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Photoactivatable fluorescent protein


Photoactivatable fluorescent proteins (PAFPs) is a type of fluorescent protein that exhibit fluorescence that can be modified by a light-induced chemical reaction.

History

The first PAFP, Kaede (protein), was isolated from Trachyphyllia geoffroyi in a cDNA library screen designed to identify new fluorescent proteins. A fluorescent green protein derived from this screen was serendipitously discovered to have sensitivity to ultraviolet light--

We happened to leave one of the protein aliquots on the laboratory bench overnight. The next day, we found that the protein sample on the bench had turned red, whereas the others that were kept in a paper box remained green. Although the sky had been partly cloudy, the red sample had been exposed to sunlight through the south-facing windows.

Properties

Many PAFPs have been engineered from existing fluorescent proteins or identified from large-scale screens in the wake of Kaede's discovery. Many of these undergo green-to-red photoconversion, but other colors are available. Some proteins take part in irreversible photoconversion reactions while other reactions can be reversed using light of a specific wavelength.

List of PAFPs

PAFP PropertiesPAFPAbsorbance1 (nm)Emission1 (nm)Absorbance2 (nm)Emission2 (nm)Photoconversion wavelengthReversibilityBrightness1*Brightness2*Reference518580516581516580516?580?517593518??517468511?600*Brightness values are relative to EGFP.
Kaede (protein)508572ultravioletnone2.64X0.60X
Eos (protein)506571ultravioletnone1.30X0.70X
IrisFP488551ultravioletnone0.66X0.49X
IrisFP488390490 nmreversible, 390 nm??idem
IrisFP551440550 nmreversible, 440 nm??idem
KikGR/Kikume507583ultravioletnone0.60X0.64X
Dronpa503390490 nmreversible, 390 nm??
PAGFP400504ultravioletnone0.08X0.42X
PS-CFP402490ultravioletnone0.17X0.16X
KFP1?590greenvariable0.004X0.13X

Applications

Unlike other fluorescent proteins, PAFPs can be used as selective optical markers. An entirely labeled cell can be followed to assess cell division, migration, and morphology. Very small volumes containing PAFPs can be activated with a laser. In these cases, protein trafficking, diffusion, and turnover can be assessed.

References

References

  1. (2002-10-01). "An optical marker based on the UV-induced green-to-red photoconversion of a fluorescent protein". Proceedings of the National Academy of Sciences.
  2. (November 2005). "Photoactivatable fluorescent proteins". Nature Reviews Molecular Cell Biology.
  3. (2004-11-09). "EosFP, a fluorescent marker protein with UV-inducible green-to-red fluorescence conversion". Proceedings of the National Academy of Sciences.
  4. (2008-11-25). "Structural characterization of IrisFP, an optical highlighter undergoing multiple photo-induced transformations". Proceedings of the National Academy of Sciences.
  5. (March 2005). "Semi-rational engineering of a coral fluorescent protein into an efficient highlighter". EMBO Reports.
  6. (2005-07-05). "Reversible single-molecule photoswitching in the GFP-like fluorescent protein Dronpa". Proceedings of the National Academy of Sciences.
  7. (April 2004). "Selective photolabeling of proteins using photoactivatable GFP". Methods.
  8. (2004-11-01). "Photoswitchable cyan fluorescent protein for protein tracking". Nature Biotechnology.
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