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Fluorometric Detection of Streptavidin with a Cationic Conjugated Polymer and Hairpin DNA Probe

机译:用阳离子共轭聚合物和发夹DNA探针对链霉亲和素的荧光测定学检测

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摘要

A simple and rapid method for streptavidin (SA) detection is developed based on a cationic conjugated polymer (CCP)-mediated fluorescence resonance energy transfer (FRET) between poly [(9,9-bis(6'-N, N, N-trimethylammonium) hexyl) fluorenylene phenylene (PFP) and SYBR Green I (SG I). A hairpin DNA labeled with biotin at the 3' terminus was designed for the binding of SA and SYBR Green I (SG I) so that an amplified signal of emission fluorescence was detected as the CCP-mediated FRET was induced in the presence of SA. The calibration curve exhibited a linear correlation between fluorescence intensity and SA concentration from 0 to 40 nM, and the linear regression equation was y = 0.0467x + 0.5814, with a correlation coefficient (R~2) of 0.9927, and the detection limit was 0.5 nM. Further investigations showed that the method exhibited a significantly high specificity for the target protein and a satisfactory practical performance when human serum samples spiked with SA were tested. The results suggest that this strategy is practically applicable as it may enable an effective tool for studies on the ligand-protein interactions as well as the qualitative and quantitative detection of proteins.
机译:基于阳离子共轭聚合物(CCP)介导的荧光共振能量转移(FRET),开发了一种简单而快速的方法(SA)检测,开发三甲基铵)己基)氟苯基(PFP)和SYBR绿色I(SG I)。设计用于SA和SYBR绿色I(SG I)的3'末端标记的发夹DNA,因此在SA存在下诱导了CCP介导的FRET,从而检测到发射荧光的放大信号。校准曲线在0到40 nm之间表现出荧光强度和SA浓度之间的线性相关性,线性回归方程为y = 0.0467x + 0.5814,相关系数(r〜2)为0.9927,检测极限为0.5 nm。进一步的研究表明,该方法对靶蛋白的特异性显着高,并且当测试了与SA尖叫的人血清样品时的实践表现。结果表明,该策略实际上是适用的,因为它可以为研究配体 - 蛋白质相互作用以及蛋白质的定性和定量检测提供有效的工具。

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