Fluorescent protein resource
Thermostable fluorescent protein
- Sea cactus thermostable green fluorescent protein, CoGFP
Thermostable fluorescent protein and its utility.
Murai M, Ogoh K, Kinebuchi T, Suzuki H.
Japan patent unregistered 2014-60947.
Upper, before heating. Lower, after heating at 100℃ for 10 minutes.
Observed at room temperature.Relative fluorescent intencity. 25℃ 70℃ 100℃ GFP of A. victoria 1072 1087 629 WT 4770 4229 703 Th1wt 8067 7236 2162 Th2wt 7668 7525 3711 Catalog no. Name of clone Characteristic RDB14364 pCoGFP-Th1wt wild type RDB14366 pCoGFP-Th2wt wild type RDB14365 pCoGFP-Th1co Optimize codons for transfection into mammalian cells RDB14367 pCoGFP-Th2co Optimize codons for transfection into mammalian cells
Non-fluorescent chromoprotein
| Protein | Resource (cat.num.) | Reference |
|---|---|---|
| cjBlue (Cnidopus japonicus) | cjBlue/pRSETB (RDB15242) cjBlue Y64L/pRSETB (RDB15243) |
Structural characterization of a blue chromoprotein and its yellow mutant from the sea anemone Cnidopus japonicus. Chan, M.C. et al., J. Biol. Chem. 281 (49): 37813-37819 (2006). PubMed PMID 17028187. |
Fluorescent protein
| Protein | Resource (cat.num.) | Reference |
|---|---|---|
| Midoriishi-Cyan (Acropara sp.) | MiCy/pRSETB (RDB15239) mMiCy1/pRSETB (RDB15241) |
Cyan-emitting and orange-emitting fluorescent proteins as a donor/acceptor pair for fluorescence resonance energy transfer. Karasawa, S. et al., Biochem. J. 381 (Pt 1): 307-312 (2004). PubMed PMID 15065984. |
| Azami Green (Galaxeidae sp.) | AG/pRSETB (RDB15228) hmAG407/pRSETB (RDB15229) hmAG1/pRSETB (RDB15230). |
A green-emitting fluorescent protein from Galaxeidae coral and its monomeric version for use in fluorescent labeling. Karasawa, S. et al., J. Biol. Chem. 278 (36): 34167-34171 (2003). PubMed PMID 12819206. |
| Cy11.5 (Aequorea victoria) | Cy11.5/pRSETB (RDB15706) | Concatenation of cyan and yellow fluorescent proteins for efficient resonance energy transfer. Shimozono, S. et al., Biochemistry 45 (20): 6267-6271 (2006). PubMed PMID 16700538. |
| Venus (Aequorea victoria) | Venus/pCS2 (RDB15116) mVenus/pRSETB (RDB15117) |
A variant of yellow fluorescent protein with fast and efficient maturation for cell-biological applications. Nagai, T. et al., Nat. Biotechnol. 20 (1): 87-90 (2002). PubMed PMID 11753368. |
| Venus (Aequorea victoria) | cp49Venus (RDB15120) cp145Venus (RDB15121) cp157Venus (RDB15122) cp173Venus (RDB15123) cp195Venus (RDB15124) cp229Venus (RDB15125) |
Expanded dynamic range of fluorescent indicators for Ca(2+) by circularly permuted yellow fluorescent proteins. Nagai, T. et al., Proc. Natl. Acad. Sci. U.S.A. 101 (29): 10554-10559 (2004). PubMed PMID 15247428. |
| Kusabira Green Orange (Fungia concinna) | mK-GO (RDB15244) | Age-dependent preferential dense-core vesicle exocytosis in neuroendocrine cells revealed by newly developed monomeric fluorescent timer protein. Tsuboi, T. et al., Mol. Biol. Cell. 21 (1): 87-94 (2010). PubMed PMID 19889833. |
| Kusabira Orange (Fungia concinna) | KO1/pRSETB (RDB15311) hmKO1/pRSETB (RDB15312) hmKO2/pRSETB (RDB15313) |
Cyan-emitting and orange-emitting fluorescent proteins as a donor/acceptor pair for fluorescence resonance energy transfer. Karasawa, S. et al., Biochem. J. 381 (Pt 1): 307-312 (2004). PubMed PMID 15065984. |
| Kusabira Orange (Fungia concinna) | hmKO-K/pRSETB (RDB15314) | Improving membrane voltage measurements using FRET with new fluorescent proteins. Tsutsui, H. et al., Nat. Methods 5 (8): 683-685 (2008). PubMed PMID 18622396. |
| Keima-red (Montipora. sp) | tdKeima/pRSETB (RDB15232) mKeima/pcDNA3 (RDB15233) dKeima/pRSETB (RDB15234) dKeima570/pRSETB (RDB15235) |
A fluorescent variant of a protein from the stony coral Montipora facilitates dual-color single-laser fluorescence cross-correlation spectroscopy. Kogure, T. et al., Nat. Biotechnol. 24 (5): 577-581 (2006). PubMed PMID 16648840. |
| Keima-red (Montipora. sp) | mKeima (h)/pCS2 (RDB15236) dKeima (h)/pCS2 (RDB15237) |
A sensitive and quantitative technique for detecting autophagic events based on lysosomal delivery. Katayama, H. et al., Chem. Biol. 18 (8): 1042-1052 (2011). PubMed PMID 21867919. |
| UnaG (Anguilla japonica) | UnaG/pcDNA3-FLAG (RDB15703) UnaG/pGEX-2T (RDB15704) |
A bilirubin-inducible fluorescent protein from eel muscle. Kumagai, A. et al., Cell 153 (7): 1602-1611(2013). PubMed PMID 23768684. |
| UnaG (Anguilla japonica) | pET-His UNAG (RDB13504) | Continuous de novo biosynthesis of haem and its rapid turnover to bilirubin are necessary for cytoprotection against cell damage. Takeda, T.A. et al., Sci. Rep. 5: 10488 (2015). PubMed PMID 25990790. |
Photoswitchable fluorescent protein
| Protein | Resource (cat.num.) | Reference |
|---|---|---|
| Dronpa-Green (Echinophyllia sp.) | Dronpa/pRSETB (RDB15256) 22G/pRSETB (RDB15255) |
Regulated fast nucleocytoplasmic shuttling observed by reversible protein highlighting. Ando, R. et al., Science 306 (5700): 1370-1373 (2004). PubMed PMID 15550670. |
| Dronpa-Green (Echinophyllia sp.) | Dronpa2/pRSETB (RDB15257) Dronpa3/pRSETB (RDB15258) |
Highlighted generation of fluorescence signals using simultaneous two-color irradiation on Dronpa mutants. Ando, R. et al., Biophys. J. 92 (12): L97-99 (2007). PubMed PMID 17384059. |
Photoconvertible fluorescent protein
| Protein | Resource (cat.num.) | Reference |
|---|---|---|
| Kaede (Trachyphyllia geoffroyi) | Kaede/pRSETB (RDB15231) | An optical marker based on the UV-induced green-to-red photoconversion of a fluorescent protein. Ando, R. et al., Proc. Natl. Acad. Sci. U.S.A. 99 (20): 12651-12656 (2002). PubMed PMID 12271129. |
| Kikume Green-Red (Favia favus) | KikGR/pRSETB (RDB15259) | Semi-rational engineering of a coral fluorescent protein into an efficient highlighter. Tsutsui, H. et al., EMBO Rep. 6 (3): 233-238 (2005). PubMed PMID 15731765. |
| Kikume Green-Red (Favia favus) | mKikGR/pRSETB (RDB15261) | mKikGR, a monomeric photoswitchable fluorescent protein. Habuchi, S. et al., PLoS One 3 (12): e3944 (2008). PubMed PMID 19079591. |
| h41pkve6 (derivative of Kikume Green-Red) (Favia favus) | Xpa (RDB15264) Xpa H62Q (RDB15265) |
A diffraction-quality protein crystal processed as an autophagic cargo. Tsutsui, H. et al., Mol. Cell 58 (1): 186-193 (2015). PubMed PMID 25773597. |
Tools
- Destabilized FPs
- Knock in markers with CRISPR/Cas9 genome editing
- As a part of Auxin Inducible Degron (AID) System clones, Dr. Masato Kanemaki provides a series of knock-in fluorescent and selection markers with CRISPR/Cas9 genome editing.
References
Sensor & Visualization
- Sensor & Visualization
- Bilirubin indicator UnaG, BReleaCa
- cAMP indicator
- Caspase activity indicator
- pH sensor
- Protein concentration in cells
- RA indicator
- Voltage indicator
- Autophagy indicator
- Chaperone mediated autophagy activity by the GAPDH-HT indicator by Dr. Takahiro Seki’s lab as well as fluorescent protein probes of LC3B accumulation developed by Dr. Noboru Mizushima’s lab, Dr. Itaru Hamachi’s lab and Dr. Keiji Kimura’s lab are available.
- Calcium-ion sensor
- Fluorescent protein-based Ca2+ sensors, G-CaMPs, Yellow Cameleons and Pericams developed by Dr. Jin-ichi Nakai’s lab and Dr. Atsushi Miyawaki’s lab, which are composed with calmodulin, fluorescent protein and M13 peptide (CaM binding domain of myosin light chain kinase), are designated to visualize intracellular [Ca2+] dynamics.
- G-CaMP
- Pericam
- Yellow Cameleon
- Cell cycle indicator Fucci
- To monitor cell cycle progression in living cells, cell cycle indicator Fucci probes deveoped by Dr. Atsushi Miyawaki’s lab are available.
- Epigenetics reporter
- Visualization of histone acetylation: The Histac fluorescent probes deposited by Dr. Kazuki Sasaki allow you monitoring the state of activity of acetylation of histone H4 by fluorescence in living cells.
- Visualization of methylated DNA: The EGFP-MBD-nls protein recognizes the methylated DNA and you can follow status of the DNA methylation in situ under physiological conditions using the pEGFP-MBD-nls expression clone.
- Knock in markers with CRISPR/Cas9 genome editing
- As a part of Auxin Inducible Degron (AID) System clones, Dr. Masato Kanemaki provides a series of knock-in fluorescent and selection markers with CRISPR/Cas9 genome editing.
- Notch signaling reporter
- The pRBS-EGFP and RBP-J-Venus expression clones deposited by Dr. Makoto Mark Taketo and Dr. Kenji Tanigaki, respectively, allow you monitoring the state of activation of the Notch signaling by fluorescence in living cells.
- Organelle marker/subcellular localization
- We are providing genetic resources for visualization of organelles such as mitochondria and nucleus. Each clone contains an organelle localization signal sequence fused with fluorescent proteins or epitope tags. Organelles can be detected by fluorescence or by detecting epitope tags with antibodies.
- Visualization of organelle contact sites using the organelle-targeted split-GFP system developed by Dr. Yasushi Tamura
- Sphingolipid marker
- Lipid rafts are small lipid domains on the cell membrane and are thought to play an important role in signal transduction, endocytosis and more. We provide fluorescent probes for sphingomyelin and cholesterol lipid domains.
- Nakanori: sphingomyelin and cholesterol lipid domain (lipid raft)
- D4 toxin: cholesterol rich domain
- lysenin: sphingomyelin
Luminescent protein
- Nano-lantern luminescent and fluorescent protein
- Nano lantern (NL) consists of Renilla luciferase and adjacent fluorescence protein. The chemiluminescence of the luciferase provides light source for excitation and enables the fluorescence protein to be observed. Three colors of NLs, yellow, cyan and orange, have been developed. NLs do not require external light source and overcome problems such as autofluorescence, phototoxicity, and photobleaching.
- Higher intensity luciferases having Green-, Yellow- or Red-emission by using D-luciferin
- These luciferases have at most four-time maximum luminous intensity than that of widely used luciferase of the Photinus pyralis, a common North American firefly. Further more, Green-, Yellow- or Red-emission can be obtained by using D-luciferin as a substrate of each luciferase.
- AkaLuc luciferase providing brighter and red-shifted luminescence
- The artificial bioluminescence system AkaBLI enables noninvasive signal observation in deep tissue of living animals. It was developed by Dr. Atsushi Miyawaki and Dr. Satoshi Iwano of the RIKEN Center for Brain Science, and Dr. Shojiro Maki of the University of Electro-Communications. The AkaBLI consists of an artificial substrate AkaLumine with improved tissue permeability and an artificial luciferase Akaluc optimized to AkaLumine. The intensity of the luminescence of AkaBLI system is 100 to 1000 folds brighter than the conventional systems.
(GRP0050e 2013.06.23 T.M.)
2019.02.09