Regulated Fast Nucleocytoplasmic Shuttling Observed by Reversible Protein Highlighting

By R. Ando, H. Mizuno, A. Miyawaki. Science, 2004

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Photoactivatable mCherry for high-resolution two-color fluorescence microscopy (2009, neutral): “5 at 37 1C (min) 23 18 25 NDb 90 (179) (42) (15)”
Far-Field Optical Nanoscopy (2007, background): “Concrete examples of reversible photoswitching are found in reversibly photoactivatable GFP-like proteins, such as asFP595 [106] and dronpa [107], and in photochromic organic compounds.”
Bioimage informatics: a new area of engineering biology (2008, background): “…success of these applications, such as bioimage feature identification, segmentation and tracking, registration, annotation, mining, image data management and visualization, are further summarized, along with a brief overview of the available bioimage databases, analysis tools and other resources.”
Photoactivatable fluorescent proteins (2005, background): “Second, tetrameric PAFPs have been made monomeric by mutagenesis that disrupts the tetramer interface”
Fluorescent proteins and their applications in imaging living cells and tissues. (2010, background): “68, 70), green-to-none “quenchable” Dronpa (16, 139, 140) and a number of its enhanced versions and modifications (14, 17, 414, 486), cyan-to-none “quenchable” mTFP0.”