FLIM - Lifetime imaging - effect of multimerization of a fluorescence protein

Hello everybody,

Does anybody know a good resource describing the effect of multimerization (dimerization) on the lifetime of a fluorophore. Something like the theory or the measurement of the lifetime of GFP vs a dimer of GFP in solution ? (no FRET, just a single fluorophore / FP being multimerized.)

Thanks!

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This paper (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2770629/pdf/main.pdf) states:

“Because homo-FRET concerns energy transfer between identical fluorophores, it does not affect the emission spectrum or the fluorescence lifetime of the probes.”

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This is what I’ve heard from the experts in the field as well. Perhaps there’s some proof in older work. I wouldn’t be surprised if this is explained in “Principles of fluorescence spectroscopy” by Joseph R. Lakowicz (but I don’t have a copy at home, so I cannot check it).

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Perhaps these references are useful:
https://www.nature.com/articles/srep33022
https://dx.doi.org/10.1016%2FS0006-3495(01)76265-0

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