蛋白质组
细胞毒性
程序性细胞死亡
化学
药品
人类蛋白质组计划
蛋白质组学
计算生物学
细胞生物学
生物化学
生物
细胞凋亡
药理学
体外
基因
作者
Yu Liu,Matthew Fares,N.P. Dunham,Zi Gao,Kun Miao,Xueyuan Jiang,Samuel S. Bollinger,Amie K. Boal,Xin Zhang
标识
DOI:10.1002/anie.201702417
摘要
Abstract Drug‐induced proteome stress that involves protein aggregation may cause adverse effects and undermine the safety profile of a drug. Safety of drugs is regularly evaluated using cytotoxicity assays that measure cell death. However, these assays provide limited insights into the presence of proteome stress in live cells. A fluorogenic protein sensor is reported to detect drug‐induced proteome stress prior to cell death. An aggregation prone Halo‐tag mutant (AgHalo) was evolved to sense proteome stress through its aggregation. Detection of such conformational changes was enabled by a fluorogenic ligand that fluoresces upon AgHalo forming soluble aggregates. Using 5 common anticancer drugs, we exemplified detection of differential proteome stress before any cell death was observed. Thus, this sensor can be used to evaluate drug safety in a regime that the current cytotoxicity assays cannot cover and be generally applied to detect proteome stress induced by other toxins.
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