State Key Laboratory of Marine Resource Utilization in South China Sea, Hainan University, Haikou, 570228, P. R. China.
Angew Chem Int Ed Engl. 2022 Mar 1;61(10):e202115886. doi: 10.1002/anie.202115886. Epub 2022 Jan 17.
The detection of environmental uranyl is attracting increasing attention. However, the available detection strategies mainly depend on the selective recognition of uranyl, which is subject to severe interference by coexisting metal ions. Herein, based on the unique uranyl-triggered photocleavage property, the protein BSA is labelled with fluorescent molecules that exhibit an aggregation-induced emission effect for uranyl detection. Uranyl-triggered photocleavage causes the separation of the fluorescent-molecule-labelled protein fragments, leading to attenuation of the emission fluorescence, which is used as a signal for uranyl detection. This detection strategy shows high selectivity for uranyl and an ultralow detection limit of 24 pM with a broad detection range covering five orders of magnitude. The detection method also shows high reliability and stability, making it a promising technique for practical applications in diverse environments.
环境中铀酰的检测正引起越来越多的关注。然而,现有的检测策略主要依赖于铀酰的选择性识别,这受到共存金属离子的严重干扰。在此,基于铀酰所引发的独特光解特性,用具有聚集诱导发射效应的荧光分子对牛血清白蛋白(BSA)进行标记,用于铀酰的检测。铀酰所引发的光解会导致荧光分子标记的蛋白质片段分离,从而减弱发射荧光,这可作为铀酰检测的信号。该检测策略对铀酰表现出高选择性,检测下限低至 24 pM,检测范围涵盖五个数量级。该检测方法还表现出高可靠性和稳定性,有望在各种环境中得到实际应用。