On/off blinking and switching behaviour of single molecules of green fluorescent protein

Robert M. Dickson, Andrew B. Cubitt, Roger Y. Tsien and W. E. Moerner ()
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Robert M. Dickson: University of California San Diego
Andrew B. Cubitt: †Aurora Biosciences
Roger Y. Tsien: University of California San Diego
W. E. Moerner: University of California San Diego

Nature, 1997, vol. 388, issue 6640, 355-358

Abstract: Abstract Optical studies of individual molecules at low and room temperature can provide information about the dynamics of local environments in solids, liquids and biological systems unobscured by ensemble averaging1,2,3,4,5,6,7,8,9,10,11,12,13,14. Here we present a study of the photophysical behaviour of single molecules of the green fluorescent protein (GFP) derived from the jellyfish Aequorea victoria. Wild-type GFP and its mutant have attracted interest as fluorescent biological labels because the fluorophore may be formed in vivo15,16. GFP mutants immobilized in aereated aqueous polymer gels and excited by 488-nm light undergo repeated cycles of fluorescent emission (‘blinking’) on a timescale of several seconds—behaviour that would be unobservable in bulk studies. Eventually the individual GFP molecules reach a long-lasting dark state, from which they can be switched back to the original emissive state by irradiation at 405 nm. This suggests the possibility of using these GFPs as fluorescent markers for time-dependent cell processes, and as molecular photonic switches or optical storage elements, addressable on the single-molecule level.

Date: 1997
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DOI: 10.1038/41048

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