Time-resolved fluorescence technique can reduce the short-lived background luminescence and auto-fluorescence interference from cells and tissues by exerting the delay time between pulsed excitation light and signal acquisition. Here, we prepared persistent luminescence nanoparticles (PLNPs) to design a universal time-resolved fluorescence resonance energy transfer (TR-FRET) platform for biosensing, lifetime imaging of cell apoptosis and in situ lifetime quantification of intracellular caspase-3. Three kinds of PLNPs-based nanoprobes are assembled by covalently binding dye-labeled peptides or DNA to carboxyl-functionalized PLNPs for the efficient detection of caspase-3, microRNA and protein. The peptides-functionalized nanoprobe is also employed for fluorescence lifetime imaging to monitor cell apoptosis, which shows a dependence of cellular fluorescence lifetime on caspase-3 activity and thus leads to an in situ quantification method. This work provides a proof-of-concept for PLNPs-based TR-FRET analysis and demonstrates its potential in exploring dynamical information of life process.

译文

时间分辨荧光技术可以通过在脉冲激发光和信号采集之间施加延迟时间来减少来自细胞和组织的短寿命背景发光和自荧光干扰。在这里,我们制备了持久性发光纳米颗粒 (PLNPs),以设计通用的时间分辨荧光共振能量转移 (tr-fret) 平台,用于生物传感,细胞凋亡的寿命成像和细胞内caspase-3的原位寿命定量。通过将染料标记的肽或DNA与羧基官能化的plnp共价结合来组装三种基于plnp的纳米探针,以有效检测caspase-3,microRNA和蛋白质。肽官能化的纳米探针也用于荧光寿命成像以监测细胞凋亡,这显示了细胞荧光寿命对caspase-3活性的依赖性,因此导致了原位定量方法。这项工作为基于PLNPs的TR-FRET分析提供了概念验证,并证明了其在探索生命过程的动态信息方面的潜力。

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