Bright ligand-activatable fluorescent protein for high-quality multicolor live-cell super-resolution microscopy.
Jiwoong KwonJong-Seok ParkMinsu KangSoobin ChoiJumi ParkGyeong Tae KimChangwook LeeSangwon ChaHyun-Woo RheeSang-Hee ShimPublished in: Nature communications (2020)
We introduce UnaG as a green-to-dark photoswitching fluorescent protein capable of high-quality super-resolution imaging with photon numbers equivalent to the brightest photoswitchable red protein. UnaG only fluoresces upon binding of a fluorogenic metabolite, bilirubin, enabling UV-free reversible photoswitching with easily controllable kinetics and low background under Epi illumination. The on- and off-switching rates are controlled by the concentration of the ligand and the excitation light intensity, respectively, where the dissolved oxygen also promotes the off-switching. The photo-oxidation reaction mechanism of bilirubin in UnaG suggests that the lack of ligand-protein covalent bond allows the oxidized ligand to detach from the protein, emptying the binding cavity for rebinding to a fresh ligand molecule. We demonstrate super-resolution single-molecule localization imaging of various subcellular structures genetically encoded with UnaG, which enables facile labeling and simultaneous multicolor imaging of live cells. UnaG has the promise of becoming a default protein for high-performance super-resolution imaging.
Keyphrases
- high resolution
- single molecule
- binding protein
- living cells
- amino acid
- induced apoptosis
- oxidative stress
- transcription factor
- machine learning
- nitric oxide
- cell death
- fluorescence imaging
- flow cytometry
- small molecule
- highly efficient
- photodynamic therapy
- big data
- single cell
- endoplasmic reticulum stress
- gold nanoparticles
- deep learning
- electron transfer
- organic matter
- resting state