Department of Chemistry and Nanoscience, Ewha Womans University, Seoul 03760, Korea.
Beijing National Laboratory for Molecular Sciences, Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
Chem Soc Rev. 2022 Jan 24;51(2):450-463. doi: 10.1039/d1cs00543j.
As the main biomarkers of most diseases, enzymes play fundamental but extremely critical roles in biosystems. High-resolution studies of enzymes using activatable fluorescence imaging may help to better elucidate their dynamics in living systems. Currently, most activatable probes can realize changeable imaging of enzymes but inevitably tend to diffuse away from the original active site of the enzyme and even translocate out of cells, seriously impairing high-resolution observation of the enzymes. fluorescence imaging of enzymes can be realized by labelling probes or antibodies with always-on signals that fail to enable activatable imaging of enzymes. Thus, fluorescent probes with both "activatable" and "" properties will enable high-resolution studies of enzymes in living systems. In this tutorial review, we summarize the existing methods ranging from design strategies to bioimaging applications that could be used to develop activatable fluorescent probes for imaging of enzymes. It is expected that this tutorial review will promote the new methods generated to design such probes for better deciphering enzymes in complex biosystems and further extend the application of these methods to other fields of enzymes.
作为大多数疾病的主要生物标志物,酶在生物系统中起着至关重要但又极其关键的作用。使用可激活荧光成像技术对酶进行高分辨率研究,可能有助于更好地阐明它们在活系统中的动态。目前,大多数可激活探针可以实现对酶的可变成像,但不可避免地会从酶的原始活性部位扩散出去,甚至发生细胞易位,严重损害对酶的高分辨率观察。通过用常闭信号标记探针或抗体对酶进行荧光成像,无法实现酶的可激活成像。因此,具有“可激活”和“常闭”双重特性的荧光探针将能够在活系统中对酶进行高分辨率研究。在本综述中,我们总结了现有的从设计策略到生物成像应用的方法,这些方法可用于开发用于酶成像的可激活荧光探针。我们期望本综述将促进新方法的产生,以设计此类探针,从而更好地破译复杂生物系统中的酶,并将这些方法进一步扩展到酶的其他领域。