Okinaka Momoko, Kawatani Minoru, Fujioka Hiroyoshi, Spratt Spencer John, Ito Hiroki, Misawa Yoshihiro, Otake Reika, Ishikawa Aoi, Kojima Ryosuke, Urano Yasuteru, Ozeki Yasuyuki, Kamiya Mako
Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo 113-0033, Japan.
Laboratory for Chemistry and Life Science, Institute of Integrated Research, Institute of Science Tokyo, Yokohama, Kanagawa 226-8501, Japan.
Anal Chem. 2025 Sep 9;97(35):19057-19065. doi: 10.1021/acs.analchem.5c02231. Epub 2025 Aug 27.
Visualizing specific enzyme activities in living systems is important in biomedical research, and Raman imaging probes are particularly suitable for simultaneous multiplexed detection of plural enzyme activities due to their narrow signal peak widths. Here, we present a molecular design strategy for enzyme-activity-detecting Raman probes based on control of aggregation. The probe itself is soluble and diffusive in aqueous solution due to its hydrophilic substrate moiety, but hydrolysis by the target enzyme affords a hydrophobic product that forms aggregates, thereby increasing the local dye concentration, which in turn results in a stronger Raman signal that enables visualization of the enzyme activity. We validated the molecular design by developing Raman probes targeting aminopeptidase, glycosidase and carboxypeptidase. The vibrational frequency can be shifted by isotope-editing, and the developed probes were successfully applied to visualize the activities of aminopeptidase and glycosidase in live cultured cells and spheroids.
在生物医学研究中,可视化活体细胞系统中的特定酶活性具有重要意义。拉曼成像探针因其信号峰宽度窄,特别适合同时多重检测多种酶活性。在此,我们提出一种基于聚集控制的用于检测酶活性的拉曼探针分子设计策略。由于其亲水性底物部分,探针本身在水溶液中可溶且具有扩散性,但目标酶的水解作用会产生一种形成聚集体的疏水性产物,从而增加局部染料浓度,进而导致更强的拉曼信号,实现酶活性的可视化。我们通过开发针对氨肽酶、糖苷酶和羧肽酶的拉曼探针验证了该分子设计。振动频率可通过同位素编辑进行改变,所开发的探针已成功应用于可视化活体细胞和球体中氨肽酶和糖苷酶的活性。