Yang Bin, Tian Ruowei, Guo Taiyu, Qu Wangbo, Lu Jiao, Li Yong, Wu Zhou, Yan Shihai, Geng Zhirong, Wang Zhilin
State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Collaborative Innovation Center of Advanced Microstructures, Nanjing University, Nanjing 210023, P. R. China.
College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210046, P. R. China.
Anal Chem. 2023 Mar 21;95(11):5034-5044. doi: 10.1021/acs.analchem.2c05523. Epub 2023 Mar 10.
Adenosine triphosphate (ATP), as an important intracellular energy currency produced in mitochondria, is closely related to various diseases in living organisms. Currently, the biological application of AIE fluorophore as a fluorescent probe for ATP detection in mitochondria is rarely reported. Herein, D-π-A and D-A structure-based tetraphenylethylene (TPE) fluorophores were employed to synthesize six different ATP probes (P1-P6), and the phenylboronic acid groups and dual positive charge sites of probes could interact with the vicinal diol of ribose and negatively charged triphosphate structure of ATP, respectively. However, P1 and P4 with a boronic acid group and a positive charge site had poor selectivity for ATP detection. In contrast, P2, P3, P5, and P6 with dual positive charge sites exhibited better selectivity than P1 and P4. In particular, P2 had more advantages of high sensitivity, selectivity, and good time stability for ATP detection than P3, P5, and P6, which was ascribed to its D-π-A structure, linker 1 (1,4-bis(bromomethyl)benzene), and dual positive charge recognition sites. Then, P2 was employed to detect ATP, and it exhibited a low detection limit of 3.62 μM. Moreover, P2 showed utility in the monitoring of mitochondrial ATP level fluctuations.
三磷酸腺苷(ATP)作为线粒体中产生的一种重要的细胞内能量货币,与生物体中的各种疾病密切相关。目前,关于聚集诱导发光(AIE)荧光团作为线粒体中ATP检测荧光探针的生物学应用鲜有报道。在此,基于D-π-A和D-A结构的四苯乙烯(TPE)荧光团被用于合成六种不同的ATP探针(P1-P6),探针的苯基硼酸基团和双正电荷位点可分别与核糖的邻二醇和ATP带负电荷的三磷酸结构相互作用。然而,具有硼酸基团和一个正电荷位点的P1和P4对ATP检测的选择性较差。相比之下,具有双正电荷位点的P2、P3、P5和P6表现出比P1和P4更好的选择性。特别是,P2在ATP检测方面比P3、P5和P6具有更高的灵敏度、选择性和良好的时间稳定性等更多优势,这归因于其D-π-A结构、连接基1(1,4-双(溴甲基)苯)和双正电荷识别位点。然后,使用P2检测ATP,其检测限低至3.62μM。此外,P2在监测线粒体ATP水平波动方面显示出实用性。