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A Set of Novel Far-Red Fluorescent Proteins for Temporal Domain Multiplexing and Super-Resolution Imaging

Olumayowa FakoredeiD, Zhien Rong, Ruizhao WangiD, Stavrini PapadakiiD, Xinyue WangiD, Jiayue Cao, Fedor V. SubachiD, Reinhard Wolfgang KösteriD, Kazuhiko NamikawaiD, Kiryl D. PiatkevichiD

Abstract

The diverse spectral and photochemical properties of fluorescent proteins enable a variety of imaging applications in cell biology, ranging from cellular and organelle labeling to super-resolution microscopy and multiplexed live cell imaging. Here, we report a set of novel far-red fluorescent proteins, named mfRFP, mfRFP-A, and mCardinal-A, which are characterized by similar fluorescence spectra with excitation/emission at [~]600/660 nm while exhibiting distinct photobleaching rates. Differences in photostability allowed us to perform per-pixel unmixing of the three far-red FPs imaged simultaneously by employing a recently introduced temporal domain multiplexing approach. We demonstrated the application of the temporal domain multiplexing approach with different combinations of far-red fluorescent proteins possessing nearly identical emission spectra by acquiring BrainBow-like images of cellular populations and distinguishing subcellular structures in mammalian cells using a single imaging channel without applying any hardware modifications to the conventional microscope. Unlike previous temporal domain multiplying approaches employing photophysical properties of fluorescent proteins, the current approach is a wide range of microscopy modalities, including 3D imaging with a spinning disk and point scanning confocal microscopy. The most photostable fluorescent protein in the set, mfRFP, was further benchmarked against spectrally similar FPs and applied for super-resolution imaging of structural proteins in mammalian cells and for neuroimaging of model organisms, including mice, zebrafish, and C. elegans.

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