| Literature DB >> 28557281 |
Yu Liu1, Matthew Fares1, Noah P Dunham2, Zi Gao2, Kun Miao1, Xueyuan Jiang2, Samuel S Bollinger1, Amie K Boal1,2, Xin Zhang1,2,3.
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.Entities:
Keywords: biosensors; cytotoxicity; fluorescent probes; protein aggregation; proteome stress
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Year: 2017 PMID: 28557281 DOI: 10.1002/anie.201702417
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336