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Rapid Screening and Identification of Antitumor Ingredients from the Mangrove Endophytic Fungus Using an Enzyme-Immobilized Magnetic Nanoparticulate System

As a consequence of recent progression in biomedicine and nanotechnology, nanoparticle-based systems have evolved as a new method with extensive applications in responsive therapy, multimodal imaging, drug delivery and natural product separation. Meanwhile, the magnetic nanoparticulate system has ar...

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Autores principales: Wei, Nan, Zhao, Jun, Wu, Guimei, Cao, Wenjuan, Luo, Pei, Zhang, Zhifeng, Chen, Gang, Wen, Lu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8069786/
https://www.ncbi.nlm.nih.gov/pubmed/33924693
http://dx.doi.org/10.3390/molecules26082255
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author Wei, Nan
Zhao, Jun
Wu, Guimei
Cao, Wenjuan
Luo, Pei
Zhang, Zhifeng
Chen, Gang
Wen, Lu
author_facet Wei, Nan
Zhao, Jun
Wu, Guimei
Cao, Wenjuan
Luo, Pei
Zhang, Zhifeng
Chen, Gang
Wen, Lu
author_sort Wei, Nan
collection PubMed
description As a consequence of recent progression in biomedicine and nanotechnology, nanoparticle-based systems have evolved as a new method with extensive applications in responsive therapy, multimodal imaging, drug delivery and natural product separation. Meanwhile, the magnetic nanoparticulate system has aroused great interest for separation and purification because of its excellent magnetic properties. Phospholipase A(2) (PLA(2)) is a highly expressed regulator to promote the growth of various cancers and is an ideal target to treat cancers. In this study, a novel strategy based on ligand–receptor interactions to discover novel PLA(2) inhibitors was established, in which PLA(2)-functionalized Fe(3)O(4)@PLGA-PEG-NH(2) magnetic nanoparticles were used as a supporting material combined with high-performance liquid chromatography–mass spectrometry, aiming to accelerate the discovery of novel PLA(2) inhibitors from natural sources such as mangrove endophytic fungi. Under the optimized ligand fishing conditions, six target compounds were ultimately fished and identified to be cyclic peptides (1–3) and sterols (4–6), which compounds 1, 2 and 4–6 have well-documented cytotoxicities. Compound 3 exerted better inhibitory effect on A549 cells by experiment. In conclusion, PLA(2)-functionalized Fe(3)O(4)@PLGA-PEG-NH(2) magnetic nanoparticles-based ligand fishing provided a feasible, selective and effective platform for the efficient screening and identification of antitumor components from natural products.
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spelling pubmed-80697862021-04-26 Rapid Screening and Identification of Antitumor Ingredients from the Mangrove Endophytic Fungus Using an Enzyme-Immobilized Magnetic Nanoparticulate System Wei, Nan Zhao, Jun Wu, Guimei Cao, Wenjuan Luo, Pei Zhang, Zhifeng Chen, Gang Wen, Lu Molecules Article As a consequence of recent progression in biomedicine and nanotechnology, nanoparticle-based systems have evolved as a new method with extensive applications in responsive therapy, multimodal imaging, drug delivery and natural product separation. Meanwhile, the magnetic nanoparticulate system has aroused great interest for separation and purification because of its excellent magnetic properties. Phospholipase A(2) (PLA(2)) is a highly expressed regulator to promote the growth of various cancers and is an ideal target to treat cancers. In this study, a novel strategy based on ligand–receptor interactions to discover novel PLA(2) inhibitors was established, in which PLA(2)-functionalized Fe(3)O(4)@PLGA-PEG-NH(2) magnetic nanoparticles were used as a supporting material combined with high-performance liquid chromatography–mass spectrometry, aiming to accelerate the discovery of novel PLA(2) inhibitors from natural sources such as mangrove endophytic fungi. Under the optimized ligand fishing conditions, six target compounds were ultimately fished and identified to be cyclic peptides (1–3) and sterols (4–6), which compounds 1, 2 and 4–6 have well-documented cytotoxicities. Compound 3 exerted better inhibitory effect on A549 cells by experiment. In conclusion, PLA(2)-functionalized Fe(3)O(4)@PLGA-PEG-NH(2) magnetic nanoparticles-based ligand fishing provided a feasible, selective and effective platform for the efficient screening and identification of antitumor components from natural products. MDPI 2021-04-13 /pmc/articles/PMC8069786/ /pubmed/33924693 http://dx.doi.org/10.3390/molecules26082255 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wei, Nan
Zhao, Jun
Wu, Guimei
Cao, Wenjuan
Luo, Pei
Zhang, Zhifeng
Chen, Gang
Wen, Lu
Rapid Screening and Identification of Antitumor Ingredients from the Mangrove Endophytic Fungus Using an Enzyme-Immobilized Magnetic Nanoparticulate System
title Rapid Screening and Identification of Antitumor Ingredients from the Mangrove Endophytic Fungus Using an Enzyme-Immobilized Magnetic Nanoparticulate System
title_full Rapid Screening and Identification of Antitumor Ingredients from the Mangrove Endophytic Fungus Using an Enzyme-Immobilized Magnetic Nanoparticulate System
title_fullStr Rapid Screening and Identification of Antitumor Ingredients from the Mangrove Endophytic Fungus Using an Enzyme-Immobilized Magnetic Nanoparticulate System
title_full_unstemmed Rapid Screening and Identification of Antitumor Ingredients from the Mangrove Endophytic Fungus Using an Enzyme-Immobilized Magnetic Nanoparticulate System
title_short Rapid Screening and Identification of Antitumor Ingredients from the Mangrove Endophytic Fungus Using an Enzyme-Immobilized Magnetic Nanoparticulate System
title_sort rapid screening and identification of antitumor ingredients from the mangrove endophytic fungus using an enzyme-immobilized magnetic nanoparticulate system
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8069786/
https://www.ncbi.nlm.nih.gov/pubmed/33924693
http://dx.doi.org/10.3390/molecules26082255
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