Issue 20, 2014

Fluorescence turn-on detection of Sn2+ in live eukaryotic and prokaryotic cells

Abstract

Sn2+ is usually added to toothpaste to prevent dental plaque and oral disease. However, studies of its physiological role and bacteriostatic mechanism are restricted by the lack of versatile Sn2+ detection methods applicable to live cells, including Streptococcus mutans. Here we report two Sn2+ fluorescent probes containing a rhodamine B derivative as a fluorophore, linked via the amide moiety to N,N-bis(2-hydroxyethyl)ethylenediamine (R1) and tert-butyl carbazate group (R2), respectively. These probes can selectively chelate Sn2+ and show marked fluorescence enhancement due to the ring open reaction of rhodamine induced by Sn2+ chelation. The probes have high sensitivity and selectivity for Sn2+ in the presence of various relevant metal ions. Particularly, both R1 and R2 can target lysosomes, and R2 can probe Sn concentrations in lysosomes with rather acidic microenvironment. Furthermore, these two probes have low toxicity and can be used as imaging probes for monitoring Sn2+ not only in live KB cells (eukaryotic) but also in Streptococcus mutans cells (prokaryotic), which is a useful tool to study the physiological function of Sn2+ in biological systems.

Graphical abstract: Fluorescence turn-on detection of Sn2+ in live eukaryotic and prokaryotic cells

Supplementary files

Article information

Article type
Paper
Submitted
04 Jun 2014
Accepted
21 Jul 2014
First published
21 Jul 2014

Analyst, 2014,139, 5223-5229

Author version available

Fluorescence turn-on detection of Sn2+ in live eukaryotic and prokaryotic cells

H. Lan, Y. Wen, Y. Shi, K. Liu, Y. Mao and T. Yi, Analyst, 2014, 139, 5223 DOI: 10.1039/C4AN01014K

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