembrane structure and a consistent orientation in the chromatographic stationary phase; 4) The flexible and personalized construction of cDNAs makes it possible to analyze drug binding sites. iSMAC was successfully applied to screen PDGFRβ inhibitors from Salvia miltiorrhiza and Schisandra chinensis. Micro columns prepared by in-situ synthesis maintain satisfactory analysis activity within 72 h. Two new PDGFRβ inhibitors, salvianolic acid B and gomisin D, were screened out with K(D) values of 13.44 and 7.39 μmol/L, respectively. In vitro experiments confirmed that the two compounds decreased α-SMA and collagen Ӏ mRNA levels raised by TGF-β in HSC-T6 cells through regulating the phosphorylation of p38, AKT and ERK. In vivo, Sal B could also attenuate CCl(4)-induced liver fibrosis by downregulating PDGFRβ downstream related protein levels. The iSMAC method can be applied to other general MPs, and provides a practical approach for the rapid preparation of MP-immobilized or other biological solid-phase materials. Elsevier 2022-09 2022-04-22 /pmc/articles/PMC9513493/ /pubmed/36176904 http://dx.doi.org/10.1016/j.apsb.2022.04.010 Text en © 2022 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Gu, Yanqiu
Wang, Rong
Chen, Panpan
Li, Shengnan
Chai, Xinyi
Chen, Chun
Liu, Yue
Cao, Yan
Lv, Diya
Hong, Zhanying
Zhu, Zhenyu
Chai, Yifeng
Yuan, Yongfang
Chen, Xiaofei
In situ synthesis and unidirectional insertion of membrane proteins in liposome-immobilized silica stationary phase for rapid preparation of microaffinity chromatography
title In situ synthesis and unidirectional insertion of membrane proteins in liposome-immobilized silica stationary phase for rapid preparation of microaffinity chromatography
title_full In situ synthesis and unidirectional insertion of membrane proteins in liposome-immobilized silica stationary phase for rapid preparation of microaffinity chromatography
title_fullStr In situ synthesis and unidirectional insertion of membrane proteins in liposome-immobilized silica stationary phase for rapid preparation of microaffinity chromatography
title_full_unstemmed In situ synthesis and unidirectional insertion of membrane proteins in liposome-immobilized silica stationary phase for rapid preparation of microaffinity chromatography
title_short In situ synthesis and unidirectional insertion of membrane proteins in liposome-immobilized silica stationary phase for rapid preparation of microaffinity chromatography
title_sort in situ synthesis and unidirectional insertion of membrane proteins in liposome-immobilized silica stationary phase for rapid preparation of microaffinity chromatography
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9513493/
https://www.ncbi.nlm.nih.gov/pubmed/36176904
http://dx.doi.org/10.1016/j.apsb.2022.04.010
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