AgHalo: A Facile Fluorogenic Sensor to Detect Drug‐Induced Proteome Stress

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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Angewandte Chemie (International ed.) 2017-07, Vol.56 (30), p.8672-8676
Hauptverfasser: Liu, Yu, Fares, Matthew, Dunham, Noah P., Gao, Zi, Miao, Kun, Jiang, Xueyuan, Bollinger, Samuel S., Boal, Amie K., Zhang, Xin
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung: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. A fluorogenic sensor was developed to detect drug‐induced proteome stress. In contrast to previous sensors, the fluorogenicity enables direct fluorescence readout for facile detection. Differential proteome stress induced by different anticancer drugs was revealed using this assay, but it is invisible to current cytotoxicity assays.
ISSN:1433-7851
1521-3773
DOI:10.1002/anie.201702417