photobleaching
Sign in to saveright|thumb|Photobleaching: The movie shows photobleaching of a fluorosphere. The movie is accelerated, the whole process happened during 4 minutes. In optics, photobleaching (sometimes termed fading) is the photochemical alteration of a dye or a fluorophore molecule such that it is permanently unable to fluoresce. This is caused by cleaving of covalent bonds or non-specific reactions between the fluorophore and surrounding molecules. Such irreversible modifications in covalent bonds are caused by transition from a singlet state to the triplet state of the fluorophores. The number of excitatio
Research
11,422 papers- Lumos maxima - How robust fluorophores resist photobleaching?Current opinion in chemical biology · 2024
- Electrochemiluminescence Loss in Photobleaching.Angewandte Chemie (International ed. in English) · 2021
- Long-Term Fluorescence Recovery After Photobleaching (FRAP).Methods in molecular biology (Clifton, N.J.) · 2023
- Photobleaching and photoactivation: following protein dynamics in living cells.Nature cell biology · 2003
- Photobleaching microscopy reveals the dynamics of mRNA-binding proteins inside live cell nuclei.Progress in molecular and subcellular biology · 2004
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Encyclopedic overview
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right|thumb|Photobleaching: The movie shows photobleaching of a fluorosphere. The movie is accelerated, the whole process happened during 4 minutes. In optics, photobleaching (sometimes termed fading) is the photochemical alteration of a dye or a fluorophore molecule such that it is permanently unable to fluoresce. This is caused by cleaving of covalent bonds or non-specific reactions between the fluorophore and surrounding molecules. Such irreversible modifications in covalent bonds are caused by transition from a singlet state to the triplet state of the fluorophores. The number of excitation cycles to achieve full bleaching varies. In microscopy, photobleaching may complicate the observation of fluorescent molecules, since they will eventually be destroyed by the light exposure necessary to stimulate them into fluorescing. This is especially problematic in time-lapse microscopy.
However, photobleaching may also be used prior to applying the (primarily antibody-linked) fluorescent molecules, in an attempt to quench autofluorescence. This can help improve the signal-to-noise ratio.
Excerpted from Wikipedia’s “photobleaching” article, available under the CC BY-SA 4.0 licence.