Abstract
Martensitic transformations are the first-order crystal-to-crystal phase transitions that occur mostly in materials such as steel, alloys and ceramics, thus having many technological applications. These phase transitions are rarely observed in molecular crystals and have not been detected in protein crystals. Reversibly switchable fluorescent proteins are widely used in biotechnology, including super-resolution molecular imaging, and hold promise as candidate biomaterials for future high-tech applications. Here, we report on a reversibly switchable fluorescent protein, Tetdron, whose crystals undergo a photo-induced martensitic transformation at room temperature. Room-temperature X-ray crystallography demonstrates that at equilibrium Tetdron chromophores are all in the trans configuration, with an ∼1:1 mixture of their protonated and deprotonated forms. Irradiation of a Tetdron crystal with 400 nm light induces a martensitic transformation, which results in Tetdron tetramerization at room temperature revealed by X-ray photocrystallography. Crystal and solution spectroscopic measurements provide evidence that the photo-induced martensitic phase transition is coupled with the chromophore deprotonation, but no trans-cis isomerization is detected in the structure of an irradiated crystal. It is hypothesized that protein dynamics assists in the light-induced proton transfer from the chromophore to the bulk solvent and in the ensuing martensitic phase transition. The unique properties of Tetdron may be useful in developing novel biomaterials for optogenetics, data storage and nanotechnology.
Original language | English |
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Pages (from-to) | 619-629 |
Number of pages | 11 |
Journal | IUCrJ |
Volume | 6 |
DOIs | |
State | Published - Jul 1 2019 |
Funding
This research used resources of the Advanced Photon Source, a US Department of Energy (DOE) Office of Science User Facility operated for the DOE Office of Science by Argonne National Laboratory under Contract No. DE-AC02-06CH11357. The D2O used in this research was supplied by the United States Department of Energy Office of Science by the Isotope Program in the Office of Nuclear Physics. The Office of Biological and Environmental Research supported research at Oak Ridge National Laboratory’s (ORNL) Center for Structural Molecular Biology (CSMB) involving protein deuteration, using facilities supported by the Scientific User Facilities Division, Office of Basic Energy Sciences, US Department of Energy. Optical measurements were conducted at the ORNL Center for Nanophase Materials Sciences (CNMS) supported by the Scientific User Facilities Division, Office of Basic Energy Sciences, US Department of Energy. This manuscript has been authored by UT-Battelle LLC under DOE Contract No. DE-AC05-00OR22725.
Funders | Funder number |
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Center for Structural Molecular Biology | |
DOE Office of Science | |
ORNL Center for Nanophase Materials Sciences | |
Office of Basic Energy Sciences | |
Office of Nuclear Physics | |
Office of Science User Facility operated | |
Scientific User Facilities Division | |
US Department of Energy | |
UT-Battelle LLC | |
United States Department of Energy Office of Science | |
U.S. Department of Energy | |
Biological and Environmental Research | |
Argonne National Laboratory | |
Oak Ridge National Laboratory | ORNL |
Keywords
- UV-vis absorption spectroscopy
- chromophore deprotonation
- fluorescence
- isomerization
- martensitic transformations
- reversibly switchable fluorescent proteins
- room-temperature X-ray photocrystallography
- tetramerization