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利用酶固定化磁性纳米颗粒系统快速筛选和鉴定红树林内生真菌中的抗肿瘤成分。

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

机构信息

School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou 510006, China.

State Key Laboratory for Quality Research in Chinese Medicine, Macau University of Science and Technology, Macau 000853, China.

出版信息

Molecules. 2021 Apr 13;26(8):2255. doi: 10.3390/molecules26082255.

Abstract

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 (PLA) 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 inhibitors was established, in which PLA-functionalized FeO@PLGA-PEG-NH magnetic nanoparticles were used as a supporting material combined with high-performance liquid chromatography-mass spectrometry, aiming to accelerate the discovery of novel PLA 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 (-) and sterols (-), which compounds , and - have well-documented cytotoxicities. Compound exerted better inhibitory effect on A549 cells by experiment. In conclusion, PLA-functionalized FeO@PLGA-PEG-NH magnetic nanoparticles-based ligand fishing provided a feasible, selective and effective platform for the efficient screening and identification of antitumor components from natural products.

摘要

由于生物医学和纳米技术的最新进展,基于纳米粒子的系统已经发展成为一种新方法,在响应性治疗、多模态成像、药物输送和天然产物分离等方面有广泛的应用。同时,由于其优异的磁性能,磁性纳米颗粒系统已引起人们对分离和纯化的极大兴趣。磷脂酶 A (PLA) 是一种高度表达的调节剂,可促进各种癌症的生长,是治疗癌症的理想靶点。在这项研究中,建立了一种基于配体-受体相互作用的新型策略,用于发现新型 PLA 抑制剂,其中 PLA 功能化的 FeO@PLGA-PEG-NH 磁性纳米粒子被用作支撑材料,结合高效液相色谱-质谱法,旨在加速从红树林内生真菌等天然来源中发现新型 PLA 抑制剂。在优化的配体钓取条件下,最终钓取并鉴定了 6 种目标化合物,均为环状肽(-)和甾醇(-),化合物 、 和 - 具有明确的细胞毒性。实验表明,化合物 对 A549 细胞的抑制效果更好。总之,基于 PLA 功能化的 FeO@PLGA-PEG-NH 磁性纳米粒子的配体钓取为从天然产物中高效筛选和鉴定抗肿瘤成分提供了一种可行、选择性和有效的平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07f8/8069786/dca32991d51d/molecules-26-02255-g001.jpg

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