Citation: YANG Tingting, GUO Zhiqian, SHAO Andong, ZHAO Ping, ZHU Weihong. A Turn-On Fluorescent Probe for Cysteine Based on Benzopyran[J]. Chinese Journal of Applied Chemistry, ;2016, 33(4): 397-405. doi: 10.11944/j.issn.1000-0518.2016.04.160053 shu

A Turn-On Fluorescent Probe for Cysteine Based on Benzopyran

1.
Institute of Fine Chemicals, East China University of Science ＆ Technology, Shanghai 200237, China

Corresponding author: ZHAO Ping,
Received Date: 1 February 2016
Available Online: 2 March 2016
Fund Project:

A benzopyran-based turn-on near-infrared probe (E)-2-(benzopyran)ethenyl-5-(diethylamino)phenyl acrylate(DCM-AC) has been successfully synthesized. Acrylate bond is specifically designed for the response units of amino acid. The results show that the spectral response of DCM-AC towards cysteine is highly sensitivity and selectivity. With increasing the concentration(1.0~8.0 μmol/L) of cysteine, a significant color change can be observed and the fluorescent intensity of DCM-AC at 710 nm increases gradually, showing a good linear relationship with concentration. The limit of detection of DCM-AC for cysteine is determined as 2.8×10^-7 mol/L. DCM-AC exhibits a highly selective probe for cysteine over homocysteine and glutathione, with no interference of other substances. The recognition mechanism of the DCM-AC to cysteine is verified by mass spectrum,¹H NMR titration and absorption spectra, indicating that cysteine thiol groups attack at acrylate double bond of DCM-AC by addition reaction, and finally removed as the cyclic lactam compound.
- cysteine,
- fluorescent probe,
- benzopyran,
- selectivity
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