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紫杉醇荧光类似物的合成,该类似物选择性结合微管并灵敏检测 P-糖蛋白外排。

Synthesis of a Fluorescent Analogue of Paclitaxel That Selectively Binds Microtubules and Sensitively Detects Efflux by P-Glycoprotein.

机构信息

Department of Medicinal Chemistry, The University of Kansas, Lawrence, KS, 66045, USA.

出版信息

Angew Chem Int Ed Engl. 2017 Jun 6;56(24):6927-6931. doi: 10.1002/anie.201703298. Epub 2017 May 9.

Abstract

The anticancer drug paclitaxel (Taxol) exhibits paradoxical and poorly understood effects against slow-growing tumors. To investigate its biological activity, fluorophores such as Oregon Green have been linked to this drug. However, this modification increases its polarity by approximately 1000-fold and reduces the toxicity of Taxol towards cancer cell lines by over 200-fold. To construct more drug-like fluorescent probes suitable for imaging by confocal microscopy and analysis by flow cytometry, we synthesized derivatives of Taxol linked to the drug-like fluorophore Pacific Blue (PB). We found that PB-Gly-Taxol bound the target protein β-tubulin with both high affinity in vitro and high specificity in living cells, exhibited substantial cytotoxicity towards HeLa cells, and was a highly sensitive substrate of the multidrug resistance transporter P-glycoprotein (P-gp).

摘要

抗癌药物紫杉醇(Taxol)对生长缓慢的肿瘤表现出矛盾且难以理解的作用。为了研究其生物学活性,已将荧光团(如 Oregon Green)与该药物连接。然而,这种修饰使药物的极性增加了约 1000 倍,使紫杉醇对癌细胞系的毒性降低了 200 多倍。为了构建更适合通过共聚焦显微镜成像和流式细胞术分析的类药物荧光探针,我们合成了与药物样荧光团 Pacific Blue(PB)连接的 Taxol 衍生物。我们发现 PB-Gly-Taxol 在体外与靶蛋白β-微管蛋白具有高亲和力和高特异性结合,对 HeLa 细胞表现出显著的细胞毒性,并且是多药耐药转运蛋白 P-糖蛋白(P-gp)的高度敏感底物。

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