Viviani Vadim R, Bevilaqua Vanessa R, de Souza Daniel R, Pelentir Gabriel F, Kakiuchi Michio, Hirano Takashi
Graduate Program of Evolutive Genetics and Molecular Biology, Federal University of São Carlos (UFSCar), 18052-780 São Carlos, São Paulo, Brazil.
Graduate Program of Biotechnology and Environmental Monitoring, Federal University of São Carlos (UFSCar), 18119-001 Sorocaba, São Paulo, Brazil.
Int J Mol Sci. 2020 Dec 30;22(1):303. doi: 10.3390/ijms22010303.
Beetle luciferases produce bioluminescence (BL) colors ranging from green to red, having been extensively used for many bioanalytical purposes, including bioimaging of pathogen infections and metastasis proliferation in living animal models and cell culture. For bioimaging purposes in mammalian tissues, red bioluminescence is preferred, due to the lower self-absorption of light at longer wavelengths by hemoglobin, myoglobin and melanin. Red bioluminescence is naturally produced only by railroad worm luciferase (PxRE), and by some engineered beetle luciferases. However, Far-Red (FR) and Near-Infrared (NIR) bioluminescence is best suited for bioimaging in mammalian tissues due to its higher penetrability. Although some FR and NIR emitting luciferin analogs have been already developed, they usually emit much lower bioluminescence activity when compared to the original luciferin-luciferases. Using site-directed mutagenesis of PxRE luciferase in combination with 6'-modified amino-luciferin analogs, we finally selected novel FR combinations displaying BL ranging from 636-655 nm. Among them, the combination of PxRE-R215K mutant with 6'-(1-pyrrolidinyl)luciferin proved to be the best combination, displaying the highest BL activity with a catalytic efficiency ~2.5 times higher than the combination with native firefly luciferin, producing the second most FR-shifted bioluminescence (650 nm), being several orders of magnitude brighter than commercial with firefly luciferase. Such combination also showed higher thermostability, slower BL decay time and better penetrability across bacterial cell membranes, resulting in ~3 times higher in vivo BL activity in bacterial cells than with firefly luciferin. Overall, this is the brightest FR emitting combination ever reported, and is very promising for bioimaging purposes in mammalian tissues.
甲虫荧光素酶产生的生物发光(BL)颜色范围从绿色到红色,已被广泛用于许多生物分析目的,包括在活体动物模型和细胞培养中对病原体感染和转移增殖进行生物成像。对于哺乳动物组织中的生物成像目的,由于血红蛋白、肌红蛋白和黑色素在较长波长下对光的自吸收较低,红色生物发光是首选。红色生物发光仅由铁路蠕虫荧光素酶(PxRE)和一些工程化甲虫荧光素酶天然产生。然而,远红光(FR)和近红外(NIR)生物发光因其更高的穿透性而最适合用于哺乳动物组织中的生物成像。尽管已经开发了一些发射FR和NIR的荧光素类似物,但与原始荧光素-荧光素酶相比,它们通常发射的生物发光活性要低得多。通过对PxRE荧光素酶进行定点诱变并结合6'-修饰的氨基荧光素类似物,我们最终筛选出了新型FR组合,其生物发光波长范围为636-655nm。其中,PxRE-R215K突变体与6'-(1-吡咯烷基)荧光素的组合被证明是最佳组合,显示出最高的生物发光活性,催化效率比与天然萤火虫荧光素的组合高约2.5倍,产生的生物发光向FR方向移动程度居第二(650nm),比商业萤火虫荧光素酶亮几个数量级。这种组合还表现出更高的热稳定性、更慢的生物发光衰减时间以及更好的跨细菌细胞膜穿透性,导致细菌细胞中的体内生物发光活性比使用萤火虫荧光素时高约3倍。总体而言,这是有史以来报道的最亮的发射FR的组合,在哺乳动物组织的生物成像方面非常有前景。