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Enabling the Triplet of Tetraphenylethene to Sensitize the Excited State of Europium(III) for Protein Detection and Time‐Resolved Luminescence Imaging

机译:使四苯乙烯的三重态能够激发Euro(III)的激发态用于蛋白质检测和时间分辨发光成像

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摘要

A tetraphenylethene (TPE) group that exhibits aggregation‐induced emission is incorporated into the ligand of a Eu(III) complex (TPEEu) to sensitize the excited state of Eu(III). In steady‐state measurements, TPEEu exhibits weak luminescence when dissolved in aqueous solutions even at a high concentration level, but emits strong fluorescence of TPE and phosphorescence of Eu(III) upon binding with bovine serum albumin. With a delay time of 0.05 ms and a gate time of 1.0 ms in time‐resolved measurements, only phosphorescent emission of Eu(III) is observed with a high on/off ratio. Moreover, this probe is successfully used in time‐resolved luminescence imaging to eliminate the background signal from biological autofluorescence without a washing process. This work provides a general strategy in designing Ln(III) complexes for detecting a broad range of biological molecules.
机译:表现出聚集诱导发射的四苯基乙烯(TPE)基团被掺入Eu(III)配合物(TPEEu)的配体中,以激发Eu(III)的激发态。在稳态测量中,即使在高浓度下,TPEEu溶于水溶液时仍显示弱发光,但与牛血清白蛋白结合后,TPEEu发出强的TPE荧光和Eu(III)的磷光。在时间分辨的测量中,延迟时间为0.05毫秒,选通时间为1.0毫秒,仅观察到高开/关比的Eu(III)磷光发射。此外,该探针已成功用于时间分辨发光成像中,无需清洗即可消除生物自发荧光的背景信号。这项工作提供了设计Ln(III)配合物以检测广泛的生物分子的一般策略。

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