» Articles » PMID: 17384059

Highlighted Generation of Fluorescence Signals Using Simultaneous Two-color Irradiation on Dronpa Mutants

Overview
Journal Biophys J
Publisher Cell Press
Specialty Biophysics
Date 2007 Mar 27
PMID 17384059
Citations 41
Authors
Affiliations
Soon will be listed here.
Abstract

Dronpa absorbs blue light and emits bright green fluorescence. It can also be converted by strong irradiation at 490 nm to a nonfluorescent state, which can then be switched back to the original emissive state with irradiation at 400 nm. Through semirandom mutagenesis studies, we have developed two mutants of Dronpa that show efficient photoswitching kinetics. Compared to Dronpa, the mutants can be turned off by blue light more efficiently. Thus, excitation with an argon laser line (488 nm) makes the mutants quickly become dark such that no substantial fluorescence signals can be observed. Excitation with a violet laser diode (405 nm) also produces no fluorescence signals. Simultaneous 488- and 405-nm irradiation, however, results in a rapid oscillation between the two states, thereby keeping the emissive state population large enough to produce sufficiently bright fluorescence signals.

Citing Articles

The role of the correlated motion(s) of the chromophore in photoswitching of green and red forms of the photoconvertible fluorescent protein mSAASoti.

Gavshina A, Solovyev I, Khrenova M, Boyko K, Varfolomeeva L, Minyaev M Sci Rep. 2024; 14(1):8754.

PMID: 38627478 PMC: 11021400. DOI: 10.1038/s41598-024-59364-1.


Cytoneme signaling provides essential contributions to mammalian tissue patterning.

Hall E, Dillard M, Cleverdon E, Zhang Y, Daly C, Ansari S Cell. 2024; 187(2):276-293.e23.

PMID: 38171360 PMC: 10842732. DOI: 10.1016/j.cell.2023.12.003.


Structural Characterization of Fluorescent Proteins Using Tunable Femtosecond Stimulated Raman Spectroscopy.

Chen C, Henderson J, Ruchkin D, Kirsh J, Baranov M, Bogdanov A Int J Mol Sci. 2023; 24(15).

PMID: 37569365 PMC: 10418586. DOI: 10.3390/ijms241511991.


Resonances at Fundamental and Harmonic Frequencies for Selective Imaging of Sine-Wave Illuminated Reversibly Photoactivatable Labels.

Pellissier-Tanon A, Chouket R, Zhang R, Lahlou A, Espagne A, Lemarchand A Chemphyschem. 2022; 23(23):e202200295.

PMID: 35976176 PMC: 10087976. DOI: 10.1002/cphc.202200295.


Photoswitchable Fluorescent Proteins: Mechanisms on Ultrafast Timescales.

Tang L, Fang C Int J Mol Sci. 2022; 23(12).

PMID: 35742900 PMC: 9223536. DOI: 10.3390/ijms23126459.


References
1.
Sawano A, Miyawaki A . Directed evolution of green fluorescent protein by a new versatile PCR strategy for site-directed and semi-random mutagenesis. Nucleic Acids Res. 2000; 28(16):E78. PMC: 108465. DOI: 10.1093/nar/28.16.e78. View

2.
Sawano A, Hama H, Saito N, Miyawaki A . Multicolor imaging of Ca(2+) and protein kinase C signals using novel epifluorescence microscopy. Biophys J. 2002; 82(2):1076-85. PMC: 1301914. DOI: 10.1016/S0006-3495(02)75467-2. View

3.
Hell S, Dyba M, Jakobs S . Concepts for nanoscale resolution in fluorescence microscopy. Curr Opin Neurobiol. 2004; 14(5):599-609. DOI: 10.1016/j.conb.2004.08.015. View

4.
Stiel A, Trowitzsch S, Weber G, Andresen M, Eggeling C, Hell S . 1.8 A bright-state structure of the reversibly switchable fluorescent protein Dronpa guides the generation of fast switching variants. Biochem J. 2006; 402(1):35-42. PMC: 1783997. DOI: 10.1042/BJ20061401. View

5.
Habuchi S, Ando R, Dedecker P, Verheijen W, Mizuno H, Miyawaki A . Reversible single-molecule photoswitching in the GFP-like fluorescent protein Dronpa. Proc Natl Acad Sci U S A. 2005; 102(27):9511-6. PMC: 1157093. DOI: 10.1073/pnas.0500489102. View