Abstract
Fluorescence microscopy has been widely applied in the life sciences. While intensity as a steady-state signal is widely used, the time-resolved (tr) signal using fluorescence lifetime remains underexplored. Herein, we present a family of time-resolved fluorescent proteins (tr-FPs) with rationally controlled lifetimes. Using a strategy that regulates lifetime without affecting the spectra of FPs, we have developed a series of tr-FPs that cover the visible spectrum and a wide range of lifetimes. The tr-FPs are employed in temporal-spectral resolved microscopy, allowing for the simultaneous imaging of 9 different proteins in live cells and the correlation of multiple activities to cell cycles. Furthermore, tr-FPs enable multiplexing super-resolution microscopy that concurrently visualizes 4 proteins using the lifetime signal and are demonstrated to quantify the stoichiometry of cellular proteins. Our work introduces the concept and development of tr-FPs as a transformative toolset, presenting opportunities to integrate system complexity and quantitative accuracy into biological research.
| Original language | English |
|---|---|
| Pages (from-to) | 6987-7005.e28 |
| Journal | Cell |
| Volume | 188 |
| Issue number | 24 |
| DOIs | |
| State | Published - 26 Nov 2025 |
Keywords
- cell cycle
- ferroptosis
- fluorescence lifetime
- fluorescence lifetime microscopy
- multiplexed imaging
- oxidative stress
- protein stoichiometry quantification
- quantitative imaging
- super-resolution microscopy
- time-resolved fluorescent protein