Lee SY, Chea JS, Zhao BX, Xu C, Udeshi ND, Roh H, Kim C, Cho K, Carr SA, Ting A. 2022
The incorporation of light-responsive domains into engineered proteins has produced optogenetic tools with the ability to regulate protein localization, interactions, and function with light. We introduced this mode of regulation into proximity labeling (PL), which has been a cornerstone technique for high-resolution proteomic mapping of organelles and interactomes in living cells. Through a combination of structure-guided screening and yeast display directed evolution, we inserted the light sensitive LOV domain into a surface exposed loop of the PL enzyme TurboID to rapidly and reversibly control its labeling activity with low-power blue light. We showed that "LOV-Turbo" works in multiple organelles and cell types and can dramatically reduce background labeling in biotin-rich environments such as living neurons. We utilized LOV-Turbo's reversibility to perform pulse-chase labeling followed by organelle fractionation to discover endogenous proteins that traffick between endoplasmic reticulum, nuclear, and mitochondrial compartments under cellular stress. Lastly, we showed that instead of external light, LOV-Turbo can be activated by bioluminescence resonance energy transfer from proximal luciferase in living cells, opening the door to chemical and/or interaction dependent PL. Overall, LOV-Turbo increases the spatial and temporal precision of PL and expands the scope of experimental questions that can be addressed using PL.
[doi:10.25345/C5RR1PR89]
[dataset license: CC0 1.0 Universal (CC0 1.0)]
Keywords: TMT ; proximity labeling
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Principal Investigators: (in alphabetical order) |
Steven A. Carr, Broad Institute of MIT and Harvard, United States |
| Submitting User: | clauser |
Lee SY, Cheah JS, Zhao B, Xu C, Roh H, Kim CK, Cho KF, Udeshi ND, Carr SA, Ting AY.
Engineered allostery in light-regulated LOV-Turbo enables precise spatiotemporal control of proximity labeling in living cells.
bioRxiv. Epub 2023 Mar 9.
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