Multi-target bioactive compound screening from the infructescence of Platycarya strobilacea Sieb. et Zucc. by affinity chromatography using immobilized β

ellagic acid multi-target compound screening muscarinic-3 acetylcholine receptor the infructescence of Platycarya strobilacea Sieb. et Zucc β2-adrenoceptor

Journal

Journal of separation science
ISSN: 1615-9314
Titre abrégé: J Sep Sci
Pays: Germany
ID NLM: 101088554

Informations de publication

Date de publication:
Aug 2023
Historique:
revised: 02 06 2023
received: 24 02 2023
accepted: 02 06 2023
medline: 25 8 2023
pubmed: 21 6 2023
entrez: 20 6 2023
Statut: ppublish

Résumé

As a main source for the recognition and identification of lead compounds, traditional Chinese medicine plays a pivotal role in preventing diseases for years. However, screening bioactive compounds from traditional Chinese medicine remains challenging because of the complexity of the systems and the occurrence of the synergic effect of the compounds. The infructescence of Platycarya strobilacea Sieb. et Zucc is prescribed for allergic rhinitis treatment with unknown bioactive compounds and unclear mechanisms. Herein, we immobilized the β

Identifiants

pubmed: 37339788
doi: 10.1002/jssc.202300129
doi:

Substances chimiques

Drugs, Chinese Herbal 0
Ellagic Acid 19YRN3ZS9P
Catechin 8R1V1STN48
Muscarine 7T101UWZ5W
Receptors, Cholinergic 0
Cholinergic Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2300129

Subventions

Organisme : National Natural Science Foundation of China
ID : 22004097
Organisme : National Natural Science Foundation of China
ID : 22074117
Organisme : Shaanxi Administration of Traditional Chinese Medicine
ID : 2023-ZQNY-010

Informations de copyright

© 2023 Wiley-VCH GmbH.

Références

Song HP, Zhang H, Hu R, Xiao HH, Guo H, Yuan WH, et al. A strategy to discover lead chemome from traditional Chinese medicines based on natural chromatogram-effect correlation (NCEC) and natural structure-effect correlation (NSEC): Mahonia bealei and Mahonia fortunei as a case study. J Chromatogr B. 2021;1181(1):122922.
Fu QH, Liu XM, Li Y, Wang P, Wu T, Xiao HH, et al. Discovery of new inhibitors of eEF2K from traditional Chinese medicine based on in silico screening and in vitro experimental validation. Molecules 2022;27(15):4886.
Huo XQ, Gu Y, Zhang YL, The discovery of multi-target compounds with anti-inflammation activity from traditional Chinese medicine by TCM-target effects relationship spectrum. J Ethnopharmacol. 2022;293(15):115289.
Vu H, Pham NB, Quimn RJ, Direct screening of natural product extracts using mass spectrometry. J Biomol Screen. 2008;13:265-75.
Breemen RBV, Huang CR, Nikolic D, Woodbury CP, Zhao YZ, Venton DL, Pulsed ultrafiltration mass spectrometry: a new method for screening combinatorial libraries. Anal Chem. 1997, 69: 2159-64.
Chen GL, Huang BX, Guo MQ, Current advances in screening for bioactive components from medicinal plants by affinity ultrafiltration mass spectrometry. Phytochem Anal. 2018, 29(4): 375-86.
Wan H, Rehngren M, High-throughput screening of protein binding by equilibrium dialysis combined with liquid chromatography and mass spectrometry. J Chromatogr A. 2006, 1102(1-2): 125-34.
Su XY, Kong L, Li X, Chen XG, Guo M, Zou HF, Screening and analysis of bioactive compounds with biofingerprinting chromatogram analysis of traditional Chinese medicines targeting DNA by microdialysis/HPLC. J Chromatogr A. 2005, 1076(1-2): 118-26.
Wei F, Wang SC, Gou XL, A review for cell-based screening methods in drug discovery. Biophys Rep. 2021, 7(6): 504-16.
Hage DS, High-performance affinity chromatography: a powerful tool for studying serum protein binding. J Chromatogr B. 2002, 768(1): 3-30.
Chen XF, Cao Y, Lv DY, Zhu ZY, Zhang JP, Chai YF, Comprehensive two-dimensional HepG2/cell membrane chromatography/monolithic column/time-of-flight mass spectrometry system for screening anti-tumor components from herbal medicines. J Chromatogr A. 2012, 1242: 67-74.
Sun M, Ren J, Du H, Zhang YM, Zhang J, Wang SC, et al. A combined A431 cell membrane chromatography and online high performance liquid chromatography/mass spectrometry method for screening compounds from total alkaloid of Radix caulophylli acting on the human EGFR. J Chromatogr B. 2010, 878: 2712-8.
Hou XF, Wang SC, Hou JJ, He LC, Establishment of A431 cell membrane chromatography-RPLC method for screening target components from Radix caulophylli. J Sep Sci. 2011, 34: 508-13.
Zhao XF, Li Q, Chen JJ, Xiao CN, Bian LJ, Zheng JB, et al. Exploring drug-protein interactions using the relationship between injection volume and capacity factor. J Chromatogr A. 2014, 1339: 137-44.
Zhao XF, Li Q, Xiao CN, Zhang YJ, Bian LJ, Zheng JB, et al. Oriented immobilisation of histidine-tagged protein and its application in exploring interactions between ligands and proteins. Anal Bioanal Chem. 2014, 406: 2975-85.
Zhao XF, Nan YF, Xiao CN, Zheng JB, Zheng XH, Wei YM, et al. Screening the bioactive compounds in aqueous extract of Coptidis rhizoma which specifically bind to rabbit lung tissues β2-adrenoceptor using an affinity chromatographic selection method. J Chromatogr B. 2010;878(2):2029-34
Li Q, Ning XH, An YX, Stanley BJ, Liang Y, Wang J, et al. Reliable analysis of the interaction between specific ligands and immobilized beta-2-adrenoceptor by adsorption energy distribution. Anal Chem. 2018;90(13):7903-11.
Liang Q, Fu XY, Zhang JF, Hao JX, Feng GJ, Wang J, et al. Immobilized angiotensin II type I receptor: a powerful method of high throughput screening for antihypertensive compound identification through binding interaction analysis. J Chromatogr A. 2020,1620: 461003.
Yuan XY, Shayiranbieke AEDS, Xu R, Jiang HM, Yang YS, et al. Site-selective covalently immobilized alpha 1A adrenergic receptor for thermodynamic and extra-thermodynamic study of four ligands binding to the receptor by chromatographic methods. J Chromatogr A. 2022;1665: 462827.
Zeng KZ, Li Q, Wang J, Yin GW, Zhang YJ, Xiao CN, et al. One-step methodology for the direct covalent capture of GPCRs from complex matrices onto solid surfaces based on the bioorthogonal reaction between haloalkane dehalogenase and chloroalkanes. Chem Sci. 2018;9:446-56.
Kasai K, Frontal affinity chromatography: an excellent method of analyzing weak biomolecular interactions based on a unique principle. BBA Gen Subjects. 2021;1865(1): 129761.
Tong Z, Joseph KS, Hage DS. Detection of heterogeneous drug-protein binding by frontal analysis and high-performance affinity chromatography. J Chromatogr A. 2011;1218:8915-24.
Shibukawa A, Kuroda Y, Nakagawa T, High-performance frontal analysis for drug-protein binding study. J Pharma Biomed Anal. 1999;18:1047-55.
Meng XY, Zhang HX, Mezei M, Cui M. Molecular docking: a powerful approach for structure-based drug discovery. Curr Comput Aided Drug Des. 2011;7(2):146-57.
Pinzi L, Rastelli G, Molecular docking: shifting paradigms in drug discovery. Int J Mol Sci. 2019;20(18):4331.
Miroux B, Walker JE, Over-production of proteins in Escherichia coli: mutant hosts that allow synthesis of some membrane proteins and globular proteins at high levels. J Mol Biol. 1996;260 (3):289-98.
Wiseman DN, Otchere A, Patel JH, Uddin R, Pollock NL, Routledge SJ, et al. Expression and purification of recombinant G protein-coupled receptors: a review. Protein Expres Purif. 2020;167: 105524.
Wheatley M, Hawtin SR, Glycosylation of G-protein-coupled receptors for hormones central to normal reproductive functioning: its occurrence and role, Hum Reprod Update. 1999;5(4):356-64.
Hu KX, Duan X, Han LZ, Ju HY, Wang B, Tang ZS, et al. Exploring pharmacological mechanisms of Xiang Ju Tablets in the treatment of allergic rhinitis via a network pharmacology approach. Evid Based Compl Altern Med. 2019, 6272073
Liu JK, Ying M, Wu B, Fu CM, Ethanol extract of the infructescence of Platycarya strobilacea Sieb. et Zucc. induces methuosis of human nasopharyngeal carcinoma cells. Evid Based Compl Altern Med. 2020, 2760979
Matera MG, Page C, Rinaldi B, β2-adrenoceptor signaling bias in asthma and COPD and the potential impact on the comorbidities associated with these diseases. Curr Opin Pharmacol. 2018;40:142-6.
Osborne HB, Brann MR, Pharmacology of muscarinic acetylcholine receptor subtypes (m1-m5): high throughput assays in mammalian cells, Eur J Pharmacol. 1996;295:93-102.

Auteurs

HaoSen Zhang (H)

Synthetic and Natural Functional Molecule Chemistry of Ministry of Education Key Laboratory, College of Chemistry and Materials Science, Northwest University, Xi'an, China.

Jing Wang (J)

Key Laboratory of Resource Biology and Biotechnology in Western China, College of Life Sciences, Northwest University, Xi'an, China.

Chaozhan Wang (C)

Synthetic and Natural Functional Molecule Chemistry of Ministry of Education Key Laboratory, College of Chemistry and Materials Science, Northwest University, Xi'an, China.

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Classifications MeSH