0000000000733170

AUTHOR

Arnout Ceulemans

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Thermal Isomerization Mechanism in Dronpa and Its Mutants.

2016

The photoswitching speed of the reversibly switchable fluorescent proteins (RSFPs) from the family of green fluorescent proteins (GFPs) changes upon mutation which is of direct importance for various high-resolution techniques. Dronpa is one of the most used RSFPs. Its point mutants rsFastLime (Dronpa V157G) and rsKame (Dronpa V157L) exhibit a striking difference in their photoswitching speed. Here the QM/MM on-the-fly string method is used in order to explore the details of the thermal isomerization mechanism. The four principal ways in which isomerization may occur have been scrutinized for each of the three proteins. It has been shown that thermal isomerization occurs via a one-bond-flip…

Protein Conformation alpha-HelicalMutantGreen Fluorescent ProteinsGlycineMolecular Dynamics Simulation010402 general chemistryPhotochemistry01 natural sciencesQM/MMDronpaIsomerismLeucine0103 physical sciencesThermalMaterials ChemistryPoint MutationPhysical and Theoretical Chemistrychemistry.chemical_classification010304 chemical physicsChemistryTemperatureValineChromophoreFluorescence0104 chemical sciencesSurfaces Coatings and FilmsAmino acidKineticsThermodynamicsIsomerizationThe journal of physical chemistry. B
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