Rapid Multicomponent Bioluminescence Imaging via Substrate Unmixing

• Published in: ACS chemical biology 2021-04, Vol.16 (4), p.682-690
• Main Authors: Rathbun, Colin M, Ionkina, Anastasia A, Yao, Zi, Jones, Krysten A, Porterfield, William B, Prescher, Jennifer A
• Format: Article
• Language: English
• Subjects: Animals; HEK293 Cells; Humans; Luminescent Measurements; Molecular Probes; Substrate Specificity
• ISSN: 1554-8929; 1554-8937
• DOI: 10.1021/acschembio.0c00959

Studies of biological function demand probes that can report on processes in real time and in physiological environments. Bioluminescent tools are uniquely suited for this purpose, as they enable sensitive imaging in cells and tissues. Bioluminescent reporters can also be monitored continuously over time without detriment, as excitation light is not required. Rather, light emission derives from luciferase–luciferin reactions. Several engineered luciferases and luciferins have expanded the scope of bioluminescence imaging in recent years. Multicomponent tracking remains challenging, though, due to a lack of streamlined methods to visualize combinations of bioluminescent reporters. Conventional approaches image one luciferase at a time. Consequently, short-term changes in cell growth or gene expression cannot be easily captured. Here, we report a strategy for rapid, multiplexed imaging with a wide range of luciferases and luciferins. Sequential addition of orthogonal luciferins, followed by substrate unmixing, enabled facile detection of multiple luciferases in vitro and in vivo. Multicomponent imaging in mice was also achieved on the minutes-to-hours time scale.