4.7 Article

Fluorescence imaging of glutathione with aptasensor and monitoring deoxynivalenol-induced oxidative stress in living cells

Journal

SENSORS AND ACTUATORS B-CHEMICAL
Volume 354, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2021.131190

Keywords

Glutathione; Aptasensor; Fluorescence imaging; Deoxynivalenol; Oxidative stress

Funding

  1. National Natural Science Foundation of China [32072310, 31871881, 31772086]
  2. Fundamental Research Funds for the Central Universities [JUSRP221004, JUSRP21826]
  3. National High-level Personnel of Special Support Program [W03020371]
  4. Jiangsu Postdoctoral Research Foundation [2021K305C]

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In this study, an aptamer-based nanoprobe was developed for real-time monitoring of intracellular glutathione (GSH) levels and evaluation of oxidative stress status. The results showed that the nanoprobe had high sensitivity and specificity for GSH, and the limit of detection was low. The study also revealed the saturation point of oxidative stress in living cells induced by deoxynivalenol (DON) concentration.
Glutathione (GSH) is an important intracellular antioxidant. It is closely related to the homeostasis of the intracellular redox state which can be changed through deoxynivalenol (DON) exposure. More importantly, GSH deficiency can directly lead to apoptosis and cellular metabolic disorders mediated by intracellular redox homeostasis. Therefore, real-time monitoring of dynamic changes of GSH levels in living cells is urgently needed for the evaluation of intracellular oxidative stress. Herein, for the first time, an aptamer-based recognition composite nanoprobe (Apt-AuNCs-MoS2) was successfully constructed. The nanoprobe was employed for real-time and in situ imaging of DON-induced intracellular GSH changes and evaluation of oxidative stress status. The results indicated that the aptasensor revealed excellent specificity and high sensitivity to GSH in the solution system, and the limit of detection was as low as 35 nM. The results about DON-mediated oxidative stress indicated that the oxidative stress in living cells tends to be saturated with more than 20 ppm DON concentration. Thus, the strategy provides a novel aptasensor for the determination of GSH, offers a promising platform for fluorescence imaging of intracellular GSH in living cells, and further enriches in situ analysis of the in vitro toxicology.

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