生物发光
化学
检出限
荧光
发光
分析物
自体荧光
费斯特共振能量转移
部分
光化学
注意事项
分析化学(期刊)
组合化学
光电子学
色谱法
光学
立体化学
生物化学
医学
物理
护理部
作者
Junbin Li,Na Wang,Mengyi Xiong,Min Dai,Cheng Xie,Qianqian Wang,Ke Quan,Yibo Zhou,Zhihe Qing
标识
DOI:10.1021/acs.analchem.2c05422
摘要
Fluorescent probes have emerged as powerful tools for the detection of different analytes by virtue of structural tenability. However, the requirement of an excitation source largely hinders their applicability in point-of-care detection, as well as causing autofluorescence interference in complex samples. Herein, based on bioluminescence resonance energy transfer (BRET), we developed a reaction-based ratiometric bioluminescent platform, which allows the excitation-free detection of analytes. The platform has a modular design consisting of a NanoLuc-HaloTag fusion as an energy donor, to which a synthetic fluorescent probe is bioorthogonally labeled as recognition moiety and energy acceptor. Once activated by the target, the fluorescent probe can be excited by NanoLuc to generate a remarkable BRET signal, resulting in obvious color changes of luminescence, which can be easily recorded and quantitatively analyzed by a smartphone. As a proof of concept, a fluorescent probe for HOCl was synthesized to construct the bioluminescent system. Results demonstrated the system showed a constant blue/red emission ratio which is independent to the signal intensity, allowing the quantification of HOCl concentration with high sensitivity (limit of detection (LOD) = 13 nM) and accuracy. Given the universality, this reaction-based bioluminescent platform holds great potential for point-of-care and quantitative detection of reactive species.
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