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Aggregation-Induced Energy Transfer of Conjugated Polymer Materials for ATP Sensing

机译:聚合诱导的共轭聚合物材料的能量转移,用于ATP传感。

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Water-soluble conjugated polymers are attractive fluorescent materials for applications in chemical and biological sensing. The molecular wire effect of such polymers amplifies changes in the fluorescence signal, which can be used for detecting various analytes with high sensitivity. In this work, we report an efficient ratiometric fluorescent probe based on a water-soluble conjugated polymer that showed high sensitivity and selectivity toward adenosine S'-triphosphate (ATP). The macromolecular probe consisted of a polyfluorene backbone doped with 5 mol % 1,4-dithienylbenzothiadiazole (DBT) modified by bis-imidazolium and oligo(ethylene glycol) moieties. Solutions of the polymer emitted purple fluorescence, which changed to red upon addition of ATP molecules. The addition of ATP caused the polymer to aggregate, which enhanced fluorescence resonance energy transfer efficiency from the fluorene segments to DBT units, leading to an increase in red emission. The ratio of the fluorescence at these different wavelengths (I-655/I-423) showed a strong dependence on the ATP concentration. PF-DBT-BIMEG also exhibited high selectivity for ATP sensing over other representative anions and discriminated it from adenosine S'-diphosphate (ADP) and adenosine 5'-monophosphate (AMP). This can be explained by the much stronger electrostatic interactions between the polymer and ATP than the interactions between the polymer and ADP or AMP, as confirmed through molecular dynamics simulations.
机译:水溶性共轭聚合物是用于化学和生物传感的有吸引力的荧光材料。这种聚合物的分子线效应放大了荧光信号的变化,可用于以高灵敏度检测各种分析物。在这项工作中,我们报告了一种基于水溶性共轭聚合物的高效比例荧光探针,该探针显示出对腺苷S'-三磷酸(ATP)的高灵敏度和选择性。该大分子探针由掺杂有5 mol%经双咪唑鎓和低聚(乙二醇)部分改性的1,4-二噻吩基苯并噻二唑(DBT)的聚芴骨架组成。聚合物溶液发出紫色荧光,加入ATP分子后变为红色。 ATP的添加导致聚合物聚集,从而增强了从芴链段到DBT单元的荧光共振能量转移效率,导致红色发射的增加。这些不同波长(I-655 / I-423)的荧光比率显示出对ATP浓度的强烈依赖性。 PF-DBT-BIMEG对ATP的传感也比其他代表性阴离子具有更高的选择性,并将其与S'-二磷酸腺苷(ADP)和5'-单磷酸腺苷(AMP)区别开来。可以通过聚合物与ATP之间的静电相互作用比聚合物与ADP或AMP之间的相互作用强得多来解释这一点,这已经通过分子动力学模拟得到了证实。

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