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Enzyme-free ultrasensitive fluorescence detection of epithelial cell adhesion molecules based on a toehold-aided DNA recycling amplification strategy

机译:基于脚趾辅助DNA回收扩增策略的无酶超敏荧光检测上皮细胞粘附分子

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Epithelial cell adhesion molecules (EpCAMs) play a significant role in tumorigenesis and tumor development. EpCAMs are considered to be tumor signaling molecules for cancer diagnosis, prognosis and therapy. Herein, an enzyme-free and highly sensitive fluorescent biosensor, with a combined aptamer-based EpCAM recognition and toehold-aided DNA recycling amplification strategy, was developed for sensitive and specific fluorescence detection of EpCAMs. Due to highly specific binding between EpCAMs and corresponding aptamers, strand a, which is released from the complex of aptamer/strand a in the presence of EpCAMs which is bound to the corresponding aptamer, triggered the toehold-mediated strand displacement process. An amplified fluorescent signal was achieved by recycling strand a for ultrasensitive EpCAM detection with a detection limit as low as 0.1 ng mL ~(?1) , which was comparable or superior to that of reported immunoassays and biosensor strategies. In addition, high selectivity towards EpCAMs was exhibited when other proteins were selected as control proteins. Finally, this strategy was successfully used for the ultrasensitive fluorescence detection of EpCAMs in human serum samples with satisfactory results. Importantly, the present strategy may be also expanded for the detection of other targets using the corresponding aptamers.
机译:上皮细胞粘附分子(EpCAM)在肿瘤发生和肿瘤发展中起重要作用。 EpCAM被认为是用于癌症诊断,预后和治疗的肿瘤信号分子。在本文中,开发了一种无酶,高灵敏度的荧光生物传感器,结合了基于适体的EpCAM识别和脚趾辅助DNA回收扩增策略,用于EpCAM的灵敏和特异性荧光检测。由于EpCAM和相应的适体之间的高度特异性结合,在与相应的适体结合的EpCAM的存在下,从适体/链α的复合物中释放的链a触发了脚趾介导的链置换过程。通过回收链a用于超灵敏的EpCAM检测,可实现放大的荧光信号,其检测限低至0.1 ng mL〜(?1),与已报道的免疫测定和生物传感器策略相当或更好。另外,当其它蛋白作为对照蛋白展出朝EpCAMs高选择性。最终,该策略成功用于人血清样品中EpCAM的超灵敏荧光检测,结果令人满意。重要的是,本策略也可以扩展为使用相应的适体来检测其他靶标。

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