Department of Neurobiology, Stanford University, Stanford, CA, USA.
Department of Bioengineering, Stanford University, Stanford, CA, USA.
Nat Methods. 2020 Aug;17(8):852-860. doi: 10.1038/s41592-020-0889-6. Epub 2020 Jul 13.
Sensitive detection of two biological events in vivo has long been a goal in bioluminescence imaging. Antares, a fusion of the luciferase NanoLuc to the orange fluorescent protein CyOFP, has emerged as a bright bioluminescent reporter with orthogonal substrate specificity to firefly luciferase (FLuc) and its derivatives such as AkaLuc. However, the brightness of Antares in mice is limited by the poor solubility and bioavailability of the NanoLuc substrate furimazine. Here, we report a new substrate, hydrofurimazine, whose enhanced aqueous solubility allows delivery of higher doses to mice. In the liver, Antares with hydrofurimazine exhibited similar brightness to AkaLuc with its substrate AkaLumine. Further chemical exploration generated a second substrate, fluorofurimazine, with even higher brightness in vivo. We used Antares with fluorofurimazine to track tumor size and AkaLuc with AkaLumine to visualize CAR-T cells within the same mice, demonstrating the ability to perform two-population imaging with these two luciferase systems.
在体敏感检测两个生物事件一直是生物发光成像的目标。安塔雷斯(Antares)是荧光素酶 NanoLuc 与橙色荧光蛋白 CyOFP 的融合体,作为一种明亮的生物发光报告蛋白,它具有与萤火虫荧光素酶(FLuc)及其衍生物(如 AkaLuc)正交的底物特异性。然而,安塔雷斯在小鼠中的亮度受到 NanoLuc 底物 furimazine 较差的溶解度和生物利用度的限制。在这里,我们报告了一种新的底物,即羟 furimazine,其增强的水溶性允许向小鼠给予更高剂量。在肝脏中,使用羟 furimazine 的 Antares 与使用其底物 AkaLumine 的 AkaLuc 具有相似的亮度。进一步的化学探索生成了第二种底物,氟 furimazine,其在体内的亮度更高。我们使用氟 furimazine 的 Antares 来跟踪肿瘤大小,并用 AkaLumine 的 AkaLuc 可视化小鼠体内的 CAR-T 细胞,证明了这两种荧光素酶系统进行两群体成像的能力。