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Modern Fluorescent Proteins: From Chromophore Formation to Novel Intracellular Applications
Author(s) -
Olesya V. Stepanenko,
Olga V. Stepanenko,
Daria M. Shcherbakova,
Irina М. Kuznetsova,
Konstantin К. Turoverov,
Vladislav V. Verkhusha
Publication year - 2011
Publication title -
biotechniques
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.617
H-Index - 131
eISSN - 1940-9818
pISSN - 0736-6205
DOI - 10.2144/000113765
Subject(s) - chromophore , förster resonance energy transfer , fluorescence , fluorescent protein , microscopy , fluorescence microscope , biophysics , nanotechnology , two photon excitation microscopy , palette (painting) , superresolution , green fluorescent protein , fluorescence lifetime imaging microscopy , chemistry , materials science , computer science , biology , optics , photochemistry , physics , biochemistry , artificial intelligence , image (mathematics) , gene , operating system
The diverse biochemical and photophysical properties of fluorescent proteins (FPs) have enabled the generation of a growing palette of colors, providing unique opportunities for their use in a variety of modern biology applications. Modulation of these FP characteristics is achieved through diversity in both the structure of the chromophore as well as the contacts between the chromophore and the surrounding protein barrel. Here we review our current knowledge of blue, green, and red chromophore formation in permanently emitting FPs, photoactivatable FPs, and fluorescent timers. Progress in understanding the interplay between FP structure and function has allowed the engineering of FPs with many desirable features, and enabled recent advances in microscopy techniques such as super-resolution imaging of single molecules, imaging of protein dynamics, photochromic FRET, deep-tissue imaging, and multicolor two-photon microscopy in live animals.

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