Multiplexed 3D FRET imaging in deep tissue of live embryos
- Zhao, M., Wan, X., Li, Y., Zhou, W., Peng, L.
- Scientific Reports 5: 13991 (Journal)
- Registered Authors
- Li, Yu, Wan, Xiaoyang, Zhou, Weibin
- Fluorescence imaging, Transgenic organisms
- MeSH Terms
- Animals, Genetically Modified
- Embryo, Nonmammalian/metabolism*
- Fluorescence Resonance Energy Transfer/methods*
- Fluorescent Dyes
- Imaging, Three-Dimensional/methods*
- Microscopy, Fluorescence/methods
- 26387920 Full text @ Sci. Rep.
Zhao, M., Wan, X., Li, Y., Zhou, W., Peng, L. (2015) Multiplexed 3D FRET imaging in deep tissue of live embryos. Scientific Reports. 5:13991.
Current deep tissue microscopy techniques are mostly restricted to intensity mapping of fluorophores, which significantly limit their applications in investigating biochemical processes in vivo. We present a deep tissue multiplexed functional imaging method that probes multiple Förster resonant energy transfer (FRET) sensors in live embryos with high spatial resolution. The method simultaneously images fluorescence lifetimes in 3D with multiple excitation lasers. Through quantitative analysis of triple-channel intensity and lifetime images, we demonstrated that Ca(2+) and cAMP levels of live embryos expressing dual FRET sensors can be monitored simultaneously at microscopic resolution. The method is compatible with a broad range of FRET sensors currently available for probing various cellular biochemical functions. It opens the door to imaging complex cellular circuitries in whole live organisms.
Genes / Markers
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Engineered Foreign Genes