Simultaneous In Situ Monitoring andImaging of Superoxide Anion, Hydrogen Peroxide, and Protein Phosphorylationfor Early Monitoring of Atherosclerosis

纳米探针 化学 超氧化物 过氧化氢 荧光 生物化学 原位 生物物理学 荧光寿命成像显微镜 分子 活性氧 病理 磷酸化 荧光显微镜 超氧化物歧化酶 分子探针 分子生物学
作者
Ruize Zhao,Jin Li (119007),Wei Zhang (405),Ping Li (31981),Y H Tang,Wen Zhang (7555),Hui Wang (30400),Bo Tang (23472)
出处
期刊: [Figshare (United Kingdom)]
标识
DOI:10.1021/acs.analchem.6c02211.s001
摘要

Investigating the correlation between changes in multiple active molecule levels and the progression of atherosclerosis holds significant practical value for achieving early disease monitoring. To this end, this study constructed a fluorescence nanoprobe for monitoring superoxide anion (O2•–), hydrogen peroxide (H2O2), and protein phosphorylation, which enabled the synchronous detection and imaging of the three molecules at both the cellular and in vivo levels, thereby systematically exploring the correlation between their level changes and early disease progression. Two-photon fluorescence imaging was used to monitor changes in the levels of the three molecules in the aorta of model, which showed that the levels of protein phosphorylation, O2•–, and H2O2 in vascular tissues of the disease group were significantly elevated. More importantly, deep tissue imaging (approximately 140 μm) was achieved utilizing the two-photon imaging. Meanwhile, changes in active molecules in the blood during different disease stages were observed, and as the disease progressed, all three indicators showed a marked increase; among them, hydrogen peroxide exhibits the most pronounced fluorescence response. Serum testing combined with two-photon imaging provides support for early monitoring of atherosclerosis.
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