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Green-to-Red Photoconvertible Dronpa Mutant for Multimodal Super-resolution Fluorescence Microscopy
Author(s) -
Benjamien Moeyaert,
N. Nguyen Bich,
Elke De Zitter,
Susana Rocha,
Koen Clays,
Hideaki Mizuno,
Luc Van Meervelt,
Johan Hofkens,
Peter Dedecker
Publication year - 2014
Publication title -
acs nano
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.554
H-Index - 382
eISSN - 1936-086X
pISSN - 1936-0851
DOI - 10.1021/nn4060144
Subject(s) - photochromism , photobleaching , fluorescence , microscopy , superresolution , brightness , super resolution microscopy , fluorescence microscope , rational design , fluorescent protein , materials science , photoactivated localization microscopy , fluorescence lifetime imaging microscopy , green fluorescent protein , biophysics , biological system , nanotechnology , chemistry , optics , computer science , artificial intelligence , physics , biology , image (mathematics) , biochemistry , gene
Advanced imaging techniques crucially depend on the labels used. In this work, we present the structure-guided design of a fluorescent protein that displays both reversibly photochromic and green-to-red photoconversion behavior. We first designed ffDronpa, a mutant of the photochromic fluorescent protein Dronpa that matures up to three times faster while retaining its interesting photochromic features. Using a combined evolutionary and structure-driven rational design strategy, we developed a green-to-red photoconvertible ffDronpa mutant, called pcDronpa, and explored different optimization strategies that resulted in its improved version, pcDronpa2. This fluorescent probe combines a high brightness with low photobleaching and photoblinking. We herein show that, despite its tetrameric nature, pcDronpa2 allows for multimodal subdiffraction imaging by sequentially imaging a given sample using both super-resolution fluctuation imaging and localization microscopy.

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