Torrey Zachary R, Halbers Lila P, Scipioni Lorenzo, Tedeschi Giulia, Digman Michelle A, Prescher Jennifer A
Department of Chemistry, University of California Irvine Irvine CA 92697 USA
Department of Pharmaceutical Sciences, University of California Irvine Irvine CA 92697 USA.
RSC Chem Biol. 2024 Sep 20;5(11):1097-103. doi: 10.1039/d4cb00101j.
Bioluminescence is a powerful method for imaging , but applications at the microscale are far from routine. This is due, in part, to a lack of versatile tools for visualizing dynamic events. To address this void, we developed a new platform-Bioluminescence Resonance Energy mAKe over with a Fluorescence-Activating absorption-Shifting Tag (BREAKFAST). BREAKFAST features a bright luciferase combined with a chemogenetic tag (pFAST) for rapid color switching. In the presence of luciferin and a discrete fluorogenic ligand, signal is observed resonance energy transfer. We evaluated spectral outputs with various fluorogens and established the utility of BREAKFAST for combined fluorescence and bioluminescence imaging. Dynamic, four-color visualization was achieved with sequential ligand addition and spectral phasor analysis. We further showed selective signal quenching with a dark fluorogen. Collectively, this work establishes a new method for bioluminescence imaging at the cellular scale and sets the stage for continued probe development.
生物发光是一种强大的成像方法,但在微观尺度上的应用远未成为常规操作。部分原因在于缺乏用于可视化动态事件的通用工具。为填补这一空白,我们开发了一个新平台——生物发光共振能量转换荧光激活吸收位移标签(BREAKFAST)。BREAKFAST的特点是一种明亮的荧光素酶与一个化学遗传标签(pFAST)相结合,用于快速颜色切换。在荧光素和一种离散的荧光配体存在的情况下,通过共振能量转移观察到信号。我们用各种荧光团评估了光谱输出,并确立了BREAKFAST在荧光和生物发光联合成像方面的实用性。通过顺序添加配体和光谱相量分析实现了动态四色可视化。我们进一步展示了使用一种暗荧光团进行选择性信号淬灭。总体而言,这项工作建立了一种在细胞尺度上进行生物发光成像的新方法,并为持续的探针开发奠定了基础。