迈向基于esipt的线粒体探针响应ATP水平的一步

Yonghao Li, Dipendra Dahal, Yi Pang
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引用次数: 0

摘要

合成了一种末端基团为苯并吲哚的激发态分子内质子转移探针(ESIPT),其荧光表现出较大的Stokes位移(Δλ≈250 nm)和良好的荧光量子产率(λem≈715 nm, φfl≈ 0.2)。光谱研究表明该探针还参与了一个小的平衡Ar−OH (λem≈715 nm)↔Ar−O−(λem≈610 nm) + H+,这是由酚质子去质子化引起的。这使得双通道响应成为可能。当用于染色生物细胞时,探针对细胞内线粒体表现出极好的选择性,但在≈600 nm处具有异常强的发射。近红外(NIR)发射只有在细胞ATP产生被抑制时才能观察到。因此,该研究展示了一种独特的基于反应的探针,用于检测胞内细胞器中的ATP。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Step Toward ESIPT-Based Mitochondrial Probe That Responds to ATP Level

A Step Toward ESIPT-Based Mitochondrial Probe That Responds to ATP Level

An excited state intramolecular proton transfer (ESIPT) probe with a benzoindolium terminal group has been synthesized, whose fluorescence shows large Stokes’ shift (Δλ≈ 250 nm) and good fluorescence quantum yield (λem≈ 715 nm, φfl≈ 0.2 in CH2Cl2). Spectroscopic studies suggest that the probe is also involved in a minor equilibrium Ar−OH (λem≈ 715 nm) ↔ Ar−Oem≈ 610 nm) + H+, resulting from deprotonation of phenolic proton. This made it possible for two-channel responses. When being used to stain biological cells, the probe exhibits excellent selectivity toward intracellular mitochondria but gives unusually strong emission from ≈600 nm. Near-infrared (NIR) emission is only observable when cellular ATP production is inhibited. The study thus illustrated a unique reaction-based probe for detecting ATP in the intracellular organelle.

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