The DOI matches its Crossref record; 18 of the 18 references it cites were found in a registry or an index.
Rapid blue-light–mediated induction of protein interactions in living cells
Open accessAbstract
Dimerizers allowing inducible control of protein-protein interactions are powerful tools for manipulating biological processes. Here we describe genetically encoded light-inducible protein-interaction modules based on Arabidopsis thaliana cryptochrome 2 and CIB1 that require no exogenous ligands and dimerize on blue-light exposure with subsecond time resolution and subcellular spatial resolution. We demonstrate the utility of this system by inducing protein translocation, transcription and Cre recombinase–mediated DNA recombination using light.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Spatiotemporal control of cell signalling using a light-switchable protein interaction
Levskaya, A., Weiner, O. D., Lim, W. A., & Voigt, C. A. (2009) · Nature · doi:10.1038/nature08446 · Cited by 1,009
Controlling Signal Transduction with Synthetic Ligands
Spencer, D. M., Wandless, T. J., Schreiber, S. L., & Crabtree, G. R. (1993) · Science · doi:10.1126/science.7694365 · Cited by 843
Photoexcited CRY2 Interacts with CIB1 to Regulate Transcription and Floral Initiation in Arabidopsis
Liu, H., Yu, X., Li, K., Klejnot, J., Yang, H., Lisiero, D., & Lin, C. (2008) · Science · doi:10.1126/science.1163927 · Cited by 719
A light-switchable gene promoter system
Shimizu-Sato, S., Huq, E., Tepperman, J. M., & Quail, P. H. (2002) · Nature Biotechnology · doi:10.1038/nbt734 · Cited by 617
Biochemical and genetic analysis of the yeast proteome with a movable ORF collection
Gelperin, D. M., White, M. A., Wilkinson, M. L., Kon, Y., Kung, L. A., Wise, K. J., Lopez-Hoyo, N., Jiang, L., Piccirillo, S., Yu, H., et al. (2005) · Genes & Development · doi:10.1101/gad.1362105 · Cited by 483
Cryptochrome Blue Light Photoreceptors Are Activated through Interconversion of Flavin Redox States
Bouly, J.-P., Schleicher, E., Dionisio-Sese, M., Vandenbussche, F., Van Der Straeten, D., Bakrim, N., Meier, S., Batschauer, A., Galland, P., Bittl, R., et al. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m609842200 · Cited by 441
Induction of protein-protein interactions in live cells using light
Yazawa, M., Sadaghiani, A. M., Hsueh, B., & Dolmetsch, R. E. (2009) · Nature Biotechnology · doi:10.1038/nbt.1569 · Cited by 376
Khanna, R., Huq, E., Kikis, E. A., Al-Sady, B., Lanzatella, C., & Quail, P. H. (2004) · The Plant Cell · doi:10.1105/tpc.104.025643 · Cited by 362
Syntaxin-4 defines a domain for activity-dependent exocytosis in dendritic spines
Kennedy, M. J., Davison, I. G., Robinson, C. G., & Ehlers, M. D. (2010) · Cell · doi:10.1016/j.cell.2010.02.042 · Cited by 294
Self-citationThe Signaling State of Arabidopsis Cryptochrome 2 Contains Flavin Semiquinone
Banerjee, R., Schleicher, E., Meier, S., Viana, R. M., Pokorny, R., Ahmad, M., Bittl, R., & Batschauer, A. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m700616200 · Cited by 262
Action Spectrum for Cryptochrome-Dependent Hypocotyl Growth Inhibition in Arabidopsis
Ahmad, M., Grancher, N., Heil, M., Black, R. C., Giovani, B., Galland, P., & Lardemer, D. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.010969 · Cited by 219
Sang, Y., Li, Q.-H., Rubio, V., Zhang, Y.-C., Mao, J., Deng, X.-W., & Yang, H.-Q. (2005) · The Plant Cell · doi:10.1105/tpc.104.029645 · Cited by 201
Regulation of Cre recombinase by ligand-induced complementation of inactive fragments
Jullien, N. (2003) · Nucleic Acids Research · doi:10.1093/nar/gng131 · Cited by 180
Unnatural Ligands for Engineered Proteins: New Tools for Chemical Genetics
Bishop, A., Buzko, O., Heyeck-Dumas, S., Jung, I., Kraybill, B., Liu, Y., Shah, K., Ulrich, S., Witucki, L., Yang, F., et al. (2000) · Annual Review of Biophysics and Biomolecular Structure · doi:10.1146/annurev.biophys.29.1.577 · Cited by 158
Activation of protein splicing with light in yeast
Tyszkiewicz, A. B., & Muir, T. W. (2008) · Nature Methods · doi:10.1038/nmeth.1189 · Cited by 154
Preparation of organotypic hippocampal slice cultures for long-term live imaging
Gogolla, N., Galimberti, I., Paola, V. D., & Caroni, P. (2006) · Nature Protocols · doi:10.1038/nprot.2006.168 · Cited by 136
Genetically encoded photoswitching of actin assembly through the Cdc42-WASP-Arp2/3 complex pathway
Leung, D. W., Otomo, C., Chory, J., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0801232105 · Cited by 104
Chemically Induced and Light-Independent Cryptochrome Photoreceptor Activation
Rosenfeldt, G., Muñoz‐Viana, R., Mootz, H. D., von Arnim, A. G., & Batschauer, A. (2007) · Molecular Plant · doi:10.1093/mp/ssm002 · Cited by 57
Cited by
Spatiotemporal Control of Intracellular Phase Transitions Using Light-Activated optoDroplets
Shin, Y., Berry, J., Pannucci, N., Haataja, M. P., Toettcher, J. E., & Brangwynne, C. P. (2017) · Cell · doi:10.1016/j.cell.2016.11.054 · Cited by 965
Optical control of mammalian endogenous transcription and epigenetic states
Konermann, S., Brigham, M. D., Trevino, A. E., Hsu, P. D., Heidenreich, M., Cong, L., Platt, R. J., Scott, D. A., Church, G. M., & Zhang, F. (2013) · Nature · doi:10.1038/nature12466 · Cited by 803
Yim, N., Ryu, S.-W., Choi, K., Lee, K. R., Lee, S., Choi, H., Kim, J., Shaker, M. R., Sun, W., Park, J.-H., et al. (2016) · Nature Communications · doi:10.1038/ncomms12277 · Cited by 578
Editing the epigenome: technologies for programmable transcription and epigenetic modulation
Thakore, P. I., Black, J. B., Hilton, I. B., & Gersbach, C. A. (2016) · Nature Methods · doi:10.1038/nmeth.3733 · Cited by 451
Role of Astrocytes in Neurovascular Coupling
Petzold, G. C., & Murthy, V. N. (2011) · Neuron · doi:10.1016/j.neuron.2011.08.009 · Cited by 409
Metadata
- Authors
- Kennedy, M. J., Hughes, R. M., Peteya, L. A., Schwartz, J. W., Ehlers, M. D., & Tucker, C. L.
- Venue
- Nature Methods
- Published
- 2010-10-31
- Volume
- 7
- Issue
- 12
- Pages
- 973-975
- ISSN
- 1548-7091 (ISSN-L)
- 1548-7105
- OpenAlex
- W2001831734
- Cited by
- 1,120
- References
- 18
- FWCI
- 37.84
- Type
- journal article
- Language
- en
- Open access
- green
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.