Department of Chemistry and Biochemistry, 251 Nieuwland Science Hall, University of Notre Dame, IN 46556, USA.
Org Biomol Chem. 2021 May 12;19(18):4100-4106. doi: 10.1039/d1ob00426c.
Continued advancement in bioresponsive fluorescence imaging requires new classes of activatable fluorescent probes that emit near-infrared fluorescence with wavelengths above 740 nm. Heptamethine cyanine dyes (Cy7) have suitable fluorescence properties but it is challenging to create activatable probes because Cy7 dyes have a propensity for self-aggregation and fluorescence quenching. A new synthetic strategy is employed to create a generalizable class of hydrophilic bioresponsive near-infrared fluorescent probes with appended sulfonates that provide excellent physiochemical properties. A prototype version is triggered by nitroreductase enzyme to undergo self-immolative cleavage with a large enhancement in fluorescence signal at 780 nm and the probe enables microscopic imaging of cell hypoxia with "turn on" fluorescence. Near-infrared fluorescence imaging of hypoxia is potentially useful in many different areas of biomedical research and clinical treatment.
持续推进的生物响应荧光成像需要新型的可激活荧光探针,这些探针发射的近红外荧光波长在 740nm 以上。庚甲川染料(Cy7)具有合适的荧光性质,但由于 Cy7 染料有自聚集和荧光猝灭的倾向,因此很难创建可激活的探针。本研究采用了一种新的合成策略,创建了一类带有磺酸基的可水解析出的生物响应近红外荧光探针,具有优异的理化性质。原型探针可被硝基还原酶触发,通过自耗性断裂,在 780nm 处产生荧光信号的大幅增强,该探针可实现细胞缺氧的微观成像,呈现出“开启”的荧光。近红外荧光成像技术在生物医学研究和临床治疗的许多不同领域都有潜在的应用价值。