Development of cyanine probes with dinitrobenzene quencher for rapid fluorogenic protein labelling.

Autor:	Hori Y; Graduate School of Engineering, Osaka University, Suita, Osaka 565-0871, Japan.; Immunology Frontier Research Center, Osaka University, Suita, Osaka 565-0871, Japan., Hirayama S; Graduate School of Engineering, Osaka University, Suita, Osaka 565-0871, Japan., Kikuchi K; Graduate School of Engineering, Osaka University, Suita, Osaka 565-0871, Japan kkikuchi@mls.eng.osaka-u.ac.jp.; Immunology Frontier Research Center, Osaka University, Suita, Osaka 565-0871, Japan.
Jazyk:	angličtina
Zdroj:	Philosophical transactions. Series A, Mathematical, physical, and engineering sciences [Philos Trans A Math Phys Eng Sci] 2017 Nov 28; Vol. 375 (2107).
DOI:	10.1098/rsta.2017.0018
Abstrakt:	A multicolour protein labelling technique using a protein tag and fluorogenic probes is a powerful approach for spatio-temporal analyses of proteins in living cells. Since cyanine fluorophores have attractive properties for multicolour imaging of proteins, there is a huge demand to develop fluorogenic cyanine probes for specific protein labelling in living cells. Herein, we develop fluorogenic cyanine probes for labelling a protein tag by using a dinitrobenzene fluorescence quencher. The probes enhanced fluorescence intensity upon labelling reactions and emitted orange or far-red fluorescence. Intramolecular interactions between the cyanine fluorophores and the dinitrobenzene quencher led not only to fluorescence quenching of the probes in the free state but also to promotion of labelling reactions. Furthermore, the probes successfully imaged cell-surface proteins without a washing process. These findings offer valuable information on the design of fluorogenic cyanine probes and indicate that the probes are useful as novel live-cell imaging tools.This article is part of the themed issue 'Challenges for chemistry in molecular imaging'. (© 2017 The Author(s).)
Databáze:	MEDLINE
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