4.7 Article

A fluorescent probe with dual acrylate sites for discrimination of different concentration ranges of cysteine in living cells

期刊

ANALYTICA CHIMICA ACTA
卷 1176, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.aca.2021.338763

关键词

Cysteine; Fluorescent probes; Dual sites; Different concentration ranges; Bioimaging

资金

  1. National Natural Science Foundation of China [22077084]
  2. Guangdong Basic and Applied Basic Research Foundation [2020A1515011564]
  3. Liyuan Outstanding Youth Scholar of Shenzhen University

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A novel probe design strategy utilizing two same reacting groups was proposed in this study, simplifying the synthesis route and minimizing interference from competing species. The probe showed distinguishable fluorescence peak wavelengths towards low and high concentration ranges of Cys, emitting green and blue light respectively. This simpler strategy for sensing different concentration ranges of Cys may inspire more probe design in the future.
Monitoring of cysteine (Cys) is of significant importance for studying Cys-involved biological functions and clinically diagnosing Cys-related diseases. Recently, few fluorescent probes with two different reacting sites were reported to be capable of sensing different concentration ranges of Cys with distinct fluorescence signals, particularly suiting for bioimaging. However, due to relative sophisticated synthesis and moderate selectivity, the applications of these probes were still severely restricted. In this work, we proposed a novel probe design strategy by utilizing two same reacting groups, instead of two different reacting groups, to simplify the synthesis route and minimize the interference from competing species. Same reacting groups in a probe with different steric hindrances could exhibit different reactivities to Cys. This probe showed distinguishable fluorescence peak wavelengths towards low and high concentration ranges of Cys, giving green and blue emissions, respectively. Moreover, this probe was successfully applied for monitoring of Cys concentration in living cells. We believe this work provided a simpler strategy for dual-site fluorescent probes to sense difference concentration ranges of Cys, which may inspire more probe design in future. (c) 2021 Elsevier B.V. All rights reserved.

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