Live-cell multiphoton fluorescence correlation spectroscopy with an improved large Stokes shift fluorescent protein

Abstract

We report an improved variant of mKeima, a monomeric long Stokes shift red fluorescent protein, hmKeima8.5. The increased intracellular brightness and large Stokes shift (∼180 nm) make it an excellent partner with teal fluorescent protein (mTFP1) for multiphoton, multicolor applications. Excitation of this pair by a single multiphoton excitation wavelength (MPE, 850 nm) yields well-separable emission peaks (∼120-nm separation). Using this pair, we measure homo- and hetero-oligomerization interactions in living cells via multiphoton excitation fluorescence correlation spectroscopy (MPE-FCS). Using tandem dimer proteins and small-molecule inducible dimerization domains, we demonstrate robust and quantitative detection of intracellular protein-protein interactions. We also use MPE-FCCS to detect drug-protein interactions in the intracellular environment using a Coumarin 343 (C343)-conjugated drug and hmKeima8.5 as a fluorescence pair. The mTFP1/hmKeima8.5 and C343/hmKeima8.5 combinations, together with our calibration constructs, provide a practical and broadly applicable toolbox for the investigation of molecular interactions in the cytoplasm of living cells.

DOI: 10.1091/mbc.E14-10-1473

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Cite this paper

@inproceedings{Guan2015LivecellMF, title={Live-cell multiphoton fluorescence correlation spectroscopy with an improved large Stokes shift fluorescent protein}, author={Yinghua Guan and Matthias Meurer and Sarada Raghavan and Aleksander K Rebane and Jake R. Lindquist and Sofia A. Santos and Ilia Kats and Michael W. Davidson and Ralph Mazitschek and Thomas E Hughes and Mikhail A Drobizhev and Michael Knop and Jagesh V. Shah and Diane S. Lidke}, booktitle={Molecular biology of the cell}, year={2015} }