CellBiochemistryPeer-reviewed journal article
Time-resolved fluorescent proteins towards fluorescence microscopy in the temporal and spectral domains
Zizhu Tan, Chia‐Heng HsiungiD, Jiahui Feng, Yangye Zhang, Yihan WaniD, Junlin CheniD, Ke SuniD, Peilong LuiD, Jianyang Zang, Wen‐Xing YangiD, Ya GaoiD, Jiabin Yin, Tong Zhu, Lu YangiD, Zijian PaniD, Yilong ZouiD, Can Liao, Xiaosong LiiD, Yuxuan YeiD, Yu LiuiD, Xin ZhangiD
Abstract
Fluorescence microscopy has been widely applied in life sciences. While steady-state fluorescence intensity is mostly used, the time-resolved detection mode relying on fluorescence lifetime remains underexplored. Herein, we present a family of time-resolved fluorescent proteins (TRFP). Using a strategy that regulates lifetime without affecting spectra of FPs, we have developed different TRFPs that cover the visible spectrum and a wide range of lifetime. TRFPs are employed in the temporal-spectral resolved microscopy, allowing the simultaneous imaging of 9 different proteins in live cells and correlation of multiple activities to cell cycles. Finally, TRFPs are integrated into multiplexing super-resolution microscopy to concurrently visualize 4 proteins in live cells, acquiring a remarkable 50 nm spatial resolution using lifetime as signal. TRFPs represent a transformative toolset towards fluorescence microscopy in both the temporal and spectral domains. Beyond the multiplexing imaging, TRFPs could introduce unprecedented opportunities of system complexity and quantitative accuracy into biological research.
- assay: fluorescence / live-cell microscopy
- research focus: cell type annotation
- research focus: clustering
- research focus: spatial domain detection
- approach: microscopy & imaging analysis
- Citations
- 23
- FWCI
- 7.96
- Field percentile
- top 1%
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