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Abstract
Two distinct fusion proteins were recruited to a target RNA inside living cells using engineered self-labeling enzymes.
- Combining two orthogonal self-labeling enzymes allowed for concurrent assembly and disassembly of guide RNA-protein conjugates.
- The approach enables control of RNA-targeting through light activation.
- A photo-induced swap of two distinct RNA editing events was achieved.
- This work highlights potential innovations in tool development, RNA imaging, and transcript engineering.
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