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SNAP-tag2: faster and brighter protein labeling
Open accessPreprint — published as 10.1038/s41589-025-01942-z · Paper page
Abstract
SNAP-tag is a powerful tool for labeling proteins with synthetic fluorophores in bioimaging. However, its utility in live-cell applications can be constrained by its relatively slow labeling kinetics and the limited cell permeability of its substrates. Here we introduce new labeling substrates and an engineered SNAP-tag for faster labeling in vitro and in live cells. SNAP-tag2 presents a second-order rate constant with rhodamine substrates that approaches 10 7 s -1 M -1 , a 100-fold improvement over the corresponding SNAP-tag-substrate pairs. When labeled with highly fluorogenic dyes, SNAP-tag2 also shows a 5-fold increase in fluorescence brightness relative to currently used SNAP-tag. The increased labeling kinetics and brightness of SNAP-tag2 translates into a greatly improved performance in various live-cell (super-resolution) imaging applications.
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Metadata
- Authors
- Kühn, S., Nasufovic, V., Wilhelm, J., Kompa, J., de Lange, E. M. F., Lin, Y.-H., Egoldt, C., Fischer, J., Lennoi, A., Tarnawski, M., Reinstein, J., Vlijm, R., Hiblot, J., & Johnsson, K.
- Affiliations
- Max Planck Institute for Medical Research (DE)
- University of Groningen (NL)
- Corresponding author
- Hiblot, Julien
- Johnsson, Kai
- ORCID
- Venue
- Nature Chemical Biology
- Publisher
- openRxiv
- Published
- 2024-08-29
- Volume
- 21
- Issue
- 11
- Pages
- 1754-1761
- ISSN
- 1552-4450 (ISSN-L)
- PMC
- PMC12568630
- OpenAlex
- W4412008163
- Cited by
- 44
- References
- 1
- Citations by year
- 2026: 26 · 2025: 18
- FWCI
- 16.59
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Nature Chemical Biology (publishedVersion, cc-by)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed (publishedVersion)
- University of Groningen research database (University of Groningen / Centre for Information Technology) (submittedVersion, cc-by)
- Funders
- Deutsche Forschungsgemeinschaft (TRR186)
- École Polytechnique Fédérale de Lausanne
- Max-Planck-Gesellschaft
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biophysics › Advanced Fluorescence Microscopy Techniques
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Biochemical and Structural Characterization
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Biotin and Related Studies
- Keywords
- SNAP-tag, protein labeling, fluorogenic dyes, fluorescence intensity, live-cell imaging, super-resolution imaging, membrane permeability
- MeSH terms
- Animals, Fluorescent Dyes, Humans, Kinetics, Proteins, Rhodamines, Staining and Labeling
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