4.7 Article

A novel colorimetric and ratiometric fluorescent probe for cysteine based on conjugate addition-cyclization-elimination strategy with a large Stokes shift and bioimaging in living cells

Journal

ANALYTICA CHIMICA ACTA
Volume 1058, Issue -, Pages 136-145

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.aca.2019.01.013

Keywords

Colorimetric; Ratiometric; Fluorescent probe; Cysteine; Bioimaging

Funding

  1. National Natural Science Foundation of China [21765008]
  2. Natural Science Foundation of Guangxi [2017GXNSFBA198178, 2018JJA120021]
  3. Students' Platform for Innovation and Entrepreneurship Training Program [201711838009, 201811838035]
  4. Doctor's Scientific Research Foundation of Hezhou University [HZUBS201509]
  5. Research Project of Hezhou University [2018ZZK02]
  6. Special Fund for Science and Technology Base and Talent of Guangxi [GKAD17195088]
  7. Guangxi Preservation and Deep Processing Research in Fruit and Vegetables Talent Highland Project
  8. Special Fund for Distinguished Experts in Guangxi

Ask authors/readers for more resources

Based on conjugate addition-cyclization reaction of Cys with acrylate and subsequent 1,6-elimination of p-hydroxybenzyl moiety, a novel colorimetric and ratiometric fluorescent probe 1 was designed and synthesized. Upon addition of Cys to the solution of 1, the absorption spectra changed from 508 nm to 452 nm (Delta 56 nm) and afforded visible color change from pink to yellow. Meanwhile, the emission spectra shifted from 644 nm to 539 nm (Delta 105 nm) with remarkable changes in the emission ratio of F-539 nm/F-644 nm (R/R-0 up to 760-fold), accompanying with an obvious fluorescence change from orange to green under illumination with a 365 nm UV lamp. In addition, 1 exhibited a large Stokes shift (136 nm), high sensitivity (detection limit of 46.7 nM), and excellent selectivity to Cys over Hcy and GSH. Moreover, 1 can discriminate Cys from Hcy and GSH by fluorescence spectra, even obvious visible and fluorescence color changes. Importantly, 1 can be used to image Cys in living cells by dual emission channels. (C) 2019 Elsevier B.V. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available