Shen Hanchen, Du Lidong, Xu Changhuo, Wang Bingzhe, Zhou Qingqing, Ye Ruquan, Kwok Ryan T K, Lam Jacky W Y, Xing Guichuan, Sun Jianwei, Liu Tzu-Ming, Tang Ben Zhong
Department of Chemistry, Hong Kong Branch of Chinese National Engineering Research Center for Tissue Restoration and Reconstruction, Department of Chemical and Biological Engineering, Division of Life Science, and State Key Laboratory of Molecular Neuroscience, The Hong Kong University of Science and Technology, Hong Kong 999077, China.
MOE Frontiers Science Center for Precision Oncology, Faculty of Health Sciences, University of Macau, Macau 999078, China.
ACS Nano. 2024 Jul 26. doi: 10.1021/acsnano.4c03963.
Activity-based detection of γ-Glutamyltranspeptidase (GGT) using near-infrared (NIR) fluorescent probes is a promising strategy for early cancer diagnosis. Although NIR pyridinium probes show high performance in biochemical analysis, the aggregation of both the probes and parental fluorochromes in biological environments is prone to result in a low signal-to-noise ratio (SBR), thus affecting their clinical applications. Here, we develop a GGT-activatable aggregate probe called OTBP-G for two-photon fluorescence imaging in various biological environments under 1040 nm excitation. By rationally tunning the hydrophilicity and donor-acceptor strength, we enable a synergistic effect between twisted intramolecular charge transfer and intersystem crossing processes and realize a perfect dark state for OTBP-G before activation. After the enzymatic reaction, the parental fluorochrome exhibits bright aggregation-induced emission peaking at 670 nm. The fluorochrome-to-probe transformation can induce 1000-fold fluorescence ON/OFF ratio, realizing GGT detection with an SBR > 900. Activation of OTBP-G occurs within 1 min showing an SBR > 400 in mouse ear blood vessels. OTBP-G can further enable the early detection of pulmonary metastasis in breast cancer by topically spraying, outperforming the clinical standard hematoxylin and eosin staining. We anticipate that the in-depth study of OTBP-G can prompt the development of early cancer diagnosis and tumor-related physiological research. Moreover, this work highlights the crucial role of hydrophilicity and donor-acceptor strength in maximizing the ON/OFF ratio of the TICT probes and showcases the potential of OTBP as a versatile platform for activity-based sensing.
使用近红外(NIR)荧光探针基于活性检测γ-谷氨酰转肽酶(GGT)是早期癌症诊断的一种有前景的策略。尽管近红外吡啶鎓探针在生化分析中表现出高性能,但在生物环境中探针和亲本荧光团的聚集容易导致低信噪比(SBR),从而影响其临床应用。在此,我们开发了一种名为OTBP-G的GGT可激活聚集探针,用于在1040nm激发下在各种生物环境中进行双光子荧光成像。通过合理调节亲水性和供体-受体强度,我们实现了扭曲分子内电荷转移和系间窜越过程之间的协同效应,并在激活前为OTBP-G实现了完美的暗态。酶促反应后,亲本荧光团在670nm处呈现明亮的聚集诱导发光峰。荧光团到探针的转变可诱导1000倍的荧光开/关比,实现SBR>900的GGT检测。OTBP-G在1分钟内发生激活,在小鼠耳血管中显示SBR>400。OTBP-G通过局部喷涂可进一步实现乳腺癌肺转移的早期检测,优于临床标准苏木精和伊红染色。我们预计对OTBP-G的深入研究可以促进早期癌症诊断和肿瘤相关生理研究的发展。此外,这项工作突出了亲水性和供体-受体强度在最大化TICT探针开/关比方面的关键作用,并展示了OTBP作为基于活性传感的通用平台的潜力。