4.7 Article

A fluorescent probe for monitoring Cys fluctuations in the oxidative stress environment simulated by Cu2+ or H2O2

期刊

BIOORGANIC CHEMISTRY
卷 120, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bioorg.2022.105618

关键词

Fluorescent probe; Cys; Oxidative stress; Biological imaging

资金

  1. National Natural Science Foundation of China [21472118, 21672131]
  2. Program for the Top Young and Middle-aged Innovative Talents of Higher Learning Institutions of Shanxi [2013802]
  3. Talents Support Program of Shanxi Province [2014401]
  4. Shanxi Province Outstanding Youth Fund [2014021002]
  5. Natural Science Foundation of Shanxi Province of China [201701D121018]

向作者/读者索取更多资源

Redox balance is crucial for maintaining a healthy physiological state. Cysteine, an important biomolecule, plays an indispensable role in this process. In this study, a fluorescent probe NF-O-SBD was designed to specifically detect cysteine, and its practical application was demonstrated in biology.
Redox balance is the core of holding the good physiological state of the body. Cysteine (Cys) is one of the important biomolecules, which plays an indispensable role in maintaining the body's redox homeostasis. The redox of organisms is mainly the result of the dynamic balance between reactive oxygen species (ROS) and biological reducing agents (such as Cys). Fluorescent probes have the advantages of simple operation, good specificity and high sensitivity, and have become a common tool for bio-sensing in complex systems. In this article, we designed a probe NF-O-SBD that can specifically detect Cys. The chlorine atom of NF-O-SBD was easily substituted by sulfhydryl as a reaction site. After the formation of sulfur substitution products, intramolecular rearrangement occurred and fluorescent signal was emitted in the yellow channel at 550 nm. It can be seen from the spectroscopy experiment that the content of Hcy in organisms (15 mu M) basically did not cause significant fluorescence changes, Therefore, based on the practical application in biology, we further used NF-OSBD to visualize endogenous and exogenous Cys in HepG-2 cells and zebrafish. Simultaneously, we used Cu2+ or H2O2 induction to simulate the oxidative stress environment of cells and zebrafish, under which the concentration variation of Cys was monitored.

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