Development of programmable RNA imaging with RNA-guided GFP via click chemistry
The CRISPR-Cas system revolutionized molecular biology by guiding Cas proteins to target nucleic acid sequences using customizable guide RNAs, offering unparalleled precision and versatility. Inspired by this innovation, we developed RNA-guided green fluorescent protein (RGG), a simple and programmable platform for targeting nucleic acid. Using a streamlined click chemistry approach, known for its high efficiency and specificity, we conjugated dibenzocyclooctyne (DBCO)-modified guide nucleic acids, designed to complement target sequences, with azide-exposed proteins to construct RGG. Systematic optimization identified 30-nt RNA with 3'-DBCO modifications as the most effective configuration for RGG, enabling precise visualization of nuclear-localized RNAs, including NEAT1 and Satellite III RNA, in living cells. This establishes RGG as a customizable and efficient system for RNA imaging and molecular analysis, underscoring the potential of direct conjugation between guide nucleic acids and proteins to enable precise nucleic acid recognition and dynamic molecular modification in living cells.
Authors
- Jun Nakamura (ORCID: https://orcid.org/0000-0002-9319-9973)
- Junpei Yamamoto (ORCID: https://orcid.org/0000-0002-5036-991X)
- Miyako Shiraishi (ORCID: https://orcid.org/0000-0002-5782-1649)
- Keiichiro Suzuki (ORCID: https://orcid.org/0000-0001-5603-9105)
Institutions
- Kyushu University (JP)
- Toneyama National Hospital (JP)
- The University of Osaka (JP)
Publication Details
- Journal
- Nucleic Acids Research
- Published
- 2025-10-28
- DOI
- https://doi.org/10.1093/nar/gkaf1147
- Primary Topic
- Click Chemistry and Applications
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Uehara Memorial Foundation
- Japan Society for the Promotion of Science