Far-red fluorescent tags for protein imaging in living tissues

Author:

Shcherbo Dmitry1,Murphy Christopher S.2,Ermakova Galina V.1,Solovieva Elena A.1,Chepurnykh Tatiana V.3,Shcheglov Aleksandr S.1,Verkhusha Vladislav V.4,Pletnev Vladimir Z.1,Hazelwood Kristin L.2,Roche Patrick M.2,Lukyanov Sergey1,Zaraisky Andrey G.1,Davidson Michael W.2,Chudakov Dmitriy M.1

Affiliation:

1. Shemiakin-Ovchinnikov Institute of Bioorganic Chemistry, Miklukho-Maklaya 16/10, 117997 Moscow, Russia

2. National High Magnetic Field Laboratory and Department of Biological Science, Florida State University, 1800 E. Paul Dirac Dr., Tallahassee, FL 32310, U.S.A.

3. Evrogen JSC, Miklukho-Maklaya 16/10, Moscow 117997, Russia

4. Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY 10461, U.S.A.

Abstract

A vast colour palette of monomeric fluorescent proteins has been developed to investigate protein localization, motility and interactions. However, low brightness has remained a problem in far-red variants, which hampers multicolour labelling and whole-body imaging techniques. In the present paper, we report mKate2, a monomeric far-red fluorescent protein that is almost 3-fold brighter than the previously reported mKate and is 10-fold brighter than mPlum. The high-brightness, far-red emission spectrum, excellent pH resistance and photostability, coupled with low toxicity demonstrated in transgenic Xenopus laevis embryos, make mKate2 a superior fluorescent tag for imaging in living tissues. We also report tdKatushka2, a tandem far-red tag that performs well in fusions, provides 4-fold brighter near-IR fluorescence compared with mRaspberry or mCherry, and is 20-fold brighter than mPlum. Together, monomeric mKate2 and pseudo-monomeric tdKatushka2 represent the next generation of extra-bright far-red fluorescent probes offering novel possibilities for fluorescent imaging of proteins in living cells and animals.

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry

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