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一种用于选择性和时间分辨检测二磷酸腺苷(ADP)的开启型铕(III)发光探针。

A switch-on luminescent europium(iii) probe for selective and time-resolved detection of adenosine diphosphate (ADP).

作者信息

Bodman Samantha E, Stachelek Patrycja, Rehman Umatur, Plasser Felix, Pal Robert, Butler Stephen J

机构信息

Department of Chemistry, Loughborough University Epinal Way Loughborough LE113TU UK

Department of Chemistry, Durham University Durham DH1 3LE UK.

出版信息

Chem Sci. 2025 Feb 19;16(13):5602-5612. doi: 10.1039/d4sc07188c. eCollection 2025 Mar 26.

DOI:10.1039/d4sc07188c
PMID:40028620
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11868914/
Abstract

Adenosine diphosphate (ADP) is a key product of two essential classes of biological reactions, catalysed by ATPases and kinases. This makes ADP a highly appealing target for supramolecular detection. However, doing so selectively is exceedingly difficult due to ADP's lower overall charge and similar structure to ATP and the need for compatibility with biological media. Overcoming this challenge, here we present a water-soluble, ADP-selective, luminescent europium(iii) probe suitable for use and in cellular microscopy. This negatively charged Eu(iii) complex binds ADP reversibly and responds by switching on its luminescence, whilst showing minimal interference from ATP, pyrophosphate and a wide range of biological anions. The probe is equipped with two π-conjugated quinolyl-phenoxyacetate antennae, facilitating excitation at 355 nm in fluorescence microscopy. The ancillary carboxylate groups ensure high water solubility and suppress non-specific binding to albumin protein. Our novel probe demonstrates a level of sensing selectivity for ADP that is unrivaled, producing a linear emission response across the physiologically relevant concentration range (10-400 μM), even in the presence of excess millimolar ATP. We demonstrate that this amphiphilic Eu(iii) probe permeates mammalian cells and localises within the mitochondria and lysosomes. The low background emission of the probe combined with its excellent ADP selectivity and long-lived luminescence makes it a promising tool for visualising ADP levels in living cells.

摘要

二磷酸腺苷(ADP)是由ATP酶和激酶催化的两类重要生物反应的关键产物。这使得ADP成为超分子检测极具吸引力的目标。然而,由于ADP的总电荷较低且结构与ATP相似,以及需要与生物介质兼容,选择性地检测ADP极其困难。为克服这一挑战,我们在此展示一种水溶性、对ADP具有选择性的发光铕(III)探针,适用于细胞显微镜检测。这种带负电荷的铕(III)配合物与ADP可逆结合,并通过开启其发光做出响应,同时对ATP、焦磷酸和多种生物阴离子的干扰极小。该探针配备了两个π共轭喹啉基 - 苯氧基乙酸天线,便于在荧光显微镜下于355 nm处激发。辅助羧基确保了高水溶性并抑制与白蛋白的非特异性结合。我们的新型探针展示出对ADP无与伦比的传感选择性水平,即使在存在过量毫摩尔ATP的情况下,在生理相关浓度范围(10 - 400 μM)内也能产生线性发射响应。我们证明这种两亲性铕(III)探针可渗透哺乳动物细胞并定位于线粒体和溶酶体内。该探针的低背景发射、出色的ADP选择性和长寿命发光使其成为可视化活细胞中ADP水平的有前景的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9b/11938833/817ebd5f6622/d4sc07188c-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9b/11938833/859e89729fbf/d4sc07188c-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9b/11938833/3293677f2e5d/d4sc07188c-s1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9b/11938833/05cf5668622b/d4sc07188c-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9b/11938833/f7e18dc974fc/d4sc07188c-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9b/11938833/e4933cf7d0f4/d4sc07188c-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9b/11938833/d2e58577558b/d4sc07188c-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9b/11938833/a2cdef30f521/d4sc07188c-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9b/11938833/817ebd5f6622/d4sc07188c-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9b/11938833/859e89729fbf/d4sc07188c-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9b/11938833/3293677f2e5d/d4sc07188c-s1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9b/11938833/05cf5668622b/d4sc07188c-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9b/11938833/f7e18dc974fc/d4sc07188c-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9b/11938833/e4933cf7d0f4/d4sc07188c-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9b/11938833/d2e58577558b/d4sc07188c-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9b/11938833/a2cdef30f521/d4sc07188c-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9b/11938833/817ebd5f6622/d4sc07188c-f7.jpg

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