4.7 Article

In situ and dynamic SERS monitoring of glutathione levels during cellular ferroptosis metabolism

Journal

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
Volume -, Issue -, Pages -

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-023-04909

Keywords

Surface-enhanced Raman scattering; Glutathione; Ferroptosis; Nanoprobe

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An excellent plasmonic nanoprobe was developed for real-time monitoring of intracellular GSH levels during ferroptosis. The nanoprobe, consisting of gold nanoparticles functionalized with crystal violet, detects GSH through the fluctuation in the SERS signal intensity. This low-cost, stable, and biocompatible nanoprobe enables dynamic monitoring of GSH levels in living cells during erastin-induced ferroptosis.
Ferroptosis is a non-apoptotic cell death regulated by iron-dependent lipid peroxidation. Glutathione (GSH), a key antioxidant against oxidative damage, is involved in one of the most important metabolic pathways of ferroptosis. Herein, an excellent plasmonic nanoprobe was developed for highly sensitive, in situ, dynamic real-time monitoring of intracellular GSH levels during ferroptosis. A nanoprobe was prepared by functionalizing gold nanoparticles (AuNPs) with the probe molecule crystal violet (CV). The fluctuation in the SERS signal intensity of CV via the competitive displacement reaction can be used to detect GSH. The advantages of the plasmonic nanoprobe including low-cost production techniques, outstanding stability and biocompatibility, high specificity and sensitivity towards GSH with a detection limit of 0.05 & mu;M. It enables real-time dynamic monitoring of GSH levels in living cells during erastin-induced ferroptosis. This approach is expected to provide important theoretical support for elucidating the GSH-related ferroptosis metabolic mechanism and advancing our understanding of ferroptosis-based cancer therapy.

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