Issue 48, 2020

A novel “turn-on” fluorescent probe based on naphthalimide for the tracking of lysosomal Cu2+ in living cells

Abstract

A novel fluorescent probe CuNI was synthesized and exhibited highly effective fluorescence detection ability for Cu2+ in aqueous solution (HOAc–NaOAc buffer, 10 mM, pH 5.0). CuNI was obtained by a simple condensation reaction between the aldehyde (MFNI, bearing the naphthalimide fluorescence group) and the 2-picolinyl hydrazide, which bears the Cu2+ recognized group. Under acidic conditions, CuNI showed turn-on fluorescence recognition of Cu2+ which could be readily distinguished with the naked eye under a 365 nm UV lamp and the detection limit is as low as 19.40 nM. It has been further demonstrated that CuNI was hydrolyzed under the action of Cu2+ and the significant increase of fluorescence is due to the obvious AIE effect of the hydrolysate MFNI. The application of the probe CuNI in imaging lysosomal Cu2+ in HepG2 cells has also been demonstrated.

Graphical abstract: A novel “turn-on” fluorescent probe based on naphthalimide for the tracking of lysosomal Cu2+ in living cells

Supplementary files

Article information

Article type
Paper
Submitted
11 Sep 2020
Accepted
14 Nov 2020
First published
16 Nov 2020

New J. Chem., 2020,44, 21167-21175

A novel “turn-on” fluorescent probe based on naphthalimide for the tracking of lysosomal Cu2+ in living cells

T. Xu, J. Huang, M. Fang, M. Sui, Y. Zhu, Y. Shentu, C. Li and W. Zhu, New J. Chem., 2020, 44, 21167 DOI: 10.1039/D0NJ04416D

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