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基于配体垂钓结合高分辨电喷雾电离四级杆-飞行时间质谱从蛇莓中快速鉴定和分离神经氨酸酶抑制剂

Rapid identification and isolation of neuraminidase inhibitors from mockstrawberry ( Andr.) based on ligand fishing combined with HR-ESI-Q-TOF-MS.

作者信息

Luo Sifan, Guo Linbo, Sheng Caimin, Zhao Yumei, Chen Ling, Li Chufang, Jiang Zhengjin, Tian Haiyan

机构信息

Institute of Traditional Chinese Medicine and Natural Products, College of Pharmacy, Jinan University, Guangzhou 510632, China.

Institute of Pharmaceutical Analysis, College of Pharmacy, Jinan University, Guangzhou 510632, China.

出版信息

Acta Pharm Sin B. 2020 Oct;10(10):1846-1855. doi: 10.1016/j.apsb.2020.04.001. Epub 2020 Apr 18.

Abstract

Neuraminidase inhibitors (NAIs) are the mainstay antiviral drugs against influenza infection. In this study, a ligand fishing protocol was developed to screen NAIs using neuraminidase immobilized magnetic beads (NA-MB). After verifying the feasibility of NA-MB with an artificial mixture including NA inhibitors and non-inhibitors, the developed ligand fishing protocol was applied to screen NAIs from the crude extracts of Andr. Twenty-four NA binding compounds were identified from the normal butanol (-BuOH) extract of as potential NAIs by high-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (HPLC-Q-TOF-MS) assisted with Compound Structure Identification (CSI):FingerID, including 12 ellagitannins, 4 brevifolin derivatives, 3 ellagic acid derivatives, and 4 flavonoids. Among them, 9 compounds were isolated and tested for NA inhibitory activities against NA from , and from oseltamivir sensitive and resistant influenza A virus strains. The results indicate that compound has the NA inhibitory activities in both the oseltamivir sensitive and resistant viral NA, with half maximal inhibitory concentration (IC) values of 197.9 and 125.4 μmol/L, respectively. Moreover, can obviously reduce the replication of oseltamivir sensitive and resistant viruses in Madin-Darby canine kidney (MDCK) cells at the concentrations of 40 and 200 μmol/L.

摘要

神经氨酸酶抑制剂(NAIs)是抗流感感染的主要抗病毒药物。在本研究中,开发了一种配体垂钓方案,使用固定有神经氨酸酶的磁珠(NA-MB)筛选NAIs。在用包含NA抑制剂和非抑制剂的人工混合物验证了NA-MB的可行性之后,将所开发的配体垂钓方案应用于从阴行草粗提物中筛选NAIs。通过高效液相色谱-四极杆飞行时间质谱联用(HPLC-Q-TOF-MS)并借助化合物结构鉴定(CSI):指纹识别,从阴行草正丁醇提取物中鉴定出24种与NA结合的化合物作为潜在的NAIs,其中包括12种鞣花单宁、4种短叶苏木酚衍生物、3种鞣花酸衍生物和4种黄酮类化合物。其中,分离出9种化合物并测试了它们对来自乙型流感病毒以及甲型流感病毒奥司他韦敏感和耐药毒株的NA的抑制活性。结果表明,化合物在奥司他韦敏感和耐药的病毒NA中均具有NA抑制活性,半数最大抑制浓度(IC)值分别为197.9和125.4 μmol/L。此外,在40和200 μmol/L的浓度下,化合物能明显降低奥司他韦敏感和耐药病毒在犬肾传代细胞(MDCK)中的复制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bed/7606179/9edaaf4d42c9/fx1.jpg

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