Evolution and characterization of a new reversibly photoswitching chromogenic protein, Dathail

Patricia S. Langan, Devin W. Close, Leighton Coates, Reginaldo C. Rocha, Koushik Ghosh, Csaba Kiss, Geoff Waldo, James Freyer, Andrey Kovalevsky, Andrew R.M. Bradbury

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

Abstract

We report the engineering of a new reversibly switching chromogenic protein, Dathail. Dathail was evolved from the extremely thermostable fluorescent proteins thermal green protein (TGP) and eCGP123 using directed evolution and ratiometric sorting. Dathail has two spectrally distinct chromogenic states with low quantum yields, corresponding to absorbance in a ground state with a maximum at 389 nm, and a photo-induced metastable state with a maximum at 497 nm. In contrast to all previously described photoswitchable proteins, both spectral states of Dathail are non-fluorescent. The photo-induced chromogenic state of Dathail has a lifetime of ~ 50 min at 293 K and pH 7.5 as measured by UV-Vis spectrophotometry, returning to the ground state through thermal relaxation. X-ray crystallography provided structural insights supporting a change in conformation and coordination in the chromophore pocket as being responsible for Dathail's photoswitching. Neutron crystallography, carried out for the first time on a protein from the green fluorescent protein family, showed a distribution of hydrogen atoms revealing protonation of the chromophore 4-hydroxybenzyl group in the ground state. The neutron structure also supports the hypothesis that the photo-induced proton transfer from the chromophore occurs through water-mediated proton relay into the bulk solvent. Beyond its spectroscopic curiosity, Dathail has several characteristics that are improvements for applications, including low background fluorescence, large spectral separation, rapid switching time, and the ability to switch many times. Therefore, Dathail is likely to be extremely useful in the quickly developing fields of imaging and biosensors, including photochromic Förster resonance energy transfer, high-resolution microscopy, and live tracking within the cell.

Original languageEnglish
Pages (from-to)1776-1789
Number of pages14
JournalJournal of Molecular Biology
Volume428
Issue number9
DOIs
StatePublished - May 8 2016

Funding

This research at ORNL's Spallation Neutron Source was sponsored by the Scientific User Facilities Division, Office of Basic Energy Sciences, U.S. Department of Energy . The Office of Biological and Environmental Research supported research at Oak Ridge National Laboratory's Center for Structural Molecular Biology, using facilities supported by the Scientific User Facilities Division, Office of Basic Energy Sciences, U.S. Department of Energy .

FundersFunder number
Scientific User Facilities Division
U.S. Department of Energy
Basic Energy Sciences
Oak Ridge National Laboratory

    Keywords

    • chromoprotein
    • ensemble refinement
    • neutron crystallography
    • pcFRET
    • photoswitchable

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