蛋白质组
肝损伤
蛋白质组学
化学
蛋白质聚集
计算生物学
细胞生物学
生物
生物化学
药理学
基因
作者
Xuepeng Dong,Zhenduo Zhang,Wang Wan,Biao Jing,Jintai Deng,Wenhan Jin,Di Shen,Zhenming Gao,Yu Liu
出处
期刊:ACS Sensors
[American Chemical Society]
日期:2023-05-30
卷期号:8 (6): 2247-2254
被引量:1
标识
DOI:10.1021/acssensors.3c00216
摘要
Given the extreme heterogeneity and the loss of defined protein structures, misfolded and aggregated proteins are technically challenging to visualize and analyze. Herein, we assembled an integrated sensor system to resolve aggregated proteome in live cells and animal liver tissues that are overdosed by non-steroidal anti-inflammatory drugs (NSAIDs). A fluorogenic protein aggregation sensor (AggStain) first discovered the presence of aggregated proteome upon overdosing liver cells with NSAIDs. A solvatochromic protein aggregation sensor (AggRetina) further quantified the compactness (polarity) inside these cellular aggregates. Importantly, we exploited a proteomic sensor (AggLink) to selectively capture aggregated proteins upon NSAID overdose and profile their composition, revealing global collapse of cellular protein homeostasis. Finally, we detected subtle proteome aggregation in mouse liver tissue without obvious acute injury at a low NSAID dosage. Overall, we demonstrated an integrated sensor toolset for proteome aggregation studies and unveiled for the first time that NSAID overdose can cause proteome aggregation in liver cells and tissues.
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