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Selectively monitoring glutathione in human serum and growth-associated living cells using gold nanoclusters

谷胱甘肽 半胱氨酸 纳米团簇 化学 荧光 生物物理学 癌细胞 胶束 生物化学 癌症 生物 医学 有机化学 内科学 物理 水溶液 量子力学
作者
Xiaoxue Xie,Zhenqi Peng,Xinyi Hua,Zhifang Wang,Keqin Deng,Xiumei Yang,Haowen Huang
出处
期刊:Biosensors and Bioelectronics [Elsevier]
卷期号:148: 111829-111829 被引量:39
标识
DOI:10.1016/j.bios.2019.111829
摘要

Glutathione (GSH) plays a variety of vital functions in biological systems. Growth-associated change of GSH level in cells might be critical for cell survival and monitoring of GSH in living cells are of great significance for understanding the dynamic link between GSH and some diseases. In this work, chitason micelles templated gold nanoclusters (CM-Au NCs) emitting red fluorescence were prepared with a simple and rapid method, which shows interesting phenomenon of aggregation induced emission (AIE) affected by the size of the chitosan micelles. The unique CM-Au NCs can be used to develop turn-off fluorescent probe for detecting GSH in human serum and living cells based on the reverse process of AIE of CM-Au NCs, completely different from the principle of aggregation caused quenching (ACQ) effect, which can distinguish GSH from other biothiols (cysteine and homocysteine) and quantitatively detect GSH concentration of human serum in healthy people and cancer patients with high sensitivity. The practical application of fluorescent CM-Au NCs for cellular imaging and detecting GSH level indicates ultra-trace changes of GSH levels in normal and cancer cells could be monitored at different growth stages, which reveals that the levels of GSH in cancer cells was always higher than that of normal cells. Compared with commercial GSH assay kits for detection GSH in human serum and living cells, the proposed method was verified to be accuracy and precision. The results not only reflect the changes of GSH during cell growth at different stages, but also demonstrate the feasibility of reverse process of AIE of CM-Au NCs for detection GSH. This strategy would provide a platform to understand the dynamic link between GSH and disease to clarify the disease mechanism.
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