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基于 InP/ZnS 量子点嵌入介孔纳米粒子的荧光配体捕捞结合原位成像与表征筛选姜黄中 HSP90 抑制剂。

Fluorescent ligand fishing combination with in-situ imaging and characterizing to screen Hsp 90 inhibitors from Curcuma longa L. based on InP/ZnS quantum dots embedded mesoporous nanoparticles.

机构信息

School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, 210023, China.

Jiangsu Key Laboratory of Pediatric Respiratory Disease, Nanjing 210023, China.

出版信息

Talanta. 2018 Feb 1;178:258-267. doi: 10.1016/j.talanta.2017.09.035. Epub 2017 Sep 15.

DOI:10.1016/j.talanta.2017.09.035
PMID:29136820
Abstract

Although ligand fishing has been shown to be an efficient technique for the identification of bioactive components from complex mixtures such as natural products, it cannot be applied to biomedical image processing. Herein, a specific fluorescent ligand fishing combined with in situ imaging approach is presented for the identification of heat shock protein 90 (Hsp 90) inhibitors from complex matrixes, Curcuma longa L., using N-terminus immobilized Hsp 90α functionalized InP/ZnS quantum dots embedded mesoporous nanoparticles (i.e. Hsp 90α (NT)-FQDNs) as extraction sorbents and fluorescent tracer. The fished ligands were identified by liquid chromatography time-of-flight/mass spectrometry (LC-TOF/MS) and gas chromatography-mass spectrometry (GC-MS). Moreover, in situ imaging by confocal laser scanning microscopy (CLSM) was applied for evaluating the effect of fished-ligands on bioactivity-induced apoptosis morphologically in HeLa cells. MTT assay verified the bioactivity of the ligands and molecular docking results further provided convincing information to verify the feasible binding mode between ligands and protein. Twelve ligands as potential Hsp 90 inhibitors were ultimately fished and identified from Curcuma longa L. crude extracts. The proposed approach based on Hsp 90α functionalized nanocomposites is superior in the combination of highly specific screening efficiency and concurrent visual in situ imaging, which could have great promise for the development of other plant-derived Hsp 90 inhibitors, and providing a rapid and reliable platform for discovering biologically active molecules in natural products.

摘要

尽管配体捕捞已被证明是从复杂混合物(如天然产物)中鉴定生物活性成分的有效技术,但它不能应用于生物医学图像处理。在此,提出了一种特定的荧光配体捕捞方法,结合原位成像方法,用于从复杂基质姜黄中鉴定热休克蛋白 90(Hsp 90)抑制剂,使用固定在 N 端的 Hsp 90α功能化的 InP/ZnS 量子点嵌入介孔纳米粒子(即 Hsp 90α(NT)-FQDNs)作为提取吸附剂和荧光示踪剂。通过液相色谱飞行时间/质谱(LC-TOF/MS)和气相色谱-质谱(GC-MS)鉴定捕捞到的配体。此外,通过共聚焦激光扫描显微镜(CLSM)进行原位成像,用于评估捕捞配体对 HeLa 细胞中生物活性诱导的细胞凋亡形态的影响。MTT 测定验证了配体的生物活性,分子对接结果进一步提供了令人信服的信息,以验证配体与蛋白质之间可行的结合模式。从姜黄粗提物中最终捕捞和鉴定出 12 种潜在的 Hsp 90 抑制剂。基于 Hsp 90α 功能化纳米复合材料的方法在高特异性筛选效率和同时进行的原位可视化方面具有优势,这对于开发其他植物来源的 Hsp 90 抑制剂具有很大的潜力,并为在天然产物中发现具有生物活性的分子提供了一个快速可靠的平台。

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