4.7 Article

A unified fluorescence quenching mechanism of tetrazine-based fluorogenic dyes: energy transfer to a dark state

Journal

MATERIALS CHEMISTRY FRONTIERS
Volume 5, Issue 18, Pages 7012-7021

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1qm00852h

Keywords

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Funding

  1. A*STAR under its Advanced Manufacturing and Engineering Program [A2083c0051]
  2. Ministry of Education, Singapore [MOE-MOET2EP10120-0007]
  3. SUTD-ZJU IDEA Grant [SUTD-ZJU (VP) 201905]
  4. National Natural Science Foundation of China [22078314, 21878286, 21908216]
  5. Dalian Institute of Chemical Physics [DICPI201938, DICPZZBS201805]
  6. Fujian Province Natural Science Foundation [2019J01757]

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Tetrazine-based fluorogenic probes are powerful tools in bioimaging, biosensing, and medical diagnostics. Understanding the fluorescence quenching mechanism is crucial for enhancing turn-on ratios of these probes. Utilizing the ETDS mechanism, we demonstrated key factors for improving the turn-on ratios of tetrazine-based fluorophores.
Tetrazine-based fluorogenic probes are powerful tools for bioimaging, biosensing, and medical diagnostic applications. In these probes, the attachment of a tetrazine moiety generates a non-fluorescent precursor; upon the bio-orthogonal reaction of the tetrazine fragment, a strong fluorescence signal is released from the fluorophore, resulting in significant fluorescence turn-on responses. To rationally design tetrazine-based probes with enhanced turn-on ratios, one fundamental challenge is to understand their fluorescence quenching mechanism. Herein, utilizing quantum chemistry calculations, we investigated and described a generalized fluorescence quenching mechanism, coined as energy transfer to a dark state (ETDS). With the aid of the ETDS mechanism, we demonstrated how a large excited-state energy gap and a short distance between a tetrazine group and a fluorophore are essential for increasing the rate of energy transfer and improving turn-on ratios of tetrazine-based fluorophores. We further proposed two strategies in the rational design of highly desirable fluorogenic probes that exhibit longer emission wavelengths and higher turn-on ratios, including (1) shortening the fluorophore-tetrazine distance via face-to-face stacking; and (2) modulating the UV-vis absorption wavelengths. Our calculation results could provide invaluable insights into the rational design of a new generation of tetrazine-based fluorogenic probes.

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