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一种颜色可调的多功能生物发光探针。

A versatile bioluminescent probe with tunable color.

作者信息

Torrey Zachary R, Halbers Lila P, Scipioni Lorenzo, Tedeschi Giulia, Digman Michelle A, Prescher Jennifer A

机构信息

Department of Chemistry, University of California Irvine Irvine CA 92697 USA

Department of Pharmaceutical Sciences, University of California Irvine Irvine CA 92697 USA.

出版信息

RSC Chem Biol. 2024 Sep 20;5(11):1097-103. doi: 10.1039/d4cb00101j.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e67/11523296/9097a1e8d1dd/d4cb00101j-f1.jpg

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