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A sensitive fluorescence “turn-off-on” biosensor for poly(ADP-ribose) polymerase-1 detection based on cationic conjugated polymer-MnO2 nanosheets
Sensors and Actuators B: Chemical ( IF 8.0 ) Pub Date : 2018-07-04 , DOI: 10.1016/j.snb.2018.07.013
Shuangshuang Wu , Changhui Chen , Haitang Yang , Wei Wei , Min Wei , Yuanjian Zhang , Songqin Liu

Poly(ADP-ribose) polymerase-1 (PARP-1) monitoring has attracted extensive attention because it serves a vital role in human pathologies. However, only a few researches about its detection methods have been reported because PARP-1 and its catalyzed product poly(ADP-ribose) polymer (PAR) are lack of optical or electrochemical activity. Herein, a convenient fluorescence “turn-off-on” nanosensor based on cationic conjugated polymer (PFP) and MnO2 nanosheets has been designed for selective detection of PARP-1 in vitro. To the best of our knowledge, it is the first time to use manganese dioxide (MnO2) nanosheets for PARP-1 detection. The fluorescence intensity of PFP can be quenched by MnO2 nanosheets via a fluorescence resonance energy transfer (FRET). While the subsequently joined electronegative poly(ADP-ribose) polymer (PAR), catalysate of PARP-1, take positively charged MnO2 nanosheets away from PFP via electrostatic interaction, causing sufficient recovery of fluorescent signal. The sensing platform displayed a sensitive response to PARP-1 in a linear range of 0.03 − 1.5 U (0.024 − 1.2 nM), with a detection limit of 0.004 U (0.003 nM), which is 10–100 lower than reported methods. As expected, this method was successfully applied to the detection of PARP-1 in human serum samples with recoveries ranging from 97.6 − 102.7%. Especially, it has also been applied to the determination of PARP-1 in human breast cancer cells SK-BR-3 in the 40 to 1000 cells per mL range, with a detection limit as low as 25 cells per mL.



中文翻译:

基于阳离子共轭聚合物-MnO 2纳米片的用于ADP-核糖聚合酶-1检测的灵敏荧光“关闭”生物传感器

聚(ADP-核糖)聚合酶-1(PARP-1)监测已引起广泛关注,因为它在人类病理学中起着至关重要的作用。然而,由于PARP-1及其催化产物聚(ADP-核糖)聚合物(PAR)缺乏光学或电化学活性,因此仅报道了少量有关其检测方法的研究。本文中,已经设计了一种基于阳离子共轭聚合物(PFP)和MnO 2纳米片的方便的荧光“关闭”纳米传感器,用于体外选择性检测PARP-1。据我们所知,这是第一次使用二氧化锰(MnO 2)纳米片进行PARP-1检测。可以用MnO 2猝灭PFP的荧光强度纳米片通过荧光共振能量转移(FRET)。随后加入的带负电的聚(ADP-核糖)聚合物(PAR),PARP-1的催化剂,带正电的MnO 2纳米片通过静电相互作用远离PFP,导致荧光信号充分恢复。传感平台在0.03 − 1.5 U(0.024 − 1.2 nM)的线性范围内显示出对PARP-1的敏感响应,检测限为0.004 U(0.003 nM),比报道的方法低10–100。如预期的那样,该方法已成功应用于人血清样品中PARP-1的检测,回收率为97.6-102.7%。尤其是,它也已用于测定人乳腺癌细胞SK-BR-3中PARP-1的含量,检测范围为每毫升40至1000个细胞,检出限低至每毫升25个细胞。

更新日期:2018-07-04
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