Abstract

Monomeric near-infrared (NIR) fluorescent proteins (FPs) are in high demand as protein tags and components of biosensors for deep-tissue imaging and multicolour microscopy. We report three bright and spectrally distinct monomeric NIR FPs, termed miRFPs, engineered from bacterial phytochrome, which can be used as easily as GFP-like FPs. miRFPs are 2–5-fold brighter in mammalian cells than other monomeric NIR FPs and perform well in protein fusions, allowing multicolour structured illumination microscopy. miRFPs enable development of several types of NIR biosensors, such as for protein–protein interactions, RNA detection, signalling cascades and cell fate. We demonstrate this by engineering the monomeric fluorescence complementation reporters, the IκBα reporter for NF-κB pathway and the cell cycle biosensor for detection of proliferation status of cells in culture and in animals. miRFPs allow non-invasive visualization and detection of biological processes at different scales, from super-resolution microscopy to in vivo imaging, using the same probes.

Highlights

  • Monomeric near-infrared (NIR) fluorescent proteins (FPs) are in high demand as protein tags and components of biosensors for deep-tissue imaging and multicolour microscopy

  • In engineered NIR FPs, the photoisomerization is blocked and the other non-radiative energy dissipation pathways are suppressed by truncation of bacterial phytochrome photoreceptors (BphP) to the chromophore-binding PAS-GAF domains and by introducing of amino-acid substitutions in the chromophore immediate environment[1,9]

  • To engineer miRFPs, we chose the chromophore-binding PAS-GAF domains of RpBphP1 as a starting point for molecular evolution

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Summary

Introduction

Monomeric near-infrared (NIR) fluorescent proteins (FPs) are in high demand as protein tags and components of biosensors for deep-tissue imaging and multicolour microscopy. BphP-based NIR FPs are widely used in many areas of basic and translational research, including cancer studies, stem cell biology, neuroscience and parasitology, these FPs are mainly serve as passive whole-cell labels for non-invasive in vivo imaging[5]. These NIR FPs had the limited use in monitoring of active cellular processes in animals, such as activation of signalling cascades and protein–protein interactions (PPIs). Available monomeric far-red GFP-like FPs, including mKate[2] (ref. 10), TagRFP657 (ref. 11), mCardinal and mNeptune2.5 (ref. 12), are suboptimal for deep-tissue imaging because their excitation maxima do not exceed 611 nm

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